i got low amount of rna for all my samples (less than 10ug), but got to save them for real time pcr and microarray. i heard it is important to do dnases treatment of sample before real time/conventional pcr to avoid genomic contamination, but after dnases treatment, the sample should be clean up which i think my rna will be lost some in this step. I design my primers span exon-exon junction, will that help to avoid genomic dna amplification if i don;t dnases my sample? thanks
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chrisbelle
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Posted 16 December 2009 - 12:47 AM
If you have exon-exon spanning primers then there's no need to do DNase treatment. 10ug? per uL or?
Chris
Chris
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wntiong
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Posted 20 December 2009 - 08:36 PM
chrisbelle, on Dec 16 2009, 04:47 PM, said:
If you have exon-exon spanning primers then there's no need to do DNase treatment. 10ug? per uL or?
Chris
Chris
1ug/ul. need 10 ug in 10 ul for microarray. due to sample scarcity, hard to get this amount for my samples.
