What happen to the longer products? Are they thrown away or kept in the mixtures? If they are thrown away, how to do that, and how you measure the final concentrate so that you are sure, that only the correct product remains?
@L30n3r1 If you were listening, after a certain amount of cycles, you'll have such a substantial copied amount of the "wanted" DNA fragment that to choose the wrong sample to work with would be highly improbable. Measuring the final concentration, is probably explained else where, but for sure, not here. Also, knowing what you want can be further analyzed using Protein Electrophoresis, but that's a whole different concept. ;)
Guys, taq polymerase is the most commonly used but not the only enzyme that works in a PCR, that is why they simply mention a generic "DNA polymerase". This video is very easy to follow and I think is pretty much correct. Thanks so much for the explanation!
O.K this makes sense to me for amplifying a piece of DNA but how does this process work for determine the amount of virus in a sample of blood? How can someone amplify the DNA and then determine the original amount? It doesn't make sense to me.
well actually the correct sequence ans the target sequence are the same...cause the target sequence is the one you wanna amplify...and the correct one is also the one you wanna amplify...it's just to show you that the long sequences aren't just what you're looking for!
i need this in french!
FRANÇAIS PEOPLE FROM CANADA!
torktt 1 month ago
sweet bass line
Benysaj13 1 month ago
great video! Now I understand :D
deepbit 1 month ago
and this is why youtube is awesome
willrap4f00d 1 month ago
wow and suddenly pcr makes sense
Number1JDAWG 2 months ago 2
I want it in PORTUGUESEEEEEEEEE! Some dedicated student could translate it!
Please!
AmeliaThermopolis007 2 months ago
very helpful, thanks
3385sandra 2 months ago
@darthawsome: you're right, I hate thinking too
grooshmonkey 3 months ago
Shouldn't the number of correct fragments be (N^2)-2N where N is the number of cycles? I think they frigged up on the 30 one, no?
grooshmonkey 4 months ago
@grooshmonkey Don't be a douche. It's just explaining the basic mechanics of PCR.
darthawsome 3 months ago
God bless you
moos209 4 months ago
I wish they didnt include the awful music in the video. It only distracts and serves no purpose. Thanks for posting. Very helpful despite the music.
salemr86 4 months ago
@salemr86 I like the music.
maplecrisp 2 months ago 4
too much bass
Robitybobitybobity 5 months ago
is it wrong if this video gave me a boner?
DkanDywoot 5 months ago
grt vdeo,keep it up.......
ridamughal98 6 months ago
haha i was watching this and was thinking "i'll post a wanking comment cause it's a chick teaching me to do science"... *scrolls down*...
I'm so proud of you guys!
zzaccc15 8 months ago 8
i found this difficult to masturbate to
fuzzb0y 9 months ago 10
@fuzzb0y #LOL
UlTrA2GaMeR 7 months ago
PCR always DTF!
nickd 10 months ago
Jizzed in my pants
R6ngas 1 year ago 2
Comment removed
poltergeistx 1 year ago
@poltergeistx
it is not right...you need nucleotides=Desxoxynucleosid-triphosphates(Nucleotid=Nucleosid+Phosphat)
as you know-the DNA cannot exist without phosphat!!!!!
h2so4hno31 9 months ago
@h2so4hno31 why in heavens did I say that 0_o I feel ashamed lol
poltergeistx 9 months ago
she sounds HOTT
thimwarrior 1 year ago 5
got d topic 4 dissertatn....can nebody help????
jinal896 1 year ago
Heating, hybridization, DNA synthesis. Hooray for me! Lol.
P3T3RYANG 1 year ago 2
youtube helps and your video does too
MaximumMaxime 1 year ago
What happen to the longer products? Are they thrown away or kept in the mixtures? If they are thrown away, how to do that, and how you measure the final concentrate so that you are sure, that only the correct product remains?
L30n3r1 1 year ago
@L30n3r1 I think the longer fragments are simply ignored, as they barely influence measurements.
Mattprole 1 year ago
@L30n3r1 If you were listening, after a certain amount of cycles, you'll have such a substantial copied amount of the "wanted" DNA fragment that to choose the wrong sample to work with would be highly improbable. Measuring the final concentration, is probably explained else where, but for sure, not here. Also, knowing what you want can be further analyzed using Protein Electrophoresis, but that's a whole different concept. ;)
P3T3RYANG 1 year ago
BEAUTIFUL
542eastWA 1 year ago
I love the beat what's it called and where can I get it?
Cali55nine 1 year ago
This has been flagged as spam show
what does she mean by "the primers are hybridised"? that RNA nukleotides are repleaced by DNA nukleotides?
SwedishPersian 1 year ago
Comment removed
SwedishPersian 1 year ago
Thanks so much for the upload. Things make much more sense now! :)
pinflipoy 1 year ago
brilliant. puaha.
YT092 1 year ago
ITS FANTASTIC.
nimeetgarg 1 year ago
k I would shove my dick up this girls fuckin clit
cohen36 1 year ago
@cohen36 I think you don't know what a clit is.
bench175 1 year ago
@cohen36 Hahaha, now that's gotta hurt.
Moonshield15 1 year ago
This video helped answer my questions about what happens to the original template and the "long" strands. Thanks.
miglspam 1 year ago
So is there like a formula?
(Typical exam question):
"How many correct copies of double stranded DNA containing only the target sequences are present at the end of the 35th PCR cycle?"
2^N (N = # of cycles) = total quantity DNA molecules present in mixture.
2N = # non-precise partially d/s DNA molecules.
So (2^N) - (2N) = # of ds DNA molecules precisely the length of the target sequence = # clones of the DNA sequence of interest.
Answer is then -> 3.44 * 10^10 copies.
Rock on bitches.
karlkarlkarl1234 1 year ago
@karlkarlkarl1234 haha u made the shit so easy, i thought i was gonna study my ass off for this crap
Alxphat 1 year ago
Excelent !
mrohith2010 1 year ago
Great Video, very concise and easy to understand. Thanks,
quasarinstruments 1 year ago
Whoever came up with PCR is freakin' brilliant!
josenros 1 year ago
@josenros
I will tell my dad that you complimented him.
Edensnator 7 months ago
Guys, taq polymerase is the most commonly used but not the only enzyme that works in a PCR, that is why they simply mention a generic "DNA polymerase". This video is very easy to follow and I think is pretty much correct. Thanks so much for the explanation!
flusete 1 year ago
if you want to amplify a specific gene, the primers are supposed to go on the outside of the target sequence.
sweetsweetdna 1 year ago
O.K this makes sense to me for amplifying a piece of DNA but how does this process work for determine the amount of virus in a sample of blood? How can someone amplify the DNA and then determine the original amount? It doesn't make sense to me.
ethanhines 1 year ago
theres no mention of taq polymerase here!!!!
DarkMetaRidley 1 year ago
@DarkMetaRidley yes thts true but she keeps on mentioning the dna polymerase, and i think only taq pol is actually used in pcr
SH3Z4D1 1 year ago
SVP di moi comment faire pour enregistrer ce video c urgent
merciiiii
amounaamounaalgrie 1 year ago
@amounaamounaalgrie :télécharger le plugin "Download Helper" pour Firefox
ethanhines 1 year ago
Nice, but the value after 30cycles is wrong it needs to be 2^30-1-29-29-1=1.073.741.764
Correct me if I am wrong
windowwatcher123 1 year ago
why read it when you can watch it? makes so much more sense! fuck!
elmatto2006 1 year ago 106
@elmatto2006
Hey this is science. you shouldn't use such language
Kiwibro92 1 year ago
@Kiwibro92 im mearly expressing my love for this video. it saved me in biology class.
elmatto2006 1 year ago
AWESOME.
I hava an exam tomorrow and this thing SAVED ME-
thank you so much garlandscience!!! :D
MissMetallica93 2 years ago
well actually the correct sequence ans the target sequence are the same...cause the target sequence is the one you wanna amplify...and the correct one is also the one you wanna amplify...it's just to show you that the long sequences aren't just what you're looking for!
lafleur21 2 years ago
great vid but i dont get it what do u mean by "correct sequence" and "Target sequence"? How do we know which is correct! HELP MEEE!!!
ismaelsbaby 2 years ago
Nt = 2 (n) x N0
mimiandolini 2 years ago
Little formula is necessary:
Number of DNA copies at n(th) cycle = 2 to the power n copies
mimiandolini 2 years ago
sexy
pablovox 2 years ago 39
Thank you very much
great work
donpadrementirosso 2 years ago
thanks
AlgerienBiologist 2 years ago 2