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Questions related from Molly Resnick
DNA was amplified using a PCR mix that included SYBR green dye. Could this DNA amplification undergo pyro sequencing without interference from the dye?
02 February 2016 2,669 5 View
We are having a perplexing issue with some IDT double-quenched probes. We have a particular amplicon with a SNP and have control DNA that is wild-type, heterozygous, and homozygous for the SNP....
01 January 2016 7,081 3 View
I am trying to use qPCR to genotype single nucleotide polymorphisms (SNP). Some of the SNPs are located in GC poor regions and I cannot get a probe Tm 8-10 degrees higher than my primer Tm. Do you...
06 June 2015 2,934 5 View
I am currently designing a SNP genotyping assay for CYP2D6 and I am confused about the alternate loci that keep appearing in my blast searches. What is an alternate locus? Does every gene have an...
03 March 2015 1,829 3 View
Hi, I am trying to find homozygous mutant DNA for CYP2D6*6. SNPedia, ARUP, and the literature says this SNP is a T deletion at nucleotide number 1707 (according to M33388 sequence). When I go onto...
01 January 2015 1,469 1 View
I sequenced with both the forward and reverse primers in separate reactions (one tube forward primer + amplified DNA, and the other tube reverse primer + amplified DNA). The reverse reaction shows...
12 December 2014 2,912 1 View
PCR was run with SYBR Green Taq and three different template DNAs that are wild type, heterogeneous, and homolozygous for a SNP. The only difference between the tubes is the template DNA. The...
12 December 2014 9,020 2 View