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Top : New Forum Archives (2009-): : Molecular-Cloning
271. self ligation - (reply: 1)
272. Ligation/Transformation Mess-up, are they going to survive? - (reply: 5)
273. Cloning large transgenes - (reply: 2)
274. In-fusion HD cloning - (reply: 3)
275. Is there a such thing that would allow me to generate 2 individual proteins, but - (reply: 5)
276. Few colonies frm sticky end cloning - (reply: 3)
277. transformation problem - (reply: 8)
278. Problems with Digestion? - (reply: 7)
279. plasmid digestion - problem with enzymes? - (reply: 4)
280. Problem with cloning - (reply: 7)
281. double transformation problem - (reply: 3)
282. Too many negative clones using Directional TOPO Cloning - (reply: 5)
283. competent cells - (reply: 1)
284. "Easiest" sticky end combination - (reply: 3)
285. Cloning advice - (reply: 3)
286. classic cloning with restriction enzymes into empty pcDNA3.1D - (reply: 1)
287. Cloning large fragments - (reply: 9)
288. Transformation colonies does not contain insert - (reply: 3)
289. Blunt cloning - No insert, despite lots of colonies - (reply: 3)
290. Need urgent advise.. - (reply: 3)
291. Cloning Mitochondrial Targeting Sequence - (reply: 4)
292. problem in cloning - (reply: 2)
293. TA cloning: ligation problem or toxic construct? - (reply: 4)
294. Reappearing band shifts/smears after double digest and gel purification - (reply: 2)
295. Do I need to sequence after digestion? - (reply: 9)
296. quick change mutagenesis...... - (reply: 15)
297. Problem with double digestion: one enzyme is not working - (reply: 8)
298. Transient Transfection Controls (Gateway Technology) - (reply: 4)
299. Problems with crossover PCR - (reply: 2)
300. gateway destination vector grows on kanamycin plates !!!!! - (reply: 1)