I once accidentally destroyed the agarose gel filling in my last sample, simply because i punctured the gel with the tip. Whats even funny is that i had a group of 5 others who were watching me as if their life depended on my hands.
you made two sets of wells in a single gel, how did you know that the fragments from the upper wells won't travel THROUGH and hit the second row of wells?
@1006Will You can monitor it by keeping track of the migration dyes. In the video, you will see there are two colored dyes. The fastest moving one runs at about 500 base pairs. So, if you know the sizes of your DNA, you can prevent it from running into the next set of wells.
This whole thing can be done in 1.5-2 hours. Depends on your conditions and number of samples.
I was wondering if you or anyone else here could explain to me why there is a need to identify sizes of DNA. What is the point of this exercise? Can you extract the DNA after it has been separated?
@ZScarabello There are lots of reasons to know the sizes. Verification of constructs, genotyping, cloning, etc. But the simple answer is, yes, you can extract the DNA from the gel if needed. I have done it several times.
@gkpeter One reason I perform gel electrophoresis to identify the size of the DNA band is to determine if the primers I used in PCR (Polymerase chain reaction - used to amplify small quantities of DNA into the thousands) actually cut the DNA to the length I needed. If you are only focusing on looking at a certain section of DNA primers will "cut" the section out you need, then they will be amplified to the thousands using PCR. You can then run the product out on a gel to determine if it cut
@ZScarabello actually not always the size is being determined. this is the way we can actually see if we have an insert (desired trait) in your DNA sample, and in this process we can cut the specific characteristic of your desired trait to put it in a transgenic species, it is important in Biotechnology, the result is called chimera. yes you can extract the DNA after separation..
@Peachpassion9 Compare it to a DNA ladder or molecular weight marker. You can guesstimate it or graph the known mass vs. length of migration from the well. You graph it on semi-log graph paper.
@Peachpassion9 I don't have a video for that yet, but plan on it. Maybe next week. You compare your band to the band on the marker. If they ran about the same length, then they should be about the same size.
@Peachpassion9 you dont actually calculate the size, it is indicated on the first marker. note that every DNA has its own characteristics. every marker has its own interpretation.. there are application on the net that actually calculate the relatiuonships of these markers.
A molecular weight marker (commonly known as the ladder) contains DNA strands with known sizes (in base pairs) and so allows you to determine the size of your samples by comparing them to that reference.
We are just learning about this in my AP Biology class, and this video helped me understand it a lot! Thanks! :)
eyeslikestars001 1 week ago
Great video, it helped me a lot during lab!
ronaldo204100 1 week ago
Damn i so glad i worked in a lab over the summer, otherwise i'd be screwed right about now
kyywii 2 weeks ago
I once accidentally destroyed the agarose gel filling in my last sample, simply because i punctured the gel with the tip. Whats even funny is that i had a group of 5 others who were watching me as if their life depended on my hands.
CiaoBello21 1 month ago
lol shaky hands
fappingfrenzy 1 month ago
thank you for this video
luar2521 2 months ago
This has been flagged as spam show
sorry for my question but what makes the fragments produce these lines?I mean how thin or thick they will be.
iwannaknoxville 2 months ago
Comment removed
iwannaknoxville 2 months ago
Looks like Smurf jizz.
Lupucillo 2 months ago
buffler @ 1:55
tranceaddictallnight 10 months ago
at school we didnt make the gels we just brought them ahead of time for the lab.
volleyball994pimp 1 year ago
thanks i am doing this for science fair and i was wondering how it works
iney1000 1 year ago
We did this in lab today; it can be VERY tedious.
AStrummerNamedJoe 1 year ago
Thank you for the video! I have to do this in college soon. It was nice finding an electrophoresis video not in spanish finally hah
fcdog555 1 year ago
Hi Questions:
you made two sets of wells in a single gel, how did you know that the fragments from the upper wells won't travel THROUGH and hit the second row of wells?
secondly, how long does the whole process take?
1006Will 1 year ago 2
@1006Will You can monitor it by keeping track of the migration dyes. In the video, you will see there are two colored dyes. The fastest moving one runs at about 500 base pairs. So, if you know the sizes of your DNA, you can prevent it from running into the next set of wells.
This whole thing can be done in 1.5-2 hours. Depends on your conditions and number of samples.
gkpeter 1 year ago 4
@gkpeter Hi, I was just wondering what DNA gel is used for? Is it used in skin care products?
BigBoss7777777 9 months ago
How are the wells numbered?
canaan1967 1 year ago
Hi gkpeter,
I was wondering if you or anyone else here could explain to me why there is a need to identify sizes of DNA. What is the point of this exercise? Can you extract the DNA after it has been separated?
ZScarabello 1 year ago
@ZScarabello There are lots of reasons to know the sizes. Verification of constructs, genotyping, cloning, etc. But the simple answer is, yes, you can extract the DNA from the gel if needed. I have done it several times.
gkpeter 1 year ago
@gkpeter One reason I perform gel electrophoresis to identify the size of the DNA band is to determine if the primers I used in PCR (Polymerase chain reaction - used to amplify small quantities of DNA into the thousands) actually cut the DNA to the length I needed. If you are only focusing on looking at a certain section of DNA primers will "cut" the section out you need, then they will be amplified to the thousands using PCR. You can then run the product out on a gel to determine if it cut
HawaiiZach 1 year ago
@ZScarabello actually not always the size is being determined. this is the way we can actually see if we have an insert (desired trait) in your DNA sample, and in this process we can cut the specific characteristic of your desired trait to put it in a transgenic species, it is important in Biotechnology, the result is called chimera. yes you can extract the DNA after separation..
phitox008 1 year ago
this is cool
ZOMIBErevolution 1 year ago
daaaaamn this is a community college??? we dont even have these high quality molecular replication equipment and im at a university :-/
foeasy16 1 year ago
thnx 2 upload, well plz explain the function of EtBr in electrophoresis, basically
noorchaudery 1 year ago
how do you calculate the size of DNA fragments in the cut DNA samples?
Peachpassion9 1 year ago
@Peachpassion9 Compare it to a DNA ladder or molecular weight marker. You can guesstimate it or graph the known mass vs. length of migration from the well. You graph it on semi-log graph paper.
gkpeter 1 year ago
Do you have a video that shows this?
Peachpassion9 1 year ago
I have the lambda HindIII genome, but I don't know how I calculate the size of the DNA fragments I compare it with.
Peachpassion9 1 year ago
@Peachpassion9 I don't have a video for that yet, but plan on it. Maybe next week. You compare your band to the band on the marker. If they ran about the same length, then they should be about the same size.
gkpeter 1 year ago
Comment removed
Peachpassion9 1 year ago
@gkpeter Well, thanks for the help. I appreciate it. :)
Peachpassion9 1 year ago
@Peachpassion9 you dont actually calculate the size, it is indicated on the first marker. note that every DNA has its own characteristics. every marker has its own interpretation.. there are application on the net that actually calculate the relatiuonships of these markers.
phitox008 1 year ago
perfect
jesca215 1 year ago
very good
5/5
gracias por subir este video van 5 estrellas
proteinP53 2 years ago
question. what is molecular weight marker? what does it do?
valkyriemissiles 2 years ago
A molecular weight marker (commonly known as the ladder) contains DNA strands with known sizes (in base pairs) and so allows you to determine the size of your samples by comparing them to that reference.
kayouna 2 years ago
Thank you.
deefromott 2 years ago
Great work there, were gonna do one next wednesday at school hope it will work!
andythrash 2 years ago
Comment removed
canaan1967 2 years ago
Wonderful
Good work .. thanx
0749061 2 years ago
it is handly for basic level of understanding about gel electrophoresis. thank you!!
amazaan 2 years ago
No problem, if you need anything else explained, feel free to ask.
gkpeter 2 years ago
can you talk a little about the results? or maybe type a few lines or something please??
cheers~
sukiwooty 2 years ago
very useful. thank you
bulletforthetrooper 2 years ago
No problem, if you need anything else explained, feel free to ask.
gkpeter 2 years ago