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Stem Cell Assay Market Growth By Manufacturers, Countries, Types And Application, End Users And Forecast To 2026 – 3rd Watch News

Posted: July 9, 2020 at 2:47 am

New Jersey, United States,- Verified Market Research sheds light on the market scope, potential, and performance perspective of the Stem Cell Assay Market by carrying out an extensive market analysis. Pivotal market aspects like market trends, the shift in customer preferences, fluctuating consumption, cost volatility, the product range available in the market, growth rate, drivers and constraints, financial standing, and challenges existing in the market are comprehensively evaluated to deduce their impact on the growth of the market in the coming years. The report also gives an industry-wide competitive analysis, highlighting the different market segments, individual market share of leading players, and the contemporary market scenario and the most vital elements to study while assessing the Stem Cell Assay market.

The research study includes the latest updates about the COVID-19 impact on the Stem Cell Assay sector. The outbreak has broadly influenced the global economic landscape. The report contains a complete breakdown of the current situation in the ever-evolving business sector and estimates the aftereffects of the outbreak on the overall economy.

Leading Stem Cell Assay manufacturers/companies operating at both regional and global levels:

The report also inspects the financial standing of the leading companies, which includes gross profit, revenue generation, sales volume, sales revenue, manufacturing cost, individual growth rate, and other financial ratios.

Industrial Analysis:

The Stem Cell Assay market report is extensively categorized into different product types and applications. The study has a separate section for explaining the cost of raw material and the revenue returns that are gained by the players of the market.

The segmentation included in the report is beneficial for readers to capitalize on the selection of appropriate segments for the Stem Cell Assay sector and can help companies in deciphering the optimum business move to reach their desired business goals.

In Market Segmentation by Types of Stem Cell Assay, the report covers-

Bytype1

In Market Segmentation by Applications of the Stem Cell Assay, the report covers the following uses-

Byapplication1

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The Stem Cell Assay market report provides successfully marked contemplated policy changes, favorable circumstances, industry news, developments, and trends. This information can help readers fortify their market position. It packs various parts of information gathered from secondary sources, including press releases, web, magazines, and journals as numbers, tables, pie-charts, and graphs. The information is verified and validated through primary interviews and questionnaires. The data on growth and trends focuses on new technologies, market capacities, raw materials, CAPEX cycle, and the dynamic structure of the Stem Cell Assay market.

This study analyzes the growth of Stem Cell Assay based on the present, past and futuristic data and will render complete information about the Stem Cell Assay industry to the market-leading industry players that will guide the direction of the Stem Cell Assay market through the forecast period. All of these players are analyzed in detail so as to get details concerning their recent announcements and partnerships, product/services, and investment strategies, among others.

Sales Forecast:

The report contains historical revenue and volume that backing information about the market capacity, and it helps to evaluate conjecture numbers for key areas in the Stem Cell Assay market. Additionally, it includes a share of each segment of the Stem Cell Assay market, giving methodical information about types and applications of the market.

Reasons for Buying Stem Cell Assay Market Report

This report gives a forward-looking prospect of various factors driving or restraining market growth.

It renders an in-depth analysis for changing competitive dynamics.

It presents a detailed analysis of changing competition dynamics and puts you ahead of competitors.

It gives a six-year forecast evaluated on the basis of how the market is predicted to grow.

It assists in making informed business decisions by performing a pin-point analysis of market segments and by having complete insights of the Stem Cell Assay market.

This report helps the readers understand key product segments and their future.

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In the end, the Stem Cell Assay market is analyzed for revenue, sales, price, and gross margin. These points are examined for companies, types, applications, and regions.

To summarize, the Stem Cell Assay market report studies the contemporary market to forecast the growth prospects, challenges, opportunities, risks, threats, and the trends observed in the market that can either propel or curtail the growth rate of the industry. The market factors impacting the global sector also include provincial trade policies, international trade disputes, entry barriers, and other regulatory restrictions.

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Stem Cell Assay Market Growth By Manufacturers, Countries, Types And Application, End Users And Forecast To 2026 - 3rd Watch News

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Tremendous growth report on Stem Cell Market 2020-2028 Enhanced Growth, Recent Trends and Major Companies are Thermo Fisher Scientific, Qiagen NV,…

Posted: July 9, 2020 at 2:47 am

Stem Cell Market is analyzed with industry experts in mind to maximize return on investment by providing clear information needed for informed business decisions. This research will help both established and new entrants to identify and analyze market needs, market size and competition. It explains the supply and demand situation, the competitive scenario, and the challenges for market growth, market opportunities and the threats faced by key players.

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A 360 degree outline of the competitive scenario of the Global Stem Cell Market is presented by Quince Market Insights. It has a massive data allied to the recent product and technological developments in the markets.

It has a wide-ranging analysis of the impact of these advancements on the markets future growth, wide-ranging analysis of these extensions on the markets future growth. The research report studies the market in a detailed manner by explaining the key facets of the market that are foreseeable to have a countable stimulus on its developing extrapolations over the forecast period.

Companies Covered:Thermo Fisher Scientific, Qiagen NV, Sigma Aldrich, Becton, Dickinson and Company, and Stem Cell Technologies

Table of Contents:

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Market Segmentation: By Source (Adult Stem Cell, Human Embryonic Cell, Pluripotent Stem Cell, and Others), By Application (Therapeutic and Drug Development and Discovery), By Treatment Type (Allogeneic, Autologous, and Syngeneic), By Stem Cell Banking (Service & Technology and Banking Type)

A detailed outline of the Global Stem Cell Market includes a comprehensive analysis of different verticals of businesses. North America, Europe, Asia Pacific, Middle East & Africa, and South America have been considered for the studies on the basis of several terminologies.

This is anticipated to drive the Global Stem Cell Market over the forecast period. This research report covers the market landscape and its progress prospects in the near future. After studying key companies, the report focuses on the new entrants contributing to the growth of the market. Most companies in the Global Stem Cell Market are currently adopting new technological trends in the market.

Finally, the researchers throw light on different ways to discover the strengths, weaknesses, opportunities, and threats affecting the growth of the Global Stem Cell Market. The feasibility of the new report is also measured in this research report.

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Tremendous growth report on Stem Cell Market 2020-2028 Enhanced Growth, Recent Trends and Major Companies are Thermo Fisher Scientific, Qiagen NV,...

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Global Musculoskeletal Disorder Stem Cell Therapy Market 2020 by Company, Regions, Type and Application, Forecast to 2025 – Daily Research Chronicles

Posted: July 9, 2020 at 2:47 am

Global Musculoskeletal Disorder Stem Cell Therapy Market 2020 by Company, Regions, Type and Application, Forecast to 2025 added by Researchstore.biz unveils the current & future growth trends of this business and outlines details regarding the developments of the market. The report analyzes geographies that form a part of the regional spectrum of the global Musculoskeletal Disorder Stem Cell Therapy market. While offering a complete study of the micro and macroeconomic aspects of the market, the report also emphasizes the key driving and restraining forces for this market. The report then sheds light on the supply & demand analysis, contributions by the top players, and market share growth statistics of the industry.

Market Overview:

The report contains an exhaustive analysis of this business space, along with a succinct overview of its various market segments. A basic overview of the Musculoskeletal Disorder Stem Cell Therapy market has been offered with respect to its present position and the industry size, based on revenue and volume. The Global Musculoskeletal Disorder Stem Cell Therapy Market Report has used analytical tools to include accurate research and evaluation data on key industry players and market coverage. Key elements regarding top companies such as their classification, size, profiles, business atmosphere, future, and recent trends, and contact information are featured in the report. Moreover, data concerning growth opportunities for the market across every detailed region is included in the report. The anticipated growth rate expected to be recorded by each region over the estimated years (2020-2025) has also been given within the research report.

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NOTE: This report takes into account the current and future impacts of COVID-19 on this industry and offers you an in-dept analysis of Musculoskeletal Disorder Stem Cell Therapy market.

The report investigates the development, trends, and new entrants in the sector, with elaborate profiles of the leading companies operating in the market, including: Osiris Therapeutics , Medi-post , NuVasive , Takeda (TiGenix)

In market segmentation by types, the report covers: Allogeneic, Autologous

In market segmentation by applications, the report covers the following uses: Muscle disease, Skeletal disease

Providing a brief of the regional landscape:

Regional segmentation: North America (United States, Canada and Mexico), Europe (Germany, France, United Kingdom, Russia and Italy), Asia-Pacific (China, Japan, Korea, India, Southeast Asia and Australia), South America (Brazil, Argentina), Middle East& Africa (Saudi Arabia, UAE, Egypt and South Africa)

Moreover, the report talks about the production aspect, product remuneration, the gross margins of the firms manufacturing the product, and the manufacturing of the product. The report includes information about the product consumption volume and the product consumption value has also been given in the global Musculoskeletal Disorder Stem Cell Therapy report. It delivers a detailed understanding of the consumption patterns of the product.

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Global Musculoskeletal Disorder Stem Cell Therapy Market 2020 by Company, Regions, Type and Application, Forecast to 2025 - Daily Research Chronicles

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This Company Wants to Rewrite the Future of Genetic DiseaseWithout Crispr Gene Editing – WIRED

Posted: July 8, 2020 at 3:58 am

That can spell real trouble for the bacteria on the receiving end of this gene shuffle. If those MGEs insert themselves into critical gene regions, its bye-bye bacteria. You can think about MGEs the same way you can think about mutations, says Peters. We wouldnt have evolved without them, but 99.99999 percent of them are bad. Bacteria are trying at any cost to stop MGEs from destabilizing their genome.

The Nobel Prize-winning botanist Barbara McClintock discovered the first known class of MGEs, called transposons, or jumping genes, in maize in 1931. Her technique for staining the plants chromosomes allowed her to see when chunks from one would jump to another. But for many decades, the purpose of all these repeated sections of self-rearranging DNA eluded scientists. Some went so far as to dub the MGE-heavy sections of the human genome junk DNA. It was hard to get funding to study it. But little by little, researchers like Peters discovered that MGEs in bacteria were actually highly-evolved systems for recognizing DNA, writing it, and moving it around. In fact, Crispr itself appears to have evolved from a self-synthesizing transposon, as NIH researchers Eugene Koonin and Kira Makarova described in 2017. (Crispr codes for a protein that cuts specific, recognizable pieces of DNA stored in its genetic memory bank. The transposons allowed Crispr to start amassing that memory bank in the first place.)

Earlier that year, Peters and Koonin published a paper describing how this evolution can sometimes come full circle. They found one type of transposon that had stolen some Crispr genes to help it move between bacterial hosts. They realized that these molecular tools for cutting, copying, and pasting were constantly being shuttled between MGEs, phages, and bacteria to be used alternately as a means of offense or defense. At the end of that paper, Peters and Koonin wrote that these systems could potentially be harnessed for genome-engineering applications.

Not long after, Peters says, he started getting calls from commercial interests. One of them was from Jake Rubens, Tesseras Chief Innovation Officer and co-founder. In 2019, the company began a sponsored research collaboration with Peters Cornell lab around the discovery of new MGEs with genome engineering potential. (Tessera also has other research partnerships, but company officials have not yet disclosed them.)

MGEs come in a few flavors. There are transposons, which can cut themselves out of the genome and hop into a different neighborhood. Retrantransposons make a copy and shuttle that replica to its new home, expanding the size of the genome with each duplication. They both work by having special sequences on either end that define their boundaries. In between are genes for making proteins that recognize those boundaries and either excise them out in the case of transposons, leaving a gap. Or in the case of retrotransposons, copy them, via an RNA-intermediate, into new locations. There are other classes, too, but these are the two that Tessera executives are interested in. Thats because you can add a new string of code between those sequencessay a healthy, non-mutated version of a disease-causing geneand let the MGEs machinery do the work to move that therapeutic DNA into a patients chromosomes.

For the past two years, the companys team of bioinformaticians have been mining public databases that house the genome sequences of hundreds of thousands of bacterial species that scientists have collected from all over the world. In those reams of genetic data, theyve been prospecting for MGEs that might be best suited for making these kinds of therapeutic DNA changes.

So far, company scientists have identified about 6,000 retrotransposons (what Tessera calls RNA writers) and 2,000 transposons (DNA writers) that show potential. Tesseras team of 35 scientists have been conducting experiments in human cells to understand how exactly each one works. Sometimes, a promising, naturally-occurring gene writer will get tweaked further in Tesseras lab, to be more precise or go to a different location. The company hasnt yet demonstrated that any of its gene writers can eliminate an inherited disease. But in mouse models, the team has consistently been able to use them to insert lots of copies of a large green fluorescent protein gene into the animals genomes as a way of proving that they can reliably place designer DNA.

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This Company Wants to Rewrite the Future of Genetic DiseaseWithout Crispr Gene Editing - WIRED

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Perspective on Pharma: Moving from academia to industry – EPM Magazine

Posted: July 8, 2020 at 3:58 am

In this Perspective on Pharma feature, Jung Doh, market development scientist at Beckman Coulter Life Sciences, explains how they entered the pharmaceutical industry after an unexpected opportunity arose.

As an early career scientist with a good number of years of graduate and post-doctoral training (two post-docs, actually), I made an unexpected leap: from academiawhere I thought I would spend my entire professional lifeto industry. And though it wasnt a move Id initially planned, Im the first to say that Im incredibly happy to have ended up here, since its afforded me research and personal growth opportunities I didnt even know I wanted.

After I received my doctorate in biology, I completed a post-doc in HIV research and a second, NASA-funded post-doc in the effects of microgravity on genomes. My dreamand a very concrete goal for many yearswas to become a professor at a research university, running my own lab in an area I was passionate about.

But then life intervened: my wife was offered a teaching position in Indianapolis that she couldnt pass up, so we relocated. After a few months of fruitless application to teaching and research positions at local universities, I started looking elsewhere. There are a lot of pharma and biotech companies in Indianapolis, so I started exploring some of them. In the interview process, (and much to my surprise), I discovered that they shared many of the same passions and goals I did: to benefit human health and life in fundamental and lasting ways.

The company where I ended up and still work, Beckman Coulter Life Sciences, was particularly interesting to me, since one of their key focuses was on next generation sequencing (NGS). Toward the end of my Ph.D. and in my post-doc training, NGS was becoming more routine, and I was fortunate to be able to learn and apply the techniques in my own research.

So I joined Beckman Coulter Life Sciences, which offers a range of scientific research instruments used to study complex biological problems and to advance scientific breakthroughs, first as a marketing application scientist, and then expanding into a dual role as application scientist and proof of principle scientist. In the latter, I worked with customers to develop modified protocols and tools to help research be done more efficiently. I then became product manager for our genomics product line, and as of this year, I have yet another new role, as market development scientist. In this role, I engage with the scientific community to learn from them, as well as support them to perform research better, faster, and with superior results and outcomes. I also bring the learnings and techniques gained from these collaborations to create collateral to offer other labs, or help our internal team develop product offerings for a specific need.

After making the leap into industry, I never looked back. There are, of course, benefits to both sectors. In academia, theres a certain degree of freedom and job securityonce youre tenured, that is. But it takes a lot to get tenured these daysthe funding and grants and a constant stream of publicationsparticularly in biology and related disciplines.

Though industry may seem more constrained at first glance, in many ways, theres as much or more opportunity, since there are a plethora of techniques to learn and apply in novel ways. And since technology evolves so rapidly, especially in genetic engineering and diagnostics, it seems like there are always new methods to master.

Related to this aspect, and alluded to earlier, is the strong sense that my and my colleagues work is genuinely translating into helping people across the globe. I got an inkling of that in the interview process, but its also been a palpable part of my work here. With the current pandemic, for instance, the company came together, and, within a matter of weeks, we were able to offer labs RNA extraction solutions for the virus, which are so critical right now. I felt honoured to be part of a company doing such great work, with flexibility and speed. It definitely speaks to the versatility of the industry.

Beyond the scientific, Ive learned about areas seemingly outside of science, but that are actually integral parts of the business. When I was product manager, for instance, I learned how to manage people, run meetings, build financial models, approach marketing and sales, and many other facets of the business. I had no formal business training going in, but you learn by doing, from your manager and peers. I ended up really loving all these other parts of the business of sciencetheyre challenging, but incredibly rewarding, because they push you beyond your comfort zone into uncharted areas. For that, industry has opened up areas that I didnt even know would be important, let alone fun and rewarding.

Finally, Ive been surprised and heartened by the strong sense of family that exists within a company. Part of this is felt through the opportunities for development, which is evident in all the stages I went through and all the roles Ive had. Theres a sense that staff are supported to grow as scientists and as people, which has made my accidental leap into industry all the more fulfilling.

For young scientists, theres a lot to think about when making decisions about what to study and what track to follow. I would encourage people to not get too hung up on tracks, but to stay open to the possibilitiesin other words, dont get too stuck on academia as the only option just because its where youve done your training. What really matters is having a passion for what you do, and following your interests. Genetic engineering is an area thats exploded in recent years, and will likely grow in the coming years. Ive been lucky that my own work has translated so tangibly into helping people, and at a large scalebut the same is true for many other areas in medical science. So carry onyou may end up in a totally different place from where you started, and thats not a bad thing at all.

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Perspective on Pharma: Moving from academia to industry - EPM Magazine

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Global CRISPR And CRISPR-Associated (Cas) Genes Market 2020 with COVID-19 After Effects Analysis by Key Players Caribou Biosciences, Addgene, CRISPR…

Posted: July 8, 2020 at 3:58 am

CRISPR And CRISPR-Associated (Cas) Genes Industry Overview Competitive Analysis, Regional and Global Analysis, Segment Analysis, Market Forecasts 2026

The new report on the globalCRISPR And CRISPR-Associated (Cas) Genes marketpublished by theMarket Research Storeincorporates all the essential facts about the CRISPR And CRISPR-Associated (Cas) Genes market. This aids different industry players along with new market entrants to open new gateways for the CRISPR And CRISPR-Associated (Cas) Genes market on a global platform. Through in-depth research and data obtained from the reliable database the qualitative and the quantitative data of the CRISPR And CRISPR-Associated (Cas) Genes market has been updated based on the current market conditions owing toCOVID-19. The overall market conditions have been affected due to the pandemic. The trading conditions and the economy crisis have affected the CRISPR And CRISPR-Associated (Cas) Genes market. The information in the CRISPR And CRISPR-Associated (Cas) Genes market report is updated and precise thus the clients will be able to relate themselves to the current market scenario.

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The CRISPR And CRISPR-Associated (Cas) Genes market report also encompasses the details about all the market players that are operating in the CRISPR And CRISPR-Associated (Cas) Genes market. The market players includeCaribou Biosciences, Addgene, CRISPR THERAPEUTICS, Merck KGaA, Mirus Bio LLC, Editas Medicine, Takara Bio USA, Thermo Fisher Scientific, Horizon Discovery Group, Intellia Therapeutics, GE Healthcare Dharmacon.

The market analysis in the CRISPR And CRISPR-Associated (Cas) Genes market study starts with the market definition and scope. In the next section, there is a brief discussion about the target audience of the market. In the later section, a detailed information about the market growth factors and limitations are discussed along with the market opportunities and challenges that are being faced owing to arise of the pandemic. Research tools and methodologies were used while analyzing the CRISPR And CRISPR-Associated (Cas) Genes market.

Read Detailed Index of full Research Study at::http://www.marketresearchstore.com/report/global-crispr-and-crispr-associated-cas-genes-market-608839

The major section that covers the overall market description is the market segmentation. The CRISPR And CRISPR-Associated (Cas) Genes market includes segments{Genome Editing, Genetic engineering, gRNA Database/Gene Librar, CRISPR Plasmid, Human Stem Cells, Genetically Modified Organisms/Crops}; {Biotechnology Companies, Pharmaceutical Companies, Academic Institutes, Research and Development Institutes}. To study any market in detail the major components that need to be analyzed are its product type, application, end-use, the solution and the services that are offered. Details about all these segments helps better understand the market size and demand. Every aspect of every single segment was studied carefully and the impact of COVID-19 was also taken into consideration. Both numerical data and subjective information about every segment is included for better understanding. The regional presence of the CRISPR And CRISPR-Associated (Cas) Genes market is also included. The current market condition in each regions is explained thoroughly as to how the pandemic has affected the CRISPR And CRISPR-Associated (Cas) Genes market demand in a particular region.

Major Advantages for CRISPR And CRISPR-Associated (Cas) Genes Market:

1. Well-organized description of the international CRISPR And CRISPR-Associated (Cas) Genes market along with the ongoing inclinations and future considerations to reveal the upcoming investment areas.2. The all-inclusive market feasibility is examined to figure out the profit-making trends to obtain the most powerful foothold in the CRISPR And CRISPR-Associated (Cas) Genes industry.3. The CRISPR And CRISPR-Associated (Cas) Genes market report covers data which reveal major drivers, constraints, and openings with extensive impact analysis.4. The current market is quantitatively reviewed from 2019 to 2028 to pinpoint the monetary competency of the global CRISPR And CRISPR-Associated (Cas) Genes market.5. Last but not least, PORTERS Five Forces Analysis shows the effectiveness of the customers and providers from a global perspective.

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Global CRISPR And CRISPR-Associated (Cas) Genes Market 2020 with COVID-19 After Effects Analysis by Key Players Caribou Biosciences, Addgene, CRISPR...

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Yeast Market Trend, CAGR Status, Growth, Analysis and Forecast to 2028 – 3rd Watch News

Posted: July 8, 2020 at 3:58 am

Brewing or beer making represents a massive and highly lucrative sector. According to a study, global alcohol consumption has constantly been on the rise, and the consumption of beer accounts for the highest volume share. Yeast, being the cardinal ingredient used in the production of beer, provides the right proportion of texture and flavor to beer during its production. As a result, increasing demand and consumption of beer has been elevating the globalyeast market, which is anticipated to grow at a CAGR of 5.4% during the forecast period 2018-2026. The market valuation has been estimated to be over US$ 10,200 Mn by 2026 end.

Yeast Innovation: The Future of Brewery

The brewing industry has overcome a slew of challenges and moved beyond times when technological breakthroughs were not applied to the beer crafting process. According to a research, one small, low-capital innovation, within the reach of all beer makers is enhancing and improvising the yeast they use in their beer. Even though yeast is partially responsible for imparting the flavor and aroma to beer, brewers often compare yeast to hops. This leaves yeasts dynamic nature untapped, which can be used for product enhancements.

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Research has shown that non-GMO development techniques such as selective breeding can be used to optimize the brewing strains. Ultimately, brewers can enhance the quality of beer by innovative yeast that can be fully customized pertaining to the brewery and its beer with the specific desired parameters in fermentation performance, processing, storage, flavor, and aroma, without compromising quality or brand identity.

Alternatives to Traditional Straining to Drive Innovation in Yeast Market

Studies on the beer and yeast market have pointed at various possibilities that would drive the use of yeast in beer making. For instance, to develop brewers yeast, market players could use hop-accentuating enzymes in high volume which will change the aroma and flavor profiles of the different hop varieties used in beer. Additionally, brewers can add a trait to increase fermentation temperature ranges which would produce desired flavor profiles at lower temperatures, eliminating the problem of off odors that occur at higher temperatures.

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Genetically Engineered Yeast to Offer Excellent Taste to Beer

From great-tasting to cloudy and off-taste beers, yeast accounts for up to a third of a brews final flavor. Brewing yeast has its own genetic limitations. For researchers across the globe, brewing yeast is at the forefront of genetic research and synthetic biology, which is pushing the boundaries of genetic engineering. Geneticists can now tweak the genetic code of brewing yeast to suppress or express certain beer characteristics. From taking out the gene responsible for the butter-flavored molecule diacetyl to using specific gene for banana and clove flavors made by hefeweizen yeast brewers would now be able to use this ability of genetically modified (GM) yeast for the production of beer.

Whether it is straining of yeast or making use of genetically engineered yeast, increased consumption of alcoholic beverages in the world, with beer leading the consumption segment, has witnessed several yeast innovations in recent years, favoring the market growth. For more insights, speak to our expert food analysts at Persistence Market Research to know more about the yeasts market and its impact on the end-user industry.

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Yeast Market Trend, CAGR Status, Growth, Analysis and Forecast to 2028 - 3rd Watch News

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Engineering plants to withstand drought and tolerate salinity – Anthropoce

Posted: July 8, 2020 at 3:58 am

Researchers have managed to engineer plants with bigger cells that can store more watergetting them to behave like water-harboring succulents that thrive in deserts around the world. Whats more, this trait could be widely transferred to agricultural crops, a new study finds.

The discovery, detailed in The Plant Journal, hinges on a gene thats found in wine grapes, called VvCEB1, which causes the cells of the fruit to enlarge during development. When the researchers bred that gene into thale cressa plant widely used as an experimental model in researchthey were able to over-express it, which led the plants to develop unusually large cells, capable of storing larger quantities of water. The plants could not only withstand extremely dry conditions, but were also able to tolerate higher salinity in the soil, the researchers found.

In fact, when exposed to drought-like conditions in the experiment, they showed that only 16 to 25% of the regular thale cress plantswhich lacked the over-expressed VvCEB1 geneultimately survived. The difference in the engineered plants was striking: between 91 and 94% of them survived the dire conditions and continued to grow.

Compared to the non-engineered control plants, the engineered cress were found to retain much more waterand the pace at which they lost water was also notably slower than in the controls, the experiments showed.

Presumably, some of this was thanks to their new, larger cells, which act efficiently like a reservoir in times of need. But the researchers discovered that as well as larger cells, the VvCEB1-expressing plants also had fewer and smaller stomata on their leaves. Especially under dry conditions, water transpires out of stomata at a rapid paceso having fewer and smaller portals to the outside world helps them to keep more water locked in.

On top of all this, the engineered thale cress plants had another advantage over their regular counterparts: equipped with larger cells, these plants became more salt-tolerant, the experiments showed. Thats likely because bigger, more watery cells would help the plant dilute salt thats absorbed from saline soils, as the researchers explain. And whats more, the engineered cress had larger leaves and produced more seeds than the controlsuggesting that productivity isnt sacrificed by this particular genetic tweak.

Interestingly, the researchers made this discovery while pursuing a different research goal. Theyd been trying to engineer plants to contain a trait known as crassulacean acid metabolism (CAM), a naturally-occurring feature in some plants that helps them conserve more water by photosynthesizing only at nightwhen its cooler and safer for stomata to be open. To enable this trait, the researchers needed to engineer plants that contained what they call the right leaf anatomy: namely, larger cells in which to store an ingredient called malic acid, which plays a crucial role in enabling the unusual photosynthetic response. It just so happens that the larger cell sizes which serve that purposes could double up as storage space for water, too.

Altogether, the researchers efforts resulted in the model of a plant that could potentially be drought-tolerant and more adaptable in the higher-salinity landscapes that are expected to expand under climate change.Water-storing tissue is considered among the most successful adaptations to drought in the plant kingdom, the researchers write. And yet, its been largely unexplored as a way to bolster crops against the effects of climate change, they add.

They aim to change that: next up, theyll be combining their discoveries on CAM and reservoir cells, and trying to engineer them jointly into crops.

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COVID-19 Research: Women Are Changing the Face of the Pandemic – Genetic Engineering & Biotechnology News

Posted: July 8, 2020 at 3:58 am

The pristine X-ray crystallography data gathered by Rosalind Franklin played a crucial role in the discovery of DNAs structure. Yet when the discovery was recognized by the Nobel Committee in 1962, the winners of the Nobel Prize did not include Franklin, who had died in 1958. Only recently has Franklin received some of the recognition that she deserves for her essential contribution to one of the biggest discoveries of the past century.

We still have a lot of work to do, unfortunately, notes Akiko Iwasaki, PhD, an immunologist at Yale School of Medicine and a fierce advocate for women in science. Things have definitely gotten better since [Franklins] days she tells GEN. But we still have a huge disparity in women representationespecially at the senior level. Iwasaki adds that we have to address what she thinks is the root cause of the problemthe academic culture and the unconscious (or conscious) bias against women and people of color that prevents these brilliant people from moving up the academic ladder.

To mark the centenary of Franklins birth, GEN sought to highlight scientists at the forefront of COVID-19 researchsome of the most influential research currently being conductedwho are women. In this article, GEN speaks with researchers who are leading efforts to track SARS-CoV-2 genomes, to uncover host factors influencing COVID-19 progression, to develop saliva-based COVID-19 tests, and more.

Working as a pediatrician in China, Qian Zhang, MD, wanted to understand why some children are more susceptible to infections than others. Children are exposed to hundreds of pathogens every day, Zhang tells GEN, but only a very small proportion get really severe infections. Zhang has been researching differences in susceptibility for the past decade. Notably, she performed postdoctoral work at the National Institute of Allergy and Infectious Diseases (NIAID) with Helen Su, MD, PhD. Afterward, Zhang became a postdoctoral fellow at the Rockefeller University, in the laboratory of Jean-Laurent Casanova, MD, PhD.

Working with patient samples, researchers in the Casanova laboratory look for rare, deleterious mutations that might govern susceptibility to infection. In particular, they look for monogenic variants, where a single defect makes an individual far more susceptible to infection. Zhangs hypothesis for COVID-19 is that patients who are susceptible to less virulent respiratory pathogens will also be susceptible to COVID-19. By taking an unbiased approach, Zhang and colleagues may find genetic factors that have never been identified before.

Normally, Zhang analyzes children because it is in childhood that people usually experience infection for the first time. But COVID-19 is different, she notes, because this infection is the first time for everyone.

Zhang previously led the influenza team in the Casanova laboratory. So, taking on COVID-19 is a natural shift. She adds that many commonalities between the two lung infections have been established, and that many tools developed for flu research can be used in COVID-19 work. Besides, there simply arent any more flu patients coming in.

Zhang asserts that her group, like others, has adapted its work to the pandemic. Investigators normally work on well-defined infections. COVID-19, however, isnt so well defined. Too little about it is known. For example, without key pieces of data such as a fatality rate, investigators who look for genetic lesions may be unaware of the lesions prevalence. We have to change our analysis while the data are coming in, Zhang explains.

How much hesitation did Akiko Iwasaki, PhD, have in moving into COVID-19 research? None, she says. I knew the importance of speed and urgency. She notes that she had learned the value of these attributes from her experience jumping into Zika.

Iwasaki, a professor of immunobiology and molecular, cellular, and developmental biology at the Yale School of Medicine and an investigator at the Howard Hughes Medical Institute, has spent the past few months trying to understand the immune response of COVID-19 patients. Iwasakis laboratory is working to develop real-time analyses of immune markers and cytokines that could sharpen patient assessments and even inform treatmentdecisions.

The biggest surprise, so far, has been the role of interferon (IFN) in this disease, asserts Iwasaki. For other viruses, such as influenza and rhinovirus, type 1 IFN has a protective role for the host. But SARS-CoV-2 seems different. Studies in a mouse model have shown that IFN contributes to the inflammatory response without shutting down viral replication. According to Iwasaki, this is unusual. In other viral infections, IFN can shut down the virus. But Iwasaki thinks that the IFN here is being induced a little bit too late or in too small of an amount.

Iwasakis main goal is to understand what type of immune response confers protective immunity versus the types that lead to disease. Because patients have diverse responses to SARS-CoV-2, the researchers are working to build disease trajectories that reflect patient-specific aspects of the immune responsecytokine or antibody production, T-cell response, viral load, etc. By conducting longitudinal sampling and following patients trajectories, the researchers hope to predict how patients will fare when they are admitted to the hospital. Ideally, she envisions a panel that could be ordered by a physician that would allow patients to be treated with a more personalized medicine approach, based on their immune profiles.

This analysis has never been done so extensively for an infectious disease, Iwasaki asserts, because we never had the urgency to do this for other viral pathogens. In 2020, thankfully, the technology exists to do this type of analysis in real time.

Another area Iwasaki has recently explored is sex differences in SARS-CoV-2 infection. By studying male and female immune responses, her group found one clue as to why males are reportedly more susceptible to COVID-19. In a preprint posted in medRxiv, Iwasaki and colleagues described how they investigated sex differences in viral loads, antibody titers, and cytokines in COVID-19 patients, and how they found that T-cell activation was significantly more robust in women than in men. Men who dont develop a good T-cell response have worse disease outcomes.

Emma B. Hodcroft, PhD, a postdoctoral researcher at the University of Basel, recalls agreeing to keep her supervisors project going while he traveled. She was to take charge in early February. Continuity was important because they had just started uploading sequences of SARS-CoV-2 into the online genomics engine Nextstraina collaboration started in 2014 to track flu virus diversity and help predict the next flu strain.

Because Nextstrain has hubs in Europe and the United States, the absence of data uploads at the University of Basel would hamper runs during the European daytime. She has, in her own words, never looked back.

The pipeline analysis that Nextstrain runs makes phylogeny from viral genome mutations. Phylogenetics is a field full of limitations, Hodcroft notes. She adds that the field is particularly troublesome because its beautifully dangerousthe picture that is drawn is always less certain than it looks. While it is tempting to start telling stories about these sequences, she says, one must be cautious. The roughly 40,000 cases currently in the system is a drop in the bucket compared to the number of COVID-19 cases. There is much more likelihood that we havent sampled someone than we have, she admits.

As borders reopen and travel resumes, continued genomic analysis, Hodcroft tells GEN, could uncover details about virus transmission, including transmission routes. She will be keeping a close watch while cautiously communicating new findings. These data are of interest to a large and growing audience, and members of this audience may misinterpret (intentionally or not) what they hear. Deciphering the uncertainty that surrounds the field of phylogenetics requires expertisesomething not all scientists who have ventured into the world of COVID-19 phylogenetics possess.

Hodcroft gets upset when misinterpreted data spark a storyline that needs to be debunked. I dont think that telling these false stories that panic the public helps anybody, she declares. There is plenty to be worried about with this virus.

COVID-19 is the second SARS epidemic Rachel Graham, PhD, has worked on since she started her graduate work in a coronavirus lab in 2002. Currently working in a large coronavirus laboratory at University of North Carolina (UNC) led by Ralph S. Baric, PhD, she says that Barics group has scaled up from what was a busy program to an extremely busy program.

Graham uses large sequence sets to study how the virus transcriptional program contributes to replication and virulence. As the virus mutates, its subgenomic RNAs are produced in different ways, indicating that the transcription itself may be a virulence factor. She says that as the population acquires more herd immunity, researchers may see a lot of transcriptional differences in the virus, and these differences could result in changes in virulence. SARS-CoV-2 will be the first virus where this relatively new idea in virology will be examined in detail.

Lisa Gralinski, PhD, assistant professor of epidemiology at UNC, has been studying coronaviruses for 12 years. Her current work centers around virus host interactions, specifically in animal models such as the humanized ACE2 transgenic mouse. The mouse was developed at UNC in the mid-2000s after the first SARS outbreak. Researchers had even started the paperwork to cryopreserve the mouse just before COVID-19 struck. Quickly adjusting to COVID-19, they changed course and started as many breeding pairs as possible.

Graham and Gralinski may be new to the UNC faculty, but they are veterans in a rapidly growing field. Gralinski notes that six months ago, few people worked in coronavirus. Unlike SARS, SARS-CoV-2 is not currently a select agentwhich means that more people are free to work on it. Both Graham and Gralinski welcome more hands on deck, but theyve been alarmed by some of the ways that people are working with SARS-CoV-2 in their Biological Safety Level 3 (BSL3) labs. SARS-CoV-2 requires special precautions and security due to the high titers used in experiments.

In early March, Anne L. Wyllie, PhD, an associate research scientist in epidemiology at Yale, was chatting with her colleague, Nathan D. Grubaugh, PhD, an assistant professor of epidemiology. He was lamenting the level of SARS-CoV-2 RNA detection in patient samples. Wyllie drew his attention to a method she had been using to detect Streptococcus pneumoniae from saliva samples of asymptomatic carriers.

Her method, which used Thermo Fishers MagMAX Kit for Nucleic Acid Extraction, had worked so well for Wyllie that she suggested that Grubaugh use it to test for SARS-CoV-2. Wyllie recalls that when Grubaugh and colleagues compared the methods, Wyllies method blew the other one out of the water. Ultimately, the MagMAX Kit and the King Fisher platform (which happens to be named Frankie in the lab, in honor of Rosalind Franklin) became the Grubaugh laboratorys method of choice. Wyllie is now co-lead on the COVID-19 project with Grubaugh.

Wyllie was the lead author on a preprint uploaded to medRxiv showing that saliva samples offer a more sensitive and consistent alternative to nasopharyngeal swabs for COVID-19 testing. Saliva samples, the paper argued, should be considered a viable alternative to nasopharyngeal swabs to alleviate COVID-19 testing demands. This could be key to meeting public testing demands.

We knew a pandemic would come and we knew we would have to be ready, says Viviana Simon, MD, PhD, professor of microbiology at Mount Sinai School of Medicine. A decade after starting her virology laboratory in 2006, Simon and her colleagues built the Virology Initiative in 2017, which allowed real-time access to samples from patients with viral infections. The goal, she explains, was to study emerging viruses in New York Cityviruses such as Zika, chikungunya, and dengue. Having the initiative established allowed the laboratory to spring into action when the pandemic hit. Simon notes that a virology infrastructure capable of such responsiveness would not be easy to build in the middle of a pandemic.

Simon remarks that there was never any doubt that there would be a pandemic: We thought that it would be a respiratory virus and figured that it would be an avian influenza strain. Any pandemic would almost certainly come through New York City, which serves as a gateway not just for people, but for viruses from all over, she says.

Simon tells GEN that her team heard rumors about a new virus in December and began preparing. The moment the first sequences were released in mid-January, she recalls, We ordered primers. And then? Simon and colleagues waited and waited, she says, for the first case to show up. The first COVID-19 case was diagnosed at Mount Sinai on February 29. Only then could the Simon team grow the virus and sequence it.

Simons team has analyzed the genetic diversity of SARS-CoV-2 circulation in New York City and how the virus was introduced. The team is also interested in assessing the durability of antibodies and determining the degree to which antibodies are protective.

The size of Simons laboratory has doubled, primarily due to a temporary influx of postdoctoral researchers and technicians, volunteers that come from laboratories shut down by COVID-19. This COVID task force jumped in to support the COVID-19 research being done at Mount Sinai. Simon remarks that when temporary personnel start returning to their own laboratories, she will be busy hiring more people.

The dedicated researchers highlighted in this article have been working almost nonstop for months, motivated by a shared passion to beat back a virus that has taken over the world. These researchers represent different scientific backgrounds, and they are tackling different facets of the virus. But they would no doubt recognize common elements in their professional development. For example, the challenges that come with being women in male-dominated fields. Hopefully, it will not take decades to recognize and celebrate the contributions of some of these outstanding scientists.

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Tiny mineral particles are better vehicles for promising gene therapy – University of Wisconsin-Madison

Posted: July 8, 2020 at 3:58 am

University of WisconsinMadison researchers have developed a safer and more efficient way to deliver a promising new method for treating cancer and liver disorders and for vaccination including a COVID-19 vaccine from Moderna Therapeutics that has advanced to clinical trials with humans.

The technology relies on inserting into cells pieces of carefully designed messenger RNA (mRNA), a strip of genetic material that human cells typically transcribe from a persons DNA in order to make useful proteins and go about their business. Problems delivering mRNA safely and intact without running afoul of the immune system have held back mRNA-based therapy, but UWMadison researchers are making tiny balls of minerals that appear to do the trick in mice.

These microparticles have pores on their surface that are on the nanometer scale that allow them to pick up and carry molecules like proteins or messenger RNA, says William Murphy, a UWMadison professor of biomedical engineering and orthopedics. They mimic something commonly seen in archaeology, when we find intact protein or DNA on a bone sample or an eggshell from thousands of years ago. The mineral components helped to stabilize those molecules for all that time.

William Murphy

Murphy and UWMadison collaborators used the mineral-coated microparticles (MCMs) which are 5 to 10 micrometers in diameter, about the size of a human cell in a series of experiments to deliver mRNA to cells surrounding wounds in diabetic mice. Wounds healed faster in MCM-treated mice, and cells in related experiments showed much more efficient pickup of the mRNA molecules than other delivery methods.

The researchers described their findings today in the journal Science Advances.

In a healthy cell, DNA is transcribed into mRNA, and mRNA serves as the instructions the cells machinery uses to make proteins. A strip of mRNA created in a lab can be substituted into the process to tell a cell to make something new. If that something is a certain kind of antigen, a molecule that alerts the immune system to the presence of a potentially harmful virus, the mRNA has done the job of a vaccine.

The UWMadison researchers coded mRNA with instructions directing cell ribosomes to pump out a growth factor, a protein that prompts healing processes that are otherwise slow to unfold or nonexistent in the diabetic mice (and many severely diabetic people).

mRNA is short-lived in the body, though, so to deliver enough to cells typically means administering large and frequent doses in which the mRNA strands are carried by containers made of molecules called cationic polymers.

Oftentimes the cationic component is toxic. The more mRNA you deliver, the more therapeutic effect you get, but the more likely it is that youre going to see toxic effect, too. So, its a trade-off, Murphy says. What we found is when we deliver from the MCMs, we dont see that toxicity. And because MCM delivery protects the mRNA from degrading, you can get more mRNA where you want it while mitigating the toxic effects.

The new study also paired mRNA with an immune-system-inhibiting protein, to make sure the target cells didnt pick the mRNA out as a foreign object and destroy or eject it.

Successful mRNA delivery usually keeps a cell working on new instructions for about 24 hours, and the molecules they produce disperse throughout the body. Thats enough for vaccines and the antigens they produce. To keep lengthy processes like growing replacement tissue to heal skin or organs, the proteins or growth factors produced by the cells need to hang around for much longer.

What weve seen with the MCMs is, once the cells take up the mRNA and start making protein, that protein will bind right back within the MCM particle, Murphy says. Then it gets released over the course of weeks. Were basically taking something that would normally last maybe hours or even a day, and were making it last for a long time.

And because the MCMs are large enough that they dont enter the bloodstream and float away, they stay right where they are needed to keep releasing helpful therapy. In the mice, that therapeutic activity kept going for more than 20 days.

They are made of minerals similar to tooth enamel and bone, but designed to be reabsorbed by the body when theyre not useful anymore, says Murphy, whose work is supported by the Environmental Protection Agency, the National Institutes of Health and the National Science Foundation and a donation from UWMadison alums Michael and Mary Sue Shannon.

We can control their lifespan by adjusting the way theyre made, so they dissolve harmlessly when we want.

The technology behind the microparticles was patented with the help of the Wisconsin Alumni Research Foundation and is licensed to Dianomi Therapeutics, a company Murphy co-founded.

The researchers are now working on growing bone and cartilage and repairing spinal cord injuries with mRNA delivered by MCMs.

This research was supported by grants from the Environmental Protection Agency (S3.TAR grant 83573701), the National Institutes of Health (R01AR059916, R21EB019558, NIH 5 T32 GM008349) and the National Science Foundation (DMR 1105591, DGE-1256259).

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