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