![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
H4K20me1 antibody in plants? | ewheeler | Epigenetics | 0 | 06-05-2016 03:50 PM |
Struggling to amplify DNA with barcoded primers | firefly2280 | Sample Prep / Library Generation | 4 | 09-30-2013 12:48 PM |
TruSeq DNA - need index/barcode-specific primers | drops | Illumina/Solexa | 5 | 12-05-2012 01:24 PM |
Mixture of antibody - ChIP-seq | huo | Sample Prep / Library Generation | 1 | 03-16-2011 03:03 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: NYC Join Date: Apr 2016
Posts: 6
|
![]()
I am setting up ChiP seq in the lab and am trying to use a widely popular antibody for chip - ab8580 histone antibody to standardize every step. After I crosslink and sonicate samples using covaris, I immunoprecipitate. Following ChIP i want to run a qPCR to test for antibody enrichment. I have sequence for the primers used from the company for active (GAPDH, PRPL30) and inactive genes (MYO-D, AFM), but these sequences are for human samples and my samples are mouse. how should i align these sequences for my samples ?
Thank you |
![]() |
![]() |
![]() |
Thread Tools | |
|
|