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Questions related from Dipanshu Ghosh
I am willing to do some kind experiments on Picrorhiza kurroa and for the same I need seeds.
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When I elute out DNA for cloning purpose, on measuring nano drop reading I get very low value of A 260/230 (it's like 0.04 or 0.08 and so). Even after repeated washing of column this problem...
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I am getting appritiable growth of bacteria in antibiotic medium. On isolating plasmid by conventional method or by kit I am getting either very little amount of plamids or no plasmids or...
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As we know when we treat a protein with SDS, it breaks non covalent bonds to form primary structure. But how it adds negative charges uniformly on all constituent amino acids?
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I am trying to prepare Bradford reagent in lab. When I'm adding 95% ethanol to commisse blue G250 dye to dissolve it, the solution is turning blue. Does it indicate to any problem in Bradford...
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I want to clone a 3kb DNA fragment into pGEMT EASY. On gel I can see 3kb band but I can't clone it into pGEMT EASY. Can anyone suggest how I can troubleshoot?
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