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Top : New Forum Archives (2009-): : Molecular-Cloning
301. In-fusion HD cloning - (reply: 3)
302. Is there a such thing that would allow me to generate 2 individual proteins, but - (reply: 5)
303. Few colonies frm sticky end cloning - (reply: 3)
304. transformation problem - (reply: 8)
305. Problems with Digestion? - (reply: 7)
306. plasmid digestion - problem with enzymes? - (reply: 4)
307. Problem with cloning - (reply: 7)
308. double transformation problem - (reply: 3)
309. Too many negative clones using Directional TOPO Cloning - (reply: 5)
310. competent cells - (reply: 1)
311. "Easiest" sticky end combination - (reply: 3)
312. Cloning advice - (reply: 3)
313. classic cloning with restriction enzymes into empty pcDNA3.1D - (reply: 1)
314. Cloning large fragments - (reply: 9)
315. Transformation colonies does not contain insert - (reply: 3)
316. Blunt cloning - No insert, despite lots of colonies - (reply: 3)
317. Need urgent advise.. - (reply: 3)
318. Cloning Mitochondrial Targeting Sequence - (reply: 4)
319. problem in cloning - (reply: 2)
320. TA cloning: ligation problem or toxic construct? - (reply: 4)
321. Reappearing band shifts/smears after double digest and gel purification - (reply: 2)
322. Do I need to sequence after digestion? - (reply: 9)
323. quick change mutagenesis...... - (reply: 15)
324. Problem with double digestion: one enzyme is not working - (reply: 8)
325. Transient Transfection Controls (Gateway Technology) - (reply: 4)
326. Problems with crossover PCR - (reply: 2)
327. gateway destination vector grows on kanamycin plates !!!!! - (reply: 1)
328. Two genes, same MCS - (reply: 1)
329. Including ATG in cloning? - (reply: 1)
330. Plasmid Extraction from P. Aeruginosa smears in Gel! - (reply: 2)