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Questions related from Lalit Meena
The terminal portion of the RNA can be identified but how can I design primer of middle part of the RNA?
12 December 2014 8,443 1 View
Since the size is a bit larger (9.7 kb) I have to clone it in fragments (subcloning). Overlap primers can be designed for PCR amplification.
12 December 2014 7,855 3 View
i have designed degenerate primer and amplified product (700 bp) is cloned and sequenced. but now how can i proceed for for cloning of rest (9.0kb) of the the genome.....
12 December 2014 7,141 5 View
Is it true in all cases of NPs formulations or not?
03 March 2014 1,198 2 View
micro RNA identification
09 September 2012 425 8 View