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Top : New Forum Archives (2009-): : Molecular-Cloning
451. Cloning genetic sequences of proteins. - (reply: 1)
452. problem of restriction enzyme digestion - (reply: 3)
453. Site-directed, PCR works but no colonies - (reply: 2)
454. Simoltanious Multi-restriction digestion - (reply: 3)
455. Using unopened restriction enzyme "expired" in 2010/11 - (reply: 3)
456. can you recommend a gateway mammalian expression vector? Please? :) - (reply: 1)
457. Restriction digestion problems - (reply: 3)
458. should I do blunt end my pcr product before ligation - (reply: 2)
459. Maxiprep of freeze/thawed pellet. - (reply: 1)
460. Digest with AarI and Pml I - (reply: 1)
461. Help with CGL gene cloning problems - (reply: 1)
462. screening for GPF - (reply: 10)
463. Creating a pGEM-T easy + insert sequence map - (reply: 1)
464. where to get vector overexpressing caveolin-1? - (reply: 2)
465. Colony PCR works but DNA yeild very low after miniprep - (reply: 2)
466. pINDUCER series - (reply: 1)
467. LZRS vector details - (reply: 1)
468. 12.4kb vector 6.7kb insert - (reply: 2)
469. Stable transfection - (reply: 2)
470. Using normal competent cells in electroporation method? - (reply: 1)
471. an effective way to do a yeast colony pcr - (reply: 2)
472. pGEM-T Easy vector contamination - (reply: 2)
473. recover old transformed DH5 - (reply: 1)
474. NZY+Broth can be replaced by LB Broth in mutagenesis exp - (reply: 2)
475. oligo(dt) 15 vs random primers - (reply: 3)
476. I need bynary vector pART27 - (reply: 1)
477. Plasmid with two similar bacterial ORIs - Can it be transformed into bacteria?? - (reply: 2)
478. Why don't I get the expected entry clones when I use the gateway system?? - (reply: 2)
479. Need help verifying promotor of a PUC19 based plasmid - (reply: 1)
480. cloning into Pgem t easy - (reply: 1)