Protocol Online logo
Top : New Forum Archives (2009-): : Molecular-Cloning
331. How to avoid RNA contamination in DNA samples:? - (reply: 1)
332. Wavy Lines in Gel - (reply: 2)
333. Question Relating to LacZ Disruption - (reply: 4)
334. Recombinant Plasmid is not being amplified in transformed cells - (reply: 2)
335. Site directed mutagenesis - (reply: 5)
336. PCR insert - in frame? - (reply: 2)
337. Whole plasmid amplification by PCR - (reply: 2)
338. colony PCR after transformation - (reply: 1)
339. For promoter assay, which vector I should use? - (reply: 5)
340. Sequencing of the cloned plasmid - (reply: 5)
341. 4 way cloning into TA Vector - (reply: 10)
342. I get band double the size what does it mean - (reply: 3)
343. What are the elements of a BAC that differentiate it from a regular plasmid - (reply: 1)
344. Neeed Help , cloning Confirmation ?! - (reply: 5)
345. Puzzling Cloning Problem With a Specific Vector - (reply: 1)
346. Can I quantify restricted plasmid and oligos? - (reply: 3)
347. Pseudomonas aeruginosa 14 with pUC19? - (reply: 2)
348. Use magnetic beads to purify restriction enzyme digestion product - (reply: 1)
349. TOPO TA ligation problems - (reply: 6)
350. Luciferase assay problem - (reply: 2)
351. Double digestion with BamHI and BglII - (reply: 4)
352. nicked linear DNA - (reply: 5)
353. Selection of E.coli competent cells - (reply: 2)
354. Double strand cdna synthysis - (reply: 4)
355. mutagenic primers with very high GC content. - (reply: 3)
356. TA Cloning of ds cDNA - (reply: 6)
357. Promoter distance from ATG - (reply: 3)
358. Measuring Fluorescene of RFP - (reply: 7)
359. Smallest possible insert size for Ligation reaction - (reply: 2)
360. Very difficult cloning project - how to clone something that is not compatible w - (reply: 4)