5 Questions 53 Answers 0 Followers
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...
07 July 2014 570 11 View
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...
06 June 2014 1,510 3 View
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?
05 May 2014 4,010 8 View
What are the suggested methods for measuring bacterial growth OD in case bacteria starts secreting pigment in broth during growth?
05 May 2014 9,926 6 View
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...
02 February 2012 9,127 4 View
