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#applications of pcr
healthcaremresearch · 2 years
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tiktaalic · 8 months
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I hope these questions don't annoy you, but whats it like working in a lab?
I'm considering the same career path cause I really like my lab classes so far
Not annoying! from what ive seen there are 3 or so types of labs, which are labs in the hospital, which are obviously a faster pace (did half of my preceptorship in one), reference labs, which get a fairly high volume since they're doing testing everybody's sending out for (did other half of my preceptorship in one), and privately owned labs which pick up samples from clinics urgent cares nursing homes etc (both of my jobs have been with private labs).
I like it! It's very routine. I have my set of tasks i do when i clock in and my set of tasks i do at the end of the night and in between I'm just sticking samples on the machines and releasing results. and there is imo enough variation to it to keep it interesting - troubleshooting failed qc, or double checking criticals, or having to do manual difs. if you're liking undergrad lab work I'm assuming you're doing stuff like pcr and gels and micro plates? which is a lot of what molecular departments do in a lab besides micro which is micro. I currently work in the core portion of a lab, which is hematology, coagulation, urinalysis, and chemistry. You really only break out the microscope for urinalysis and hem. we have a micro department that handles all the cultures, and a molecular department that does molecular testing. lots of labs have small micro factions and do lots of micro send out instead. the last lab i worked at did that. the hospital i did my preceptorship at would do plating, but then send all the plates out to be read and send out all the blood culture tubes to be cultured elsewhere. the lab I'm currently at does most cultures in house.
re: education to work in a lab you have to be ASCP certified. After I got my biology degree, I enrolled in texas tech's CLS certification program, which was 3 semesters of classes (preceptorships were the majority of the coursework the last semester). I didn't mind doing it because I was a fresh graduate and I didn't want to Career Hunt or go to grad school. so 3 sems to get a guaranteed job sounded great to me. Since I had my bio degree, I had most of the baseline credits out of the way. chem biochem ochem cell bio genetics etc etc. And the 3 sems I did were lab specific courses like blood banking, clinical chemistry, molecular methods, immunology, phlebotomy, lab management, clinical micro and hematology. there are tons of post bachelor's cls programs, and tons of them are delivered online so that you can chip away at it part time while working.
A nice thing about it is that you can get work literally anywhere. I moved to a town with a population of 90k. Applied for 3 jobs as a brand new graduate. and got 3 offer letters. the payscale's pretty variable, depending on where you are, but it is nice to know that i'm certified in like. 47 states and could get some sort of job in any of them no problem. i think once you've been certified a year you can get cali state certification, which is the route a lot of people go since cali is on the high end of the pay scale. it'll depend on what the lab you're at is like, obviously, but it is pretty difficult to get day shift positions since what a lot of places do is open internal applications for any night/evening shift people who want to move up. I work an evening shift of 2pm to 11pm and i really like it. A very common complaint i see is that there's no like... career ladder. if you're a bench tech. you're a bench tech. which sometimes gets parlayed into section leader, or section manager, but that's a years of experience thing.
My plan is to work in the same place for a couple of years so I feel more experienced, and then to take a few travel contracts which are shorter term higher pay. again, they're available pretty much anywhere, but sometimes the tradeoff is lower compensation or a worse shift or being in the middle of nowhere america. but i think it'll be fun to get paid to bop around the country for awhile. I like my job and I like that it's very secure, but I do plan to go back to school for Something Else at some point and probably shift careers. My review: good thing to do in your twenties! good thing to have under your belt in general. very dependable.
if you have other questions in general or about anything I said you can 100% msg me! Ik I had a lot of trouble finding info when I was looking into this as an undergrad
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skelayton-lord · 2 months
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@angelofthemornings Making this a proper reply-post because as a reply it might end up being too big.
The field is very vast, but the most common would be the person that runs the tests a physician asks you to and signs the paper to validate the results - we can be found doing your bloodwork, urine, biochem analysis (which all falls under clinical analysis/clinical pathology), and many other fields like radiology (x-rays, tomography, etc), acupuncture, embryology... here in Brazil we can have up to 29 licenses, each one corresponding to a different field. Some of these you can come out of university ready to work due to experience in your internship, but some others will require a specialization course or a master's - like acupuncture and radiology.
My license is in clinical pathology, but I've also spent a year in a specialization/expertise program (after getting my bachelor's degree) in laboratorial surveillance for diseases of public health interest, with a focus on diagnostic tools of immunology (serology tests) and molecular biology (mostly real time Polymerase Chair Reaction - PCR).
So I'm both licensed to work in any hospital or particular lab to run tests (with the objective of a diagnosis), and to work with the government in public health surveillance (where the objective here isn't a diagnosis, it is to confirm cases of a disease in a certain population and keep an eye out on how it behaves throughout the year, epidemiology).
I was about to decide between a Master's or a "direct" Doctorate (a Doctorate that "skips" a Master's and lasts longer than the usual Doctorate program) but then the pandemic came and many internship deals crashed, unless you were in virology, as that became the main and only focus of research at the time. I tried for a spot in the State's Strategic Lab, but it was interview-only and for only 1 candidate - I was placed 4th.
With that, my grandma's health also began to deteriorate, so I've been staying home since then to help care for her.
But 4 years later, I've started to job hunt again, and I'm now afraid I might be overqualified (and thus, "more expensive") to employers, as so far I havent gotten any return from my applications. I quite miss and wish to return to academia, sometimes, and with the State's lab, but I have a love-hate relationship with academia and it takes them forever to open up sign-ins for employees. Working in public health was my best time though, really, so if the opportunity arises, I'll be trying my chance there again - I did leave in good terms, and a lot o the chief researchers there wanted to work with me.
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rexaleph · 5 months
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is insight real or have i just almost made myself cry by thinking a new emotionally loaded thought abt myself for no reason and could have spent my energy better elsewhere. what is the practical application to having a story abt where a disturbing emotion comes from if the narrative focus makes the emotion worse.
am i digging at shit bc i started to identify w being mentally ill and want to make myself worse
is it the maybe-covid (negative pcr on sat, negative antigen yesterday) making me cranky again.
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renee-mariposa · 4 months
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Nothing in my day-to-day job shows me the limits of modern medicine like vancomycin does. And it makes me insane.
(extremely long, somewhat incoherent nerd rant below the cut)
See, vanc is really good at, like, three things: treating MRSA (when given IV), treating ampicillin-resistant enterococcus (when given IV), and treating c diff (when administered orally ONLY). Most every use outside of that, like when it’s used to treat methicillin-susceptible staph aureus for “penicillin allergic patients” (don’t get me started on PCN allergies), actually has data that it increases risk of morbidity and mortality (i.e. harm and DEATH).
Unfortunately, due to the prevalence of multi-drug resistant organisms, vancomycin is empiric therapy for a lot of presumed infections. And it's a lot more difficult to actually tell if someone has an infection than you'd think. A lot of medical conditions imitate each other and when time is of the essence to identify what's going on, the most ethical thing is to start an antibiotic and rule out infection as the hospitalization continues. Lab techniques have gotten a lot quicker: I can remember 8 years ago, it would take 3 days just to identify what microbe the patient had in their presumed infection. These days, anno domini 2023, PCR comes back in a matter of hours, identifying gram positive/gram negative staph/strep/bacilli/etc, and it's the sensitivities that take 2-3 days. (Don't get me started on contaminated cultures.) But even with improvements in lab technique, we might not culture any microbe at all or the provider might keep vancomycin on "just in case" because we don't know IF the patient is infected, WHAT they're infected with, or if the infection will get better with a different drug.
And vancomycin is terrible on kidneys. Extremely nephrotoxic. It isn’t as bad as the 80s when the drug first came out and was called Mississippi Mud colloquially, but it will fuck the patient up if not monitored closely.
But finding the correct dose for each patient in a timely manner is nigh impossible. This is because vancomycin is renally eliminated. We have to mathematically estimate how well the kidneys are working. Unfortunately, our mathematic equation is next to useless if you are:
-Less than 50 kg
-Shorter than 5 foot tall
-Have a BMI of more than 40
-Are an adult younger than 45 (twenty-year-olds get astronomical doses that would be destructive in an older patient)
-Are older than 65 (the official definition of 'geriatric', i'm relatively sure)
-Are female (this is really only applicable if the patient is less than 50 kg or older than 65 - think: little old frail lady - we have absolutely no fucking idea how their kidneys are doing until we order the serum drug level. It is next to impossible to accurately dose vancomycin in little old ladies on the first try.)
-Are missing limbs (lots of leg amputations in the older and impoverished diabetic population!!)
-Have a lot of muscle mass (think bodybuilder or really tall guys)
Fun fact: we estimate renal function by looking at height, weight, age, birth gender (few, if any, studies on trans patients taking HRT), and a lab value called serum creatinine. Creatinine is a byproduct of muscle metabolism, I don't know the fine details, but we can generally estimate how well kidneys are working by seeing how much creatinine is in the blood: low creatinine usually means kidneys are excreting it as they 'should' be. High creatinine means there's something wrong, the kidneys aren't able to excrete it as efficiently as they 'should' be. But the effect of low muscle mass and high muscle mass haven't been studied enough to be able to adjust our mathematical equation to compensate for them. And with high BMI: we often overestimate their renal function because we don't know how to estimate their muscle mass vs their body fat.
(I work out in the boonies. ~70% of our patients have diabetes. ~80% of our patients have a BMI of greater than 35. So what I'm trying to say here is: we are shooting in the fucking dark when we're estimating the renal function of the vast majority of our patients.)
Complicating this: vancomycin is useless until it reaches steady-state concentration in therapeutic range. On one side of this problem: a lot, if not most, medical providers assume that vancomycin starts working its magic from the first dose. So we sometimes get orders for "vancomycin 1 gram now and see how the patient is doing in the morning". That isn't going to solve jack shit! That's just going to increase the incidence of microbial resistance!!
OR, like in the multiple situations I dealt with this afternoon, you make an educated guess on what regimen is going to work for the patient. You get a level 48 hours after the dose starts. And you find out that you fucking guessed wrong and the patient is subtherapeutic. It has been two fucking days and the patient hasn't started being treated for their (presumed) infection yet!! And we've increased the possibility of microbial resistance! *muffled screaming in frustration*
So what I'm trying to say here is: on almost every presumed infection that comes into the hospital (which we're guessing like 30%? 50%? of the time), we're starting an extremely toxic drug, oftentimes 100% guessing what regimen will be therapeutic, only finding out in 2 days that it is not therapeutic, and it can sometimes take days and days to titrate the dose sufficiently to find a therapeutic regimen. And sometimes we're really fucking unlucky and we destroy the patient's kidneys temporarily (or permanently! but kidneys can be very resilient so that's thankfully rare) because we guessed a regimen that's too high!! This is a fucking nightmare!!!!!!!!
And if all of this wasn't bad enough, we don't really have any drugs that do what vancomycin does therapeutically. We have things that can be used to cover some of what vancomycin does, but nothing that's equivalent AND less toxic.
Like, to fix this situation, we need:
-Better education to providers on what drugs are appropriate empiric therapy for different presumed infections (we're working on it, we are working on it)
-Better ways to estimate kidney function (there needs to be more research on kidney function in patients with BMI greater than 35!! And little old ladies!! And patients with low body weight and high body weight and amputations and...)
-Better prognostic tools to tell 1. when the patient is infected (looking at you, sepsis!!!) 2. what they're infected with
-Less-toxic antibiotics AND/OR better ways to treat infection (this would be the evolution of medicine as we know it)
And I want to be clear: vancomycin isn't bad. It's an extremely effective tool when used correctly but we often either don't have enough data to use it correctly or the provider doesn't understand that this tool is fucking useless for the job they're trying to perform.
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studychemistrytopics · 3 months
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Bio-friendly transparent temperature sensor technology that precisely measures temperature changes by light
Researchers have developed a transparent temperature sensor capable of precisely and quickly measuring temperature changes caused by light. This technology is expected to contribute to the advancement of various applied bio devices that rely on sensitive temperature changes.
The photothermal effect using plasmonic nanomaterials has recently been widely proposed in various bio-application fields, such as brain nerve stimulation, drug delivery, cancer treatment, and ultra-high-speed PCR due to its unique heating properties using light. However, measuring temperature changes by photothermal phenomena still relies on an indirect and slow measurement method using a thermal imaging camera, leading to the limitation that it is not suitable for local temperature measurement at the level of a single cell, which changes rapidly at the level of several milliseconds to tens of micrometers.
Due to the absence of precise information on temperature changes, photothermal effect technology has raised concerns about the understanding of biological changes and stable clinical application resulting from precise temperature changes, despite the spreading effect of its application.
Read more.
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krill-joy · 1 year
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Medical Masks Versus N95 Respirators for Preventing COVID-19 Among Health Care Workers
Abstract
Background: It is uncertain if medical masks offer similar protection against COVID-19 compared with N95 respirators.
Objective: To determine whether medical masks are noninferior to N95 respirators to prevent COVID-19 in health care workers providing routine care.
Design: Multicenter, randomized, noninferiority trial. (ClinicalTrials.gov: NCT04296643).
Setting: 29 health care facilities in Canada, Israel, Pakistan, and Egypt from 4 May 2020 to 29 March 2022.
Participants: 1009 health care workers who provided direct care to patients with suspected or confirmed COVID-19.
Intervention: Use of medical masks versus fit-tested N95 respirators for 10 weeks, plus universal masking, which was the policy implemented at each site.
Measurements: The primary outcome was confirmed COVID-19 on reverse transcriptase polymerase chain reaction (RT-PCR) test.
Results: In the intention-to-treat analysis, RT-PCR–confirmed COVID-19 occurred in 52 of 497 (10.46%) participants in the medical mask group versus 47 of 507 (9.27%) in the N95 respirator group (hazard ratio [HR], 1.14 [95% CI, 0.77 to 1.69]). An unplanned subgroup analysis by country found that in the medical mask group versus the N95 respirator group RT-PCR–confirmed COVID-19 occurred in 8 of 131 (6.11%) versus 3 of 135 (2.22%) in Canada (HR, 2.83 [CI, 0.75 to 10.72]), 6 of 17 (35.29%) versus 4 of 17 (23.53%) in Israel (HR, 1.54 [CI, 0.43 to 5.49]), 3 of 92 (3.26%) versus 2 of 94 (2.13%) in Pakistan (HR, 1.50 [CI, 0.25 to 8.98]), and 35 of 257 (13.62%) versus 38 of 261 (14.56%) in Egypt (HR, 0.95 [CI, 0.60 to 1.50]). There were 47 (10.8%) adverse events related to the intervention reported in the medical mask group and 59 (13.6%) in the N95 respirator group.
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Limitation: Potential acquisition of SARS-CoV-2 through household and community exposure, heterogeneity between countries, uncertainty in the estimates of effect, differences in self-reported adherence, differences in baseline antibodies, and between-country differences in circulating variants and vaccination.
Conclusion: Among health care workers who provided routine care to patients with COVID-19, the overall estimates rule out a doubling in hazard of RT-PCR–confirmed COVID-19 for medical masks when compared with HRs of RT-PCR–confirmed COVID-19 for N95 respirators. The subgroup results varied by country, and the overall estimates may not be applicable to individual countries because of treatment effect heterogeneity.
Primary Funding Source: Canadian Institutes of Health Research, World Health Organization, and Juravinski Research Institute.
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industryinsights · 2 years
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Epigenetics Market Competitive Landscape, Growth Factors, Revenue Analysis Till 2027
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Epigenetics refers to the analysis and study of heritable changes in the gene function. It does not involve the study of changes in the DNA sequence like in a chromosome, phenotypic affecting the gene activity, or expression. Sources of these heritable changes could be external such as environmental factors, as well as biological factors such as age or disease. Some examples of Epigenetics are histone modification, which refers to the alteration of genes expressions without altering the DNA sequence, and DNA methylation.
The global Epigenetics Market is estimated to record a staggering CAGR of 12.9% during the forecast period. The primary factor responsible for the ascension of the global epigenetics market is the increasing prevalence of cancer. According to the statistics revealed by the World Health Organization, cancer was responsible for around 8.8 million deaths in 2015, indicating nearly 1 in 6 patients. Further, as per the Centers for Disease Control and Prevention, approximately 1.5 million people are diagnosed with cancer every year, in the US alone.
Other factors upscaling the global epigenetics market include the development of selective and highly sensitive tests, a concurrent rise in the computational power, along with instrumentation. Advancements such as the development of DNA and RNA modifying enzymes have provided the global epigenetics market with tremendous traction through the forecast period. Further, rising government support for biotechnology and growing partnerships between the academia and the industry are pushing the global epigenetics market exponentially. Other technological developments driving the global epigenetics market include the advances in PCR technology, automation of many processes, and the strategic and cross-functional nature of molecular diagnostic technology.
Market Segmentation
The global epigenetics market is segmented by consumables, instruments, applications, end-users, technology, and region. By instruments, the epigenetics market is segmented into spectrometer, PCR, NGS, and software solutions. Based on consumables, the epigenetics market comprises kit, reagent, and enzymes. By application, the epigenetics market is segmented into developmental epigenetics drug discovery biology, cardiology, oncology, and immunology. Based on technology, the global epigenetics market is segmented into histone modification and methylation. Based on end-users, the global epigenetics market is segmented into pharmaceutical, academia and research, and biotechnology industry.
Key Players
Bio-Rad (US), Illumina (US), QIAGEN (Netherlands), Thermo Fisher (US), Active Motif (US), Diagenode (Belgium), Agilent (US), Merck Millipore (US), Abcam (UK), New England Biolabs (US), PerkinElmer (US), Zymo Research (US) are some of the most notable players in the global epigenetics market.
Detailed Regional Analysis
The global epigenetics market is regionally segmented into North America, Europe, Asia Pacific, and the Middle East & Africa. Among these segments, North America held the largest share in the epigenetics market in 2016. Within North America, the U.S. is estimated to be at the forefront of the market by the end of the forecast period. This market domination can be owed to the fast-paced development of technology and the presence of the gigantic biotech industry in the country. Further, a greater presence of many market giants for epigenetics is propelling the epigenetics market, specifically the molecular diagnostics industry in the region.
Europe is anticipated to capture the second-largest market share for epigenetics through the review period. Germany, France, and the U.K. are expected to spearhead the country-specific epigenetics market. Europe is also projected to expand at the second fastest rate, with Asia Pacific showcasing a surge in the epigenetics market at the fastest rate. China, South Korea, Japan, and India are likely to lead the country-specific epigenetics market in Asia Pacific.
Alternatively, the Middle East & Africa are projected to augment at a moderate rate during the conjectured period. Such growth can be attributed to the impoverished industry landscape and lower demand for epigenetics owing to weak economic conditions.
Industry Update
May 2019: Juvenescence recently announced the creation of a new biotech company to target the epigenetic investigation of neurodegeneration. Souvien Therapeutics is the said new company launched by Juvenescence, a private investment firm that focuses on increasing healthy human longevity.
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reportsdata · 2 years
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DNA Polymerase Market Revenue, Growth Factors, Trends, Key Companies, Forecast To 2030
Reports and Data's Global DNA Polymerase Market research report is an in-depth investigation that provides an industry-wide overview of existing and emerging growth patterns, end-user analysis, and other key data that has been tested and validated by industry experts and professionals. The report examines the market in terms of importance, share, size, demand and supply, patterns, competitive landscape, industrial chain analysis, and other important factors. The report also provides a detailed outlook for the industry's driving and restraining forces, as well as micro and macroeconomic factors that are expected to influence its development. include Sigma-Aldrich Solutions, Thermo Fisher Scientific Inc., Bio-Rad Laboratories, Inc., Yeasen Biotechnology (Shanghai) Co., Ltd., GENAXXON bioscience, Promega Corporation, Cytiva Lifesciences, SBS Genetech Co., Ltd., BDI Biotech, and GenTegra LLC. In December 2021, SBS Genetech Co., Ltd. announced decrease in price of their mutant Proteinase K at USD 40/g. Mutant Proteinase K is one of the best-selling products of SBS Genetech Co., Ltd.,
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The DNA Polymerase market investigation report assesses the global market for the DNA Polymerase industry and provides revenue and capability forecasts for the projected period of 2022-2030. The factors that drive the industry's growth are highlighted in the report. The report divides the DNA Polymerase market into main categories such as forms, applications, end-users, technology, and others for a better understanding. These segments are thoroughly examined in order to provide a more accurate outlook for the global and regional markets. The report also examines the industry's major players, including their product portfolios, company overviews, strategic growth strategies, revenue generation, market share and market size, geographic presence, and development and manufacturing capabilities.
Market Overview:
Consumers are placing a higher importance on sustainability and, as a result, are choosing items based on factors like circularity and carbon footprint. Furthermore, consumer concern about carbon emissions has prompted increased investment in renewable energy, energy efficiency, and transportation decarbonization. These developments have had considerable impact on chemical end sectors, particularly in the automobile and construction industries. COVID-19 has exacerbated the situation by lowering the automobile and construction industries (as well as many others) and disrupting current supply lines.
The adoption of digital technologies by oil, gas, and chemical firms has been fueled primarily by cost savings and greater reliability. Many organizations in these areas saw excellent benefits from advanced market sensing, improved operational optimization, and expanded usage of "in silico" simulations. Companies' existing digital technologies provided an advantage with the abrupt entrance of COVID-19 and the accompanying shutdown of facilities and work sites, but they were often insufficient for the level of remote working and cybersecurity that was suddenly required.
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Origin Outlook (Revenue, USD Million; 2019-2030)
Prokaryotic DNA Polymerase
Eukaryotic DNA Polymerase
End-Use Outlook (Revenue, USD Million; 2019-2030)
Pharmaceutical Industry
Biotechnological Industry
Research Laboratories
Hospitals and Diagnostic Centers
Others
Application Outlook (Revenue, USD Million; 2019-2030)
DNA Replication
PCR
DNA Sequencing
Others
 The report is written with the aid of industry analysts, market segmentation, and data collection in order to assist readers in making profitable business decisions. The report includes a comprehensive database of technical and product advances. It also provides information on growth rates and market value, as well as a thorough examination of niche market segments. The report provides strategic advice to newcomers and existing businesses about how to make profitable and well-informed business decisions.
The DNA Polymerase market has been segmented into key regions of the world and offers an analysis of growth rate, market share, current and emerging trends, production and consumption ratio, industrial chain analysis, demand and supply, import and export, revenue contribution, and presence of key players in each region. A country-wise analysis of the market is offered in the report to gain a better understanding of the regional spread and progress of the DNA Polymerase market.
The global DNA Polymerase market is segmented into:
North America (U.S.A., Canada, Mexico)
Europe (Italy, U.K., Germany, France, Rest of Europe)
Asia Pacific (China, India, Japan, South Korea, Australia, Rest of APAC)
Latin America (Chile, Brazil, Argentina, Peru, Rest of Latin America)
Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of MEA)
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Key Questions Addressed in the Report:
What are the dominating factors that are influencing the growth of the industry?
In the forecast period, which market segment is expected to rise the most?
What are the risks and challenges that the industry is facing?
In the coming years, which area is projected to dominate the market?
Who are the major players in the market? What kind of strategic business plans have they made?
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Single Cell Analysis Market 2022 by Manufacturers, Regions, Type and Application, Forecast to 2030
Global Single Cell Analysis Market size was at US$ 3.1 Billion in 2021, and it is predicted that it will reach a valuation of US$ 10.99 Billion by the end of 2030 with an annual development rate (CAGR) of 15.10% between 2022 and 2030.
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Single-cell analysis has been used to learn more about how cellular functionality is implemented. It necessitates an understanding of many biological components such as protein composition, DNA, and RNA, as well as metabolites such as pigments. A single-cell analysis approach is a method for interpreting cellular and functional variations in a single cell.
Due to new emerging approaches in which genomic technologies are applied at the single cell level rather than to all cells collectively, Single Cell Genomics is a rapidly growing business. By distinguishing the contributions of single cells to the diversity of ecosystems and species, single cell genomic technologies are breaking new ground. Single cell genomics is also revealing new information about a variety of biological systems, ranging from microbial ecosystem diversity to human cancer genetics.
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The business models, major strategies, and respective market shares of some of the most notable players in this sector are all examined in depth in this Single Cell Analysis System market study. The comprehensive analysis includes market statistics in terms of revenues, segment-wise data, region-wise data, and country-wise data, as well as an in-depth commentary on the key affecting variables. This report is one of the most comprehensive documents available, covering every aspect of the growing Single Cell Analysis System market.
Global Single Cell Analysis Market: Segmentations
Single Cell Analysis Market based on product type
• Consumable
o Microplates
o Beads
o Reagents
o assay kits (Immunoassays and cell based assays)
o Other Consumables
• Instrument
o flow cytometers
o NGS Systems
o PCR Instruments
o Spectrophotometers
o Microscopes
o cell counters
o HCS systems
o Microarrays
o Others
Single Cell Analysis Market based on Cell Type
• Human cells
• Animal Cells
• Microbial Cells
Single Cell Analysis Market based on workflow
• Single cell isolation & library preparation
• Downstream analysis
• Data analysis
Single cell analysis market based on Technique
• Flow Cytometry
• Next-generation sequencing
• Polymerase Chain Reaction
• Microscopy
• Mass Spectrometry
• Others
Single Cell Analysis Market based on Application
• Research Application
o Cancer
o Immunology
o Neurology
o stem cell
o Others
• Medical Applications
o Non-invasive prenatal diagnosis
o in Vitro Fertilization
o circulating tumor cell detection
Single Cell Analysis Market based on End-User
• Academic & Research Laboratories
• Biotechnology & Pharmaceutical Companies
• Hospitals & Diagnostic Laboratories
• Cell Banks & IVF Centers
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rnomics · 9 hours
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Cells, Vol. 13, Pages 703: Establishment and Characterization of SV40 T-Antigen Immortalized Porcine Muscle Satellite Cell
Muscle satellite cells (MuSCs) are crucial for muscle development and regeneration. The primary pig MuSCs (pMuSCs) is an ideal in vitro cell model for studying the pig’s muscle development and differentiation. However, the long-term in vitro culture of pMuSCs results in the gradual loss of their stemness, thereby limiting their application. To address this conundrum and maintain the normal function of pMuSCs during in vitro passaging, we generated an immortalized pMuSCs (SV40 T-pMuSCs) by stably expressing SV40 T-antigen (SV40 T) using a lentiviral-based vector system. The SV40 T-pMuSCs can be stably sub-cultured for over 40 generations in vitro. An evaluation of SV40 T-pMuSCs was conducted through immunofluorescence staining, quantitative real-time PCR, EdU assay, and SA-β-gal activity. Their proliferation capacity was similar to that of primary pMuSCs at passage 1, and while their differentiation potential was slightly decreased. Si#RNA-mediated interference of SV40 T-antigen expression restored the differentiation capability of SV40 T-pMuSCs. Taken together, our results provide a valuable tool for studying pig skeletal muscle development and differentiation. https://www.mdpi.com/2073-4409/13/8/703?utm_source=dlvr.it&utm_medium=tumblr
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Autoimmune Disease Testing Market Future Scope Demands and Projected Growths to 2031
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The global autoimmune disease testing market has been on a steady rise, fueled by advancements in diagnostic technologies and the increasing prevalence of autoimmune disorders worldwide. According to recent market research, the market size was valued at USD 10.2 billion in 2022 and is projected to reach around USD 22.18 billion by 2030, exhibiting a remarkable compound annual growth rate (CAGR) of 10.2% during the forecast period from 2023 to 2030. This substantial growth is attributed to several key factors driving the expansion of the autoimmune disease testing market.
Emerging Trends and Opportunities
Technological Advancements: The integration of advanced technologies such as next-generation sequencing (NGS), multiplex assays, and biomarker discovery platforms has revolutionized autoimmune disease testing, enabling more accurate and comprehensive diagnostic solutions.
Rising Incidence of Autoimmune Disorders: The escalating prevalence of autoimmune diseases, including rheumatoid arthritis, multiple sclerosis, and lupus, among others, has significantly increased the demand for diagnostic testing, thereby propelling market growth.
Growing Awareness and Screening Initiatives: Increasing awareness about autoimmune diseases and the importance of early diagnosis, coupled with government initiatives and awareness campaigns, has led to a surge in screening programs, creating lucrative opportunities for market players.
Expanding Geriatric Population: With the aging population worldwide, there is a higher susceptibility to autoimmune disorders, driving the demand for diagnostic tests targeted at this demographic segment.
Focus on Personalized Medicine: The shift towards personalized medicine and precision diagnostics is driving the development of novel testing methods tailored to individual patient profiles, fostering market expansion.
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Key Drivers Propelling Growth
Advancements in Diagnostic Technologies: Continuous innovations in diagnostic technologies, such as immunoassays, polymerase chain reaction (PCR), and molecular diagnostics, have enhanced the sensitivity, specificity, and speed of autoimmune disease testing, driving market growth.
Increasing Healthcare Expenditure: The rising healthcare expenditure, especially in developed economies, coupled with favorable reimbursement policies for diagnostic tests, is boosting market growth by facilitating patient access to testing services.
Strategic Collaborations and Partnerships: Market players are increasingly entering into strategic collaborations and partnerships to expand their product portfolios, enhance R&D capabilities, and strengthen their market presence, driving overall market growth.
Focus on Early Diagnosis and Treatment: Growing emphasis on early diagnosis and intervention to improve patient outcomes and reduce healthcare costs is driving the adoption of autoimmune disease testing, thereby fueling market growth.
Expanding Applications in Research and Drug Development: Autoimmune disease testing is not only used for clinical diagnostics but also plays a crucial role in research and drug development, contributing to market expansion.
Challenges and Considerations
Regulatory Challenges: Stringent regulatory requirements and the need for extensive validation of diagnostic tests pose challenges for market players, especially smaller companies and startups, in navigating the regulatory landscape.
High Cost of Advanced Diagnostic Tests: The high cost associated with advanced autoimmune disease testing methods may limit their accessibility, particularly in emerging economies with limited healthcare infrastructure and resources.
Limited Awareness in Developing Regions: Limited awareness about autoimmune diseases and diagnostic testing options in developing regions may hinder market growth in these areas, necessitating targeted educational initiatives.
Technological Limitations: Despite advancements, certain technological limitations such as assay variability, cross-reactivity, and assay interference may impact the accuracy and reliability of autoimmune disease testing, requiring ongoing research and development efforts.
Key Takeaways from the Market
Market Expansion: The autoimmune disease testing market is poised for significant expansion, driven by technological advancements, rising disease prevalence, and increasing healthcare expenditure.
Opportunities in Personalized Medicine: There is a growing opportunity for personalized medicine approaches in autoimmune disease testing, emphasizing the need for tailored diagnostic solutions based on individual patient characteristics.
Collaborative Efforts: Strategic collaborations and partnerships will play a crucial role in driving innovation, expanding product offerings, and addressing key challenges in the autoimmune disease testing market.
Focus on Accessibility and Affordability: Addressing barriers to accessibility and affordability, particularly in underserved regions, will be essential for achieving equitable access to autoimmune disease testing and improving patient outcomes globally.
Continuous Innovation: Continuous innovation in diagnostic technologies and a focus on improving test accuracy, reliability, and affordability will be instrumental in shaping the future landscape of the autoimmune disease testing market.
In conclusion, the autoimmune disease testing market is witnessing robust growth driven by technological advancements, increasing disease prevalence, and evolving healthcare dynamics. While challenges such as regulatory hurdles and cost constraints exist, the market presents significant opportunities for innovation, collaboration, and expansion, ultimately leading to improved diagnosis, treatment, and management of autoimmune disorders.
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123567-9qaaq9 · 2 days
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DNA and RNA Sample Preparation Market Future Trends to Look Out | Bis Research
DNA and RNA sample preparation is a crucial step in molecular biology research, diagnostics, and various biotechnological applications. Proper sample preparation ensures the integrity, purity, and stability of nucleic acids, which are essential for downstream analyses such as PCR, sequencing, and gene expression studies. 
The global nucleic acid sample preparation market is projected to reach $5,615.9 million by 2033 from $2,922.8 million in 2023, growing at a CAGR of 6.75% during the forecast period 2023-2033.
DNA and RNA Sample Preparation Overview
Understanding of the key principles and methods involved in preparing DNA and RNA samples for analysis Importance of Sample Preparation, Sample Collection, Extraction of nucleic acid, quality assessment, DNA preparation, RNA preparation, quality control storage prevention 
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Key Market Players 
 Agilent Technologies, Inc.
 Autogen, Inc.
 Bio-Rad Laboratories, Inc.
Roche AG
Merck KGaA
and many others  
The Nucleic Acid Isolation and Purification Market has made an impact in the following ways:
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Market Segmentation
Product Type 
End Users 
Applications 
Geography 
Various different applications involved are as follows 
Polymerase chain reaction 
Sequencing 
Gene Expression 
Molecular Diagnostics
Epigenetics and Chromatin Analysis
Drug Discovery and Development  
 Market Drivers for DNA and RNA Sample Preparation Market 
Advancements in Genomic Research
Rising Demand for Molecular Diagnostics
Increasing Applications in Drug Discovery and Development
Rising Incidence of Infectious Diseases and Genetic Disorders
Demand for Point-of-Care Testing (POCT) Solutions
Recent Developments in the Nucleic Acid Sample Preparation Market
Qiagen N.V. introduced two groundbreaking additions to its sample technologies portfolio, i.e., the TissueLyser III that facilitates high-throughput disruption of diverse biological samples and the RNeasy PowerMax Soil Pro Kit that isolates high-purity RNA from challenging soil samples using advanced Inhibitor Removal Technology. Qiagen announced the launch of the QIAseq Normalizer Kits that give researchers a fast, convenient, and cost-effective method to pool different DNA libraries for best-quality results from next-generation sequencing (NGS) runs.
PerkinElmer introduced the CHEF Magnetic Bead Cleanup System, providing automated nucleic acid purification through advanced magnetic bead technology. This novel system would help automate the nucleic acid purification process efficiently. PerkinElmer (Revvity, Inc.) rebranded its diagnostics and life sciences business as Revvity. This strategic move marked a new identity and focus for the company's ventures in these sectors.
Conclusion
As the demand for accurate, reliable, and efficient DNA and RNA sample preparation continues to rise, there is a growing emphasis on developing automated, integrated, and cost-effective solutions to meet the evolving needs of researchers, clinicians, and diagnostic laboratories. The convergence of cutting-edge technologies, strategic partnerships, and market expansion efforts is expected to drive the DNA and RNA sample preparation market forward, facilitating advancements in genomic medicine, precision diagnostics, and therapeutic development. Overall, the future of the DNA and RNA sample preparation market appears promising, with ample opportunities for innovation, growth, and impact across various sectors of the life sciences industry.
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