2341. How to deionize water ? - (reply: 1)
2342. pCMVneo - need a description, company or plasmid map (reply: 2)
2343. Is my RNA dead? - freezing cells after adding RNA lysis buffer (reply: 2)
2344. PEG for ligation - just filtered by 0.2um filtered (reply: 3)
2345. RNAse and DNA digestion in Southern Blot - (reply: 3)
2346. is there a loss of volume after pcr? - (reply: 5)
2347. why protein gels are run at constant current and constant voltage? - (reply: 2)
2348. Problem with directed mutagensis - (reply: 9)
2349. kinase - kinase activity (reply: 6)
2350. GFP to expression - (reply: 3)
2351. Enzyme Site in reverse Primer - (reply: 3)
2352. BAC DNA restriction analysis - I need help :( (reply: 4)
2353. help as to why there are no bands when running my PCR product - (reply: 3)
2354. general pcr/primer question - (reply: 1)
2355. deP for cloning - Dephosphorilation (reply: 5)
2356. Sequencing from Minipreps - Is it possible to sequence directly from minipreps? (reply: 14)
2357. Is multiple freezing-thawing harmful to cDNA? - (reply: 3)
2358. 2 PCR product to be inserted into 1 expression vector - (reply: 2)
2359. Need a FRET PCR protocol - (reply: 1)
2360. RACE problems - 5-terminal amplication (reply: 1)
2361. for the PCR primer what is better the hairpin or the self annealing? - (reply: 9)
2362. transcription in prokaryotes. - is whole shine-dalgarno sequence required? (reply: 1)
2363. Uncut genomic DNA - Migrate through the gel (reply: 3)
2364. Uncut plasmid DNA - (reply: 6)
2365. Using Picogreen to quantitate DNA - Questions about how to make this work! (reply: 2)
2366. analysis of DNA using BamH1 and agarose gel electrophoresis - interpretation of results! (reply: 5)
2367. DNA isolation kits - (reply: 4)
2368. What do you mean by other letters aside from A, C, G, and T in DNA sequencing r - (reply: 3)
2369. RT-PCR Troubles.. - (reply: 3)
2370. Bad sequences - (reply: 6)

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