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