This tutorial helped me a lot with my home set up testing laboratory. Really fun.
@leafdaun4 жыл бұрын
Thanks.. I'm biomedical undergrade, quite years not practice pcr. Your vid, refresh the memories. Planning to volunteer for testing covid in lab. Tqvm again
@mr.nightt4 жыл бұрын
Me too... I am a PhD graduate who joined academia right after graduation, and spent 4 years in teaching and administration :( This video brings back the good memories of my PhD journey...
@walrus42484 жыл бұрын
I really appreciate that, hope you get to do that.
@rubenlanca92244 жыл бұрын
PCR is used to reproduce (amplify) selected sections of DNA or RNA for analysis
@khgnew7634 жыл бұрын
RNA can be amplified?
@beaa81534 жыл бұрын
cls new you have to create cdna molecule from it first
@khgnew7634 жыл бұрын
@@beaa8153 yes for that reverse transcriptase is needed
@rockymilano20713 жыл бұрын
If a cat were to walk through covid spit on sidewalk and then cat walks all over your outdoor property including vehicles,tables, benches etc. is it possible that a human could contract the virus? Please comment. Please
@SaraShahid11924 жыл бұрын
So thoroughly explained.. thanks for the amazing video..❤
@arresteddevelopment21584 жыл бұрын
Interesting. What I thought all along. Combined with Antibody testing, it should help greatly.
@zuay90164 жыл бұрын
Hi there, just to clarify, the viral RNA is detected during the reverse transcriptase PCR steps right? Then, the cDNA amplified at the end of the process is considered positive? What I mean here, you do not make cDNA library first right, then proceed with qPCR?
@pandora-id-netconsortium18464 жыл бұрын
Hi Ain, PCR cannot amplify RNA, so we must make cDNA first, using the viral RNA as our template. In this video, we show one step RT-PCR, where you create the cDNA using reverse transcriptase and then amplify it using polymerase in the same tube. There are also two step kits, where these steps are done separately. So yes, it is the cDNA that is considered positive, but you have to make it before you can amplify it.
@zuay90164 жыл бұрын
@@pandora-id-netconsortium1846 Thank you!
@khgnew7634 жыл бұрын
What is the sensitivity of this highly laborious procedure. In my country many false negative report is seen. Two different labs give two types report. Poor reliability. What are the pitfalls?
@pandora-id-netconsortium18464 жыл бұрын
The sensitivity of the test relies on many factors, for instance the extraction method, which kit you use and what gene your primers target. This is why it is vital to validate your testing procedure using standardised controls etc. PANDORA are creating a Global Health Network hub specifically to provide SARS-CoV-2 diagnostic test validation guidance. You may find that the two laboratories you speak of are doing entirely different protocols and if one is poorly validated compared to the other, they will have vastly different specificities and sensitivities.
@nataliebarratt74454 жыл бұрын
Fantastic informative video ! GREAT WORK
@jorges95244 жыл бұрын
Hi there, I have no medical background, but out of curiosity, what is the maximum number/range of patient samples that can be tested at once with a 96 well PCR machine?
@pandora-id-netconsortium18464 жыл бұрын
Hi Jorges, as a minimum, you would need to run a negative control (e.g. a water sample processed from the beginning with the real samples) to check for (cross)contamination and a positive control (e.g. confirmed SARS-CoV-2 nucleic acid) to ensure the results that you are seeing are the right thing. Often more controls are run for extra confidence, but in theory the maximum number of samples you could run on a 96 well PCR machine is 94.
@annazborowska37314 жыл бұрын
@@pandora-id-netconsortium1846 Hi, as each sample should be run in triplicate or at least in duplicate, the number of samples tested is reduced to 30 or 46 per 96-well plate.
@CHUBIBO1433 жыл бұрын
Is this a hard test to perform?
@PriyaSingh-js7nb4 жыл бұрын
thank you so much for this informative video..i was waiting for it
@octavstanculescu11004 жыл бұрын
Hi. Thanks for this i really appreciate the info. I have a question. Do you think it would be possible to use several swabs from different people in a single test? It would not tell you anything about every single person but it would help eliminate an entire community from testing if the global test is negative. Could this be done?
@pandora-id-netconsortium18464 жыл бұрын
Hi Octav, you make a really good point and you certainly can 'pool' lots of samples together to speed up testing. If your 'pool' then comes back positive, you will have one or more individual samples which has tested positive, which you can then test individually. This type of technique works best when you have a low incidence of a disease in a community, although it is a good way of identifying asymptomatic infections. At the moment, most countries have more cases than they can test, so are more likely to concentrate on diagnosing individuals (e.g. patients in hospital or front line staff).
@octavstanculescu11004 жыл бұрын
@@pandora-id-netconsortium1846 thank you for your answer. I am glad to see that this is a real possibility and I would think that trough this method you could diagnose not individuals but entire communities and quarantine them or at least raise the awareness that there is a a high risk and have people take precautions. With test so scarce these days, I would think this method could save lives. Once again thank you for your answer.
@SABkibaatvlog4 жыл бұрын
may i know what is your target sars-2 virus gene or protein?
@saibhadra69314 жыл бұрын
GENE IS RT PCR AND PROTEIN RAPID TEST
@vincevasquez58414 жыл бұрын
Yep, dont forget to amplify it correctly, if you dont, good luck finding out if you have a false positive, or a true positive which if you get it high enough, everyone can test positive. Once you find out what the origin is for what you are testing for, you will understand why.
@bang-naim4 жыл бұрын
Hello, thank you very much for the crystal clear video, very helpful :) Pardon me for my ignorance, I have something to ask.. I'm not sure why this protocol is not defined as real-time PCR, since the protocol demonstrated in the video also generated amplification/amplicon curve.. Would you please elaborate? Thank you very much!
@pandora-id-netconsortium18464 жыл бұрын
Hi Putra, you're correct, this is real time PCR. It is also known as quantitative PCR. The naming gets confusing, as this is reverse transcriptase (because you are turning RNA into DNA) real time PCR. So in actual fact its full name would be, RT-RT PCR, or RT-qPCR. This starts to get a bit long, so it is usually just called RT-PCR, or sometimes RT-qPCR.
@bang-naim4 жыл бұрын
@@pandora-id-netconsortium1846 Thank you very much for the reply :)
@jayagopalkrishna87904 жыл бұрын
@Monky Hi. I think ELISA is used to detect HIV
@kaustavphd4 жыл бұрын
@@jayagopalkrishna8790 confirmatory is RT PCR..or western
@khgnew7634 жыл бұрын
@Monky for HIV the Ab detection is more reliable. As the virus may not be found in blood for long time. Usually ELISA or western blot is sufficient
@md.bayejidhosen85844 жыл бұрын
Thank you very much for your informative video...
@Ezunglora4 жыл бұрын
Thank you esp. For the protocol..
@tridiep45033 жыл бұрын
Thanks for sharing this video
@jabedkhondaker38214 жыл бұрын
Thanks such an approach 🇧🇩
@geethuthomas48724 жыл бұрын
What disinfectant did you use for wiping the microcentrifuge ?
@thesciencewala3 жыл бұрын
if it is not quantitative type PCR for covid19 diagnostic, then which one is this . could you or anybody through light on this. As it is really confusing some says it is quantitative while others mentioning it as qualitative.
@MediaBuster4 жыл бұрын
How can they test for something UNTIL they show it is the causative agent? makes no sense.
@satyendrasrivastava88514 жыл бұрын
Why she didn't wear mask ...
@imeesurbakti61094 жыл бұрын
And what do you think about the use of rapid IgG and IgM for COVID19?
@pandora-id-netconsortium18464 жыл бұрын
Hi Imee, serology tests are also being developed currently. Serology tells us if a person has been exposed to the SAR-CoV-2 virus, but it cannot tell us whether it is a current infection or not, because it is looking for the person's immune reaction to the virus, which continues after the actual infection and virus has gone. Serology is good for identifying how many in population has contracted the virus during the outbreak, or whether a person (such as a doctor) has already had it (perhaps asymptomatically) and therefore would be able to continue working. In comparison, PCR tests that identify viral nucleic acid tell us whether a person has a current infection. So they have slightly different uses, but are both still very helpful in an emergency situation like this.
@khgnew7634 жыл бұрын
@@pandora-id-netconsortium1846 what are the possible ways that the virus can be spread in the laboratory
@kiethz82014 жыл бұрын
@@pandora-id-netconsortium1846 I have a challenge for you. Try testing things like say, apples, pineapples, oranges, water from the tap, watermelon, (raw chicken eggs those for sure) or anything else they use in flu vaccines Be sure whatever is used was fed GMO feed laced with Glyphosate/Round up. etc. Use a variety of things. Run those at 40 cycles and see what happens. If you can get your hands on any flu vaccines from last year late 2019 test them as well to see what is in them. Vasculitis is caused by a few vaccines. They found that to be a finding, in many of the Autopsy reports from Covid Patients that died. These vaccines are the one I am most interested in. Afluria, Engerix-B, Fluarix, Fluzone, Havrix, MMR-II, Recombivax, Twinrix
@DICKdeNORMATITY4 жыл бұрын
@@kiethz8201 you forgot mayonnaises!
@happymaker23444 жыл бұрын
good video. thank you.
@bigband97473 жыл бұрын
why not see step 72oC. taq polymerase DNA the best at 72oC. and take image at 72
@dharmendrashakya79904 жыл бұрын
Go for more videos...u r doing great job ..ur videos are awesome but channel is having less content
@hediehasani12564 жыл бұрын
Perfect video
@CallMeShoe4 жыл бұрын
Hey could you explain how Germany is able to do so much testing? Are they doing PCR testing and I’ve noticed they are pooling samples. Could you explain?
@ninjabrown85603 жыл бұрын
because they have a lot of pharmaceutical factories they already had the infrastructure in place to do mass testing - not quite sure if this is correct but hope it helps anyway lol
@johnnycongamusic4 жыл бұрын
Great video. Now what do we do with all the korean test kit videos that are bombarding the space?
@annarozycka-irzykowska51144 жыл бұрын
Good evning.. Very helfull video. I have a questions.. Can the results be interpreted differently depending on the person who interprets them? Is it possible for one person to describe the same sample as positive and the other to be negative? Is there a limit above which all samples are considered positive?
@pandora-id-netconsortium18464 жыл бұрын
Hi Anna, these are good questions! The good thing about real time PCR is that it does provide you with a visual representation of the data at the end. Once a procedure has been validated, and as long as you use positive and negative controls, identifying positive and negative results is fairly straight forward (i.e. does the curve for a particular sample have the same shape as the positive control and does is rise above the negative control lines (which should be flat?) Some RT-PCR programmes will automatically provide results if you set it up to. Results can be subjective though, if you have a very small viral load to begin with, it will take much longer for the line to rise above the background level (or 'reach the cycle threshold'). Laboratories typically set a CT value cut off (usually around 35 cycles), so that any sample with a CT value of higher than that is considered a negative (background fluorescence can start to amplify after a lot of cycles). So whilst RT-PCR machines (and good validation of a specific test) mean that it is usually fairly simple to tell positive from negative. It is not always the case. Depending on the test you set up, RT-PCR machines can be semi quantitative or quantitative. Whilst diagnostics and clinical trials are governed by strict quality control, often more research based science (and depending on the tests used) can be very much opinion based. I hope you found this useful, please don't let negative comments like the one below put you off!
@linzyelton45924 жыл бұрын
@@beamarie8041 There's no need for comments like this
@beamarie80414 жыл бұрын
@@linzyelton4592 Yea you're right so I took it down. There have just been so so many unbelievably rude conspiracy comments on this video and countless others that I started getting frustrated and pissed off thinking this was another one. Sincere apologies to OP, I misread the comment and the rudeness was for the conspiracists lol.
@beaa81534 жыл бұрын
Maria Taylor what you wrote? I agree there is many conspiracy theorist on testing. They are small so it is ok. (I am learning english apologies)
@Cotelarouche4 жыл бұрын
Maria Taylor the question is fair but I see how you can mistake it -> getting angry and responding to conspiracy comments is useless - they are annoying, but harmless...
@anshulpathak34604 жыл бұрын
Very nice
@mayankrana89434 жыл бұрын
Procedure should not be done without wearing n95 mask and the PPE Kit, PPE is must for handling the deadly virus.
@khgnew7634 жыл бұрын
How this virus can spread in the laboratory?
@pandora-id-netconsortium18464 жыл бұрын
Hi Mayank, this was filmed in a UK BSL3 laboratory. The health and safety requirements in the UK mean that there is a strong negative pressure gradient moving away from the user and out through a HEPA filter in the microbiological safety cabinet (MSC). As you can see, all work in the video is being conducted within the MSC and therefore laboratory workers are not exposed to aerosols etc. unless there is a spill outside the cabinet (there are emergency procedures in place for this). So there is no need to wear a face mask, because you are protected by negative air pressure. The BSL rules differ depending on your country and also the level of laboratory (currently, according to the WHO, SARS-CoV-2 samples can be processed in a BSL2 laboratory within an MSC, but any culturing must be at BSL3 level). It may well be necessary to wear face PPE in many laboratories if the health and safety standards are different (we work with many countries setting up BSL3 laboratories and the standards vary hugely). This is is something you must check before undertaking any pathogen work.
@khgnew7634 жыл бұрын
@@pandora-id-netconsortium1846 if we use bsl2 safety cabinet for extraction we don't need face masks?
@houcinechoubane95794 жыл бұрын
Thank you
@joshnelsonnj4 жыл бұрын
Is this process automated usually or are samples run as shown in the video?
@pandora-id-netconsortium18464 жыл бұрын
Hi Joshua, this is likely to depend on the laboratory processing the samples. There are automated extraction and PCR preparation machines available, but it would depend on the size and income of the laboratory. As this video is aimed providing information to Low and Middle Income countries, such as those in the PANDORA-ID-NET consortium, we wanted to show all of the individual, manual steps.
@joshnelsonnj4 жыл бұрын
@@pandora-id-netconsortium1846 thanks for your reply. I was a lab researcher for several years, now a high school biology teacher and was curious about how samples are processed and how throughput has changed. Thanks again.
@hoverboverer3 жыл бұрын
@@joshnelsonnj Hello Joshua. I've been working in a testing lab for the last year, We still handle some samples manually, but most are lysed in deep (96) well plates using robotic liquid handlers which also add magnetic beads and phage (extraction control). Extraction (via the beads) is automated as is mastermix prep and prep of PCR plates. We do approx 40-60K a day between 150-200 lab techs.
@olidelao27554 жыл бұрын
Hi, great video! I have a question, is there a difference between thermal cyclers for conventional PCR and RT-PCR, does a RT-PCR needs a specific type of thermal cycler?
@annarozycka-irzykowska51144 жыл бұрын
No its the same
@khgnew7634 жыл бұрын
@Nenad Ilić what is the role of the probe? Is it tagged with fluorescent matterial?
@jsslime57904 жыл бұрын
Thought mullis the inventor stated this shouldn't be used to diagnose infectious disease ? Am I missing something here ?
@anthonygaydotcom4 жыл бұрын
Exactly. Scamdemic it is.
@thatbossguy1234 жыл бұрын
wouldn't you do end point PCR?
@evelynvillanueva66454 жыл бұрын
Thank you!
@hoagybob4 жыл бұрын
Why not put the microfuge in the hood? Keep it simple.
@itsame22714 жыл бұрын
shouldn't RT stand for Reverse Transcription ??
@Rajesh-ij4ty4 жыл бұрын
Thanku make for this video
@alexioforte3974 жыл бұрын
How accurate is this test?
@alexioforte3974 жыл бұрын
There testing symptoms? Who let this happen!
@alexioforte3974 жыл бұрын
@@fabriciooliveira3720 so I could litterally have any infections or viruses and I'll have a good chance of testing a false positive?
@pandora-id-netconsortium18464 жыл бұрын
RT-qPCR is very sensitive, as in theory you only need one strand of DNA for the primers to pick up and amplify. There are a number of different protocols which are used and adapted by different countries, all of which vary slightly, but they will have all been validated to ensure that they are suitably specific and sensitive for SARS-CoV-2. They will have positive controls and negative controls, potentially including controls against human DNA, ensuring that it is only viral RNA that is being picked up by the primers. The primers have been designed to be specific for the sequence in SARS-CoV-2 genes (scientists search for sequences in a massive database to ensure that they are unique), so will only pick up this virus' nucleic acid pattern. This means that it will only pick up SARS-CoV-2 and not any other virus.
@pandora-id-netconsortium18464 жыл бұрын
@@fabriciooliveira3720 Perhaps it would be useful for you to provide your reference for this comment, so that it can be justified?
@waddie964 жыл бұрын
@@pandora-id-netconsortium1846 The issue isn't necessarily the sensitivity of your test (and primers in this case, which is debatable), but the quality of our specimens, when I have time I'll post some of articles the here, but the general consensus from a few articles is a 30-71% sensitivity of our current RT-PCR if we collect NP-throat swabs (even early in the disease when VL is relatively high in that site)
@richardprice97304 жыл бұрын
A long time since I was a burgeoning Marine biologist, became disillusioned with Japanese texts books full of details on ameba when all I want to do was study telepathy with dolphins, but wonderful to see Dr Mullius' pioneering work put to good use the sophistication and automation of the test he originally cobbled together is amazing, bless him what is his book dancing naked in the rain like , he would be stimulating company, reading Tarthang Tulku at the moment similarly inclined God bless R
@abhibhadran26474 жыл бұрын
If we know, we extracted the viral RNA, then what's the point of doing PCR of that ?
@SpillFreakMusic4 жыл бұрын
Abhi Bhadran duhhh boy! We are extracting any random RNA from human swab and identifying covid 19 rna through the covid 19 probe
@mash76414 жыл бұрын
How long does it take ?
@pandora-id-netconsortium18464 жыл бұрын
Hi Maha, do you mean the whole process? This depends on how many samples your are processing at a time, and also whether the process is automated at any stage. If you are doing it all by hand, as in the video, the RNA extraction is likely to take around 1 hour (plus then quantification of the nucleic acid), then the PCR stage (setting up the reaction and running samples on the machine is likely to take another 4 hours
@Tonytango4 жыл бұрын
My understanding is the actual COViD-19 was never isolated. If this is true. What RNA nucleotide is being replicated??
@aparkostavicenna10624 жыл бұрын
Maybe exosome
@kdcruz754 жыл бұрын
Shhhhh....dont let the cat out of the bag
@cjdabes4 жыл бұрын
Before proceeding, I think it's important we get the terminology correct: COVID-19 is the disease, SARS-CoV-2 is the etiological agent (i.e. the virus). So you would isolate SARS-CoV-2, not COVID-19. Virions of SARS-CoV-2 have been isolated, the RNA extracted and amplified, the subsequently sequenced across many samples. You can check the publicly available NCBI website, where the sequences of thousands of samples from throughout the world have been submitted and can be downloaded (as FASTA files, a type of .txt file). For fun, you can take these files and put them into a phylogeny program (there is free software for this) to form a parsimonious tree to approximate the phylogenetic relationship of existing sequenced samples. Sequencing technology is quite rapid compared to what it was only a 2 or 3 decades ago. For example, in a small project investigating some novel bacteriophages (viruses that infect bacteria) that I was involved in had 2 of our phages sequenced and data retrieved in under 2 weeks. The sizes of those 2 phage genomes were 50 kilobases (kb) and 150 kb long, both of which are significantly larger than that of SARS-CoV-2 (only ~30 kb).
@beamarie80414 жыл бұрын
Hákon Sigurðarson THANK YOU...But they won’t understand. They don’t want to understand.
@beamarie80414 жыл бұрын
Nenad Ilić and the earth is flat because no human while on earth can see it as round. Astronauts are paid actors, alex jones said so!
@imeesurbakti61094 жыл бұрын
hi there, how about the use of genexpert? do we still need dna sequencing after that? tq
@pandora-id-netconsortium18464 жыл бұрын
Hi Imee, Cepheid got emergency approval for a SARS-CoV-2 cartridge for the GeneXpert very recently. As this is classed as an 'emergency' roll out, the sensitivity and specificity of the test will likely need to be validated. The GeneXpert does utilise PCR, so it works in a similar way. Cepheid have some good videos on KZbin about how it works.
@oguzhanbali51404 жыл бұрын
Hi ,What is the risk of transmission of disease test employees?
@pandora-id-netconsortium18464 жыл бұрын
Hi Oğuzhan, The risk to laboratory staff is very low, as long as they follow their local health and safety protocols whilst processing these samples. SARS-CoV-2 has been designated a hazard group 3 pathogen, so the extraction of viral RNA must be done in a BSL3 laboratory within a microbiological safety cabinet to protect workers from aerosols (who must also wearing the appropriate personal protective equipment). Once the RNA is extracted, no live viruses will be present (as they are broken open to extract the nucleic acid), so the resulting samples can then be moved to a BSL2 laboratory for the rest of the protocol (quantifying and PCR). The RNA extraction part of this protocol should only be undertaken by laboratory staff who are trained to work in a BSL3 laboratory.
@big_bad14 жыл бұрын
Pct should not be used for diagnostic purposes it's a know fact
@priscywilliam57244 жыл бұрын
Why so. It's the most accurate one as we target the genes directly
@esaimorales8144 жыл бұрын
Craig Doe Because it says so in the insert. It is an amplification technique not a diagnostic one. The inventor himself said as much but he’s no longer alive as of a few months ago to refute its use as he did when it was being used for hiv testing and ‘viral load’ counting. He wrote a paper titled ‘Viral Load Of Crap’ as a matter of fact. Dr Kary Mullis. A great scientist and principled human being. Look him up.
@DynamexxTV4 жыл бұрын
@@esaimorales814 I totally agree!! Makes no sense, even using this for the Pandemic. its crazy stats going on because of this. Do you have that Paper he wrote, or you have a link?
@txemaraxx93144 жыл бұрын
Alguien lo puede traducir todo al español o decirme un resumen no muy largo de que va? Es que tengo un trabajo sobre este vídeo y no me entero de na en inglés. Gracias saludos
@gregoire594 жыл бұрын
hay un enlace en la descripción del video al articulo publicado. ella sigue el protocolo
@pandora-id-netconsortium18464 жыл бұрын
Estamos trabajando en una versión en español, sigue revisando nuestro canal de KZbin
@txemaraxx93144 жыл бұрын
Gregoire Riviere gracias ya lo vi 👌🏽
@txemaraxx93144 жыл бұрын
PANDORA-ID-NET Consortium gracias por la aportación , pude traducirlo perfectamente 👌🏽
@smrutiisweta89544 жыл бұрын
Ma'am I have a question, is there any medicine like nasal wax or nasal spray that could resist the virus to get anchored to the nasal cells for 24 hours?
@pandora-id-netconsortium18464 жыл бұрын
To our knowledge, there is so far no evidence that nasal wax or nasal spray would prevent or treat COVID-19. In any case, any treatment should be tested in a controlled environment, i.e. as clinical trials and published in respected peer viewed journals before being delivered or used by the community. Viruses can be spread through mucous membranes including the mouth, so you would need to protect all potential entries into the body.
@sundarkumarakella64064 жыл бұрын
I am not a biology student, just curious, can't we just see the virus under strong microscopes?
@pandora-id-netconsortium18464 жыл бұрын
Hi Sundar, whilst SARS-CoV-2 is quite a large virus, viruses in general are too small to see with a conventional light microscope. You can see them using electron microscopy, but unfortunately this isn't practical for large-scale diagnosis (they are expensive and take up huge amounts of space).
@rain-gb5nx4 жыл бұрын
noo
@shehbaz2054 жыл бұрын
Hi Linzy Elton, this is very good and informative. Kindly also make a video about HCV RAN diagnosing PCR
@youssefjerrari61573 жыл бұрын
nice,
@evat.suarez10554 жыл бұрын
RT-PCR does not stand for Real Time PCR, it stands for Reverse Transcription PCR..... pretty reliable video
@jazz1ba4 жыл бұрын
She said real time RT PCR
@khgnew7634 жыл бұрын
What is the difference between real time PCR with reverse transcriptase PCR
@baghiballsakh824 жыл бұрын
🤣 As stated she said 'real time RT PCR' That's to say *real time reverse transcription polymerase chain reaction* Oh dear 🤦🏻♂️ You really wouldn't know a reliable video would you 🤷🏻♂️
@hammadmufti40074 жыл бұрын
@@khgnew763 It's not really a question of difference. RT- PCR stands for Reverse Transcriptase- PCR. We call it that because we use reverse transcriptase enzyme to make a complimentary DNA from the viral RNA. This is necessary because we cannot amplify an RNA alone in a PCR. Amplified DNA tells us indirectly that the sample is positive for viral RNA that means the patient is positive for the virus, i.e., coronavirus in this case. As far as the word 'Real-time' is considered, we call this Real Time PCR because on the screen you can see the progress of the Polymerase reaction in real time and the detected viral load increases (the line on the graph rises) as time passes if Coronavirus was present in the sample. Hope this settles it.
@khgnew7634 жыл бұрын
@@hammadmufti4007 greatly explained
@khgnew7634 жыл бұрын
is the virus still remain infectious after extraction of RNA?
@vincevasquez58414 жыл бұрын
Nope. It never was/is infectious. The way they proved polio caused paralysis was by continuous applications on many animals with no evidence. It was until they drilled monkeys in the head and Injected a cup and a half of virus filled water. One died, the other was paralyzed, then died. If this is the science people are IGNORING, I can see why...
@khgnew7634 жыл бұрын
@@vincevasquez5841 but after polio vaccine this paralysis has been reduced dramatically
@ibrahimnabi70564 жыл бұрын
Hi, in our country (Algeria) we just have a few labs with qPCR (fluorescence), not sufficient in terms of processed samples per day ; the question is : could we establish the diagnosis Covid-19 on classic PCR (gel electrophoresis) by yielding samples as templates of cDNA and positive control cDNA?
@pandora-id-netconsortium18464 жыл бұрын
Hi Ibrahim, RT-qPCR is preferred as a diagnostic tool, because the results are more sensitive and specific. However, where RT-qPCR is not widely available, conventional PCR could be used as a pragmatic tool, as long as appropriate validation of the assay has been undertaken. Different countries have different rules as to what diagnostic tests are acceptable, so you should check if classical PCR is approved for diagnostics in Algeria.
@ahmedlabidi67954 жыл бұрын
Hey dude, im from algeria as well. Is it true that only Pasteur's institution got a qPCR?
@bajaboy274 жыл бұрын
So gloves not required?
@av.fahriyeecekaradag58784 жыл бұрын
so according to your pcr results, samples are positive for covid 19, right?
@buongiorno72694 жыл бұрын
Yes it is
@dawnmorille99754 жыл бұрын
Cuz these test kits are not supposed to be used for diagnostic proposes but for research.
@beamarie80414 жыл бұрын
RT-qPCR can result positive or negative depending if a cDNA fragment of interest is present or not. If there was no viral RNA, then there would be no template for cDNA, and despite thermocycling, it would result negative. Like the negative control shown in the video.
@D34DH34D4LYF3 жыл бұрын
safety glasses are your freind
@ebrukaradag55394 жыл бұрын
Thank you 👍 all of this have to pdf? If been to please send a mail for me? Thanks
@اسامةمحمدطاهر-ض4ط2 жыл бұрын
Hi iam dr osama can you send me prosedure step by step
@pandora-id-netconsortium18462 жыл бұрын
Hi Dr Osama, you will find all the accompanying information on our TGHN pages: pandora.tghn.org/covid-19-diagnostic-tools/molecular-diagnostics/ and a link directly to the protocol from the video here: media.tghn.org/medialibrary/2022/02/Outbreak_diagnostics_SARS-CoV-2_-_Protocol.pdf
@mozg3d4 жыл бұрын
hey yo) you have viruses) can you please test the following vaccination procedure: take blood, separate leukocytes, add viruses, wait, inject back into patient. In a week antibodies should be in blood) thanks
@gooner4lyf4 жыл бұрын
Artem Rodichkin wait, what?😳🤦🏼♂️🤦🏼♂️🤦🏼♂️🤦🏼♂️
@hammadmufti40074 жыл бұрын
There are cheaper available methods for comiting homicide.
@akshayavasarkar4 жыл бұрын
Hi. How does MS2 as an internal control performs against Rnase p Internal control in a one tube multiplexing reaction for Sars cov ( s, n and orf1ab)
@roberttharp96364 жыл бұрын
Why is she not wearing a mask if it so deadly?
@eridon55774 жыл бұрын
Mask is not needed. She's using a biosafety cabinet(negative air pressure + HEPA) google to see how they work. Airflow is pull away from her
@pandora-id-netconsortium18464 жыл бұрын
@Nenad Ilić You're correct, there are two types of cabinet, a class I (which primarily protects the user) and a class II (which protects both the user and the sample. As Eri said, in the UK, for BSL3 laboratories, we use negative pressure systems, which drag airflow away from the user and out through the top of the microbiological safety cabinet through a HEPA filter. So the user is never exposed to aerosols if work is done within the cabinet. Because of this, in the UK, masks are not required. However, these health and safety rules can vary a lot between countries and some do require masks (because they rely less on negative pressure, which can be expensive to set up). Ebola is a BSL4 pathogen and requires even greater health and safety requirements. The current WHO guidelines state that SARS-CoV-2 samples can be processed in a BSL2 laboratory within a cabinet, but culturing of the virus must be at BSL3. Hope that helps