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