i sonicated my samples (Control,treatment). From there i had taken 100 ul samples and diluted with 400 ul of IP dilution buffer. from there i have taken 50ul as input and stored. from the remaining 450ul, 200 ul was aliquoted for Chip negative beads and chIP samples with specific antibody. I eluted my samples in 20ul elution buffer. after that i isolated genomic dna from chip samples and stored input and dissolved DNA in 50ul water. i quantified samples and concentration was 200ul for input, 35ul for beads only ,60ul for specific antibody. i took 1 ul of each and did qpcr. can anyone please tell about the dilution factor i should consider ? i am little confused about how to go about the percentage of input? can anyone please help me in calculating these data?

More Ishmat Ara Yasmin's questions See All
Similar questions and discussions