DNA migrate differently in agarose vs PAGE gel
Posted 15 August 2011 - 08:46 PM
i am currently working a gene in leukemia. The mutant allele has been sequenced to contain 527 base pair. when i run an agarose gel to confirm, it did appear in the position approximately equal to 527 base pair according to the DNA ladder. HOWEVER, when i run a PAGE, it shows up at a different poistion!!(it is at about 600 base pair in PAGE!!!!). Yet the conditions were the same when i run the PAGE and agarose gel (150v, 30 mins)
I just wonder why this thing will happen and is it possible to happen.
Thx for your help!!
Posted 15 August 2011 - 08:59 PM
According to Fermentas troubleshooting, here is a list of things that may affect migration of DNA in gel:
Atypical migration due to different DNA sequence or structure. During high resolution electrophoresis DNA fragments of equal size can migrate differently due to differences
in DNA sequences. AT rich DNA may migrate slower than an equivalent size GC rich DNA fragment. DNA structures such as nicked, supercoiled or dimeric molecules will always show different mobility on gels compared to an equivalent DNA size standard.
Gel shift effect. The presence of DNA binding proteins in the sample, such as ligases, phosphatases or restriction enzymes may alter DNA migration in the gel or cause the DNA to remain in the gel wells. High salt concentration in the sample may also cause gel shift effects.
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Posted 15 August 2011 - 09:04 PM
..."best of our knowledge, as far as we know this had never been reported before, though I can't possible read all the published journals on earth, but by perform thorough search in google, the keywords did not match any documents"...
"what doesn't kill you, makes you stronger"---Goddess Casandra reminds me to be strong
"It's all just DNA. Do it."---phage434
Posted 15 August 2011 - 11:28 PM
But actually i am dealing with the same gene migrate differently in different gels instaed of different gene of the same size miigrate differently in different gels. So, would u think the difference in base pairs observed in different gel of the same gene be possible?