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Questions related from Melissa Yeow
I have whole genome data in fasta format, and the gene/protein sequences of the target enzymes. I've tried BLAST for 2 sequences, but the results are strange, possibly because the whole genome...
19 December 2018 1,368 2 View
I've been having trouble with purifying my DNA post-PCR using gel extraction techniques as I lose all my DNA and have a 230nm peak which may be contamination by ethanol of guanidinium salts. Any...
04 December 2018 8,566 0 View
I start with impure PCR products of >500ng/ul, 260/280=1, but peaks present at 260, and end up with peaks near 230, about 10ng/ul concentrations of 260/280=1.5 or so, which I assume is not DNA...
30 November 2018 6,899 8 View
According to protocols I found from Nature (Heckman et al 2007) and Cold Springs Harbour (Forloni et al 2018), the PCR products must be purified using gel electrophoresis and then a QIAquick gel...
06 November 2018 4,789 9 View
The identification of a protein differed based on RAST and protein BLAST results. Is RAST reliable? Or does this mean that both are correct and the protein has both identities? Eg it is a subunit...
17 September 2018 4,467 0 View