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Questions related from Arvind Behal
I was doing NCBI BLAST for a sequence and I found that in BLAST result it was matching as Reverse & Complimentary. Is it normal that DNA is matching this way? When we sequence the DNA with 27F...
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A bacterium has been suggested to be grown using a Tungsten lamp with a light intensity of 2,000-3,000 lux. Will it make any difference if the bacteria is grown in light by CFL lamp? What will be...
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Is the method of storage anaerobic bacteria at -80 in Glycerol stock same as that of aerobic bacteria? Will Glycerol prepared in degassed water be able to save bacteria?
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What are the suggested methods for measuring bacterial growth OD in case bacteria starts secreting pigment in broth during growth?
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i have sequences of 16S r DNA. I used then for BLAST. please guide me how to properly use this sequence for publishable analysis. I used Phylip for Tree generation but do not know its full...
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