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Molecular-Cloning
691.
Why do double digest (XhoI & SacI) of NEB use buffer 1 ? -
(reply: 4)
692.
How to design RT-PCR primers in-frame for expression vector? -
(reply: 1)
693.
Blue colonies with insert, white colonies with multiple weak bands -
(reply: 5)
694.
Plasmid digestion after transformation -
(reply: 4)
695.
Blunt end ligation insert:vector ratio -
(reply: 1)
696.
PCRed on restriction sites -- how do I purify it? -
(reply: 8)
697.
Puzzle about plamid and its digest, plz help -
(reply: 8)
698.
Smear above plasmid dna -
(reply: 3)
699.
restriction digestion buffers contaminated with dnase -
(reply: 3)
700.
Bacterial Induction -
(reply: 1)
701.
purification of digested vector by agarose eletrophoresis problem -
(reply: 4)
702.
smear restriction digest -
(reply: 1)
703.
How to set the Sonicator to 20%amplitude? -
(reply: 3)
704.
No DNA after midiprep -
(reply: 2)
705.
plasmid construction where I have to replace the chloramphenicol with kanamycin -
(reply: 6)
706.
Is Kozak's full sequence necessary? or just ACCATG is enough? -
(reply: 4)
707.
how to store LB-agar-antibiotic- X-gal-IPTG plate -
(reply: 3)
708.
Impact of primer sequence on TA cloning -
(reply: 3)
709.
Maximum length of cDNA from RT reaction -
(reply: 6)
710.
overlapping PCR protocol -
(reply: 12)
711.
cloning an AT rich gene -
(reply: 3)
712.
Cloning two genes in the same plasmid -
(reply: 4)
713.
How to wipe out fragment of dead cells from the suspension cells? -
(reply: 1)
714.
why my solution II turns cloudy during plasmid extraction? -
(reply: 6)
715.
Problem: Cloning DNA shuffled band -
(reply: 2)
716.
shRNA to primary keratinocytes -
(reply: 1)
717.
Enzymetic digestion with ApaI and HincII -
(reply: 2)
718.
Ligation gel picture interpretation -
(reply: 4)
719.
strange subcloning problem -
(reply: 9)
720.
Cloned sequence is not predicted size by western blot -
(reply: 1)
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