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Top : New Forum Archives (2009-): : Molecular-Cloning
361. In-fusion HD cloning - (reply: 3)
362. Is there a such thing that would allow me to generate 2 individual proteins, but - (reply: 5)
363. Few colonies frm sticky end cloning - (reply: 3)
364. transformation problem - (reply: 8)
365. Problems with Digestion? - (reply: 7)
366. plasmid digestion - problem with enzymes? - (reply: 4)
367. Problem with cloning - (reply: 7)
368. double transformation problem - (reply: 3)
369. Too many negative clones using Directional TOPO Cloning - (reply: 5)
370. competent cells - (reply: 1)
371. "Easiest" sticky end combination - (reply: 3)
372. Cloning advice - (reply: 3)
373. classic cloning with restriction enzymes into empty pcDNA3.1D - (reply: 1)
374. Cloning large fragments - (reply: 9)
375. Transformation colonies does not contain insert - (reply: 3)
376. Blunt cloning - No insert, despite lots of colonies - (reply: 3)
377. Need urgent advise.. - (reply: 3)
378. Cloning Mitochondrial Targeting Sequence - (reply: 4)
379. problem in cloning - (reply: 2)
380. TA cloning: ligation problem or toxic construct? - (reply: 4)
381. Reappearing band shifts/smears after double digest and gel purification - (reply: 2)
382. Do I need to sequence after digestion? - (reply: 9)
383. quick change mutagenesis...... - (reply: 15)
384. Problem with double digestion: one enzyme is not working - (reply: 8)
385. Transient Transfection Controls (Gateway Technology) - (reply: 4)
386. Problems with crossover PCR - (reply: 2)
387. gateway destination vector grows on kanamycin plates !!!!! - (reply: 1)
388. Two genes, same MCS - (reply: 1)
389. Including ATG in cloning? - (reply: 1)
390. Plasmid Extraction from P. Aeruginosa smears in Gel! - (reply: 2)