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Top : New Forum Archives (2009-): : Molecular-Cloning
331. Cloning large transgenes - (reply: 2)
332. In-fusion HD cloning - (reply: 3)
333. Is there a such thing that would allow me to generate 2 individual proteins, but - (reply: 5)
334. Few colonies frm sticky end cloning - (reply: 3)
335. transformation problem - (reply: 8)
336. Problems with Digestion? - (reply: 7)
337. plasmid digestion - problem with enzymes? - (reply: 4)
338. Problem with cloning - (reply: 7)
339. double transformation problem - (reply: 3)
340. Too many negative clones using Directional TOPO Cloning - (reply: 5)
341. competent cells - (reply: 1)
342. "Easiest" sticky end combination - (reply: 3)
343. Cloning advice - (reply: 3)
344. classic cloning with restriction enzymes into empty pcDNA3.1D - (reply: 1)
345. Cloning large fragments - (reply: 9)
346. Transformation colonies does not contain insert - (reply: 3)
347. Blunt cloning - No insert, despite lots of colonies - (reply: 3)
348. Need urgent advise.. - (reply: 3)
349. Cloning Mitochondrial Targeting Sequence - (reply: 4)
350. problem in cloning - (reply: 2)
351. TA cloning: ligation problem or toxic construct? - (reply: 4)
352. Reappearing band shifts/smears after double digest and gel purification - (reply: 2)
353. Do I need to sequence after digestion? - (reply: 9)
354. quick change mutagenesis...... - (reply: 15)
355. Problem with double digestion: one enzyme is not working - (reply: 8)
356. Transient Transfection Controls (Gateway Technology) - (reply: 4)
357. Problems with crossover PCR - (reply: 2)
358. gateway destination vector grows on kanamycin plates !!!!! - (reply: 1)
359. Two genes, same MCS - (reply: 1)
360. Including ATG in cloning? - (reply: 1)