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Top : New Forum Archives (2009-): : Molecular-Biology
1351. Protein purification. How to make function of recombinant protein? - (reply: 2)
1352. PCR double-bands - (reply: 1)
1353. HELP!! 3 way ligation question - (reply: 1)
1354. BL-21 Gold (DE3) cells and further strains - (reply: 2)
1355. PI needs something ASAP! - densitometry on westerns (reply: 1)
1356. DBA2J genome sequence - (reply: 1)
1357. how can I identify hemi- and homozygous individuals? - (reply: 1)
1358. Question about Primers - (reply: 3)
1359. Odd question. Can I use DNase to decontaminate Primers? - Primer decontamination (reply: 2)
1360. Possible solvents for RNA - (reply: 2)
1361. weird bands after minipreps - molecular cloning (reply: 2)
1362. Large fragment amplification failed - (reply: 3)
1363. purification of PCR product for cloning in a vector - (reply: 3)
1364. elimination of Protein interference from DNA - for RT-PCR (reply: 2)
1365. Transient transfection with viral vectors - Is it acceptable to do direct transfection with viral vectors? (reply: 1)
1366. Adapter ligation problem - (reply: 5)
1367. Primer design with a tag - (reply: 4)
1368. Lithium electrophoresis buffer - Why does it not work? (reply: 2)
1369. Weird migration of double digested plasmid - (reply: 4)
1370. Run agarose/formaldehyde gel for 5 mins before loading samples? Why? - (reply: 1)
1371. Myc tags - (reply: 1)
1372. MOPS: How do you sterlise yours? - (reply: 2)
1373. Which gel concentration - (reply: 4)
1374. Glyoxylated RNA and SYBR Safe - Running glyoxylated RNA on a SYBR safe agarose gel - NO BANDS (reply: 1)
1375. PCR Amplification: Tips on simple things to keep an eye out for - (reply: 1)
1376. MINI Dialysis Units - below 2K MWCO? (reply: 1)
1377. PCR for sequencing genomic DNA (multiple alleles) - Are there preferences for amplification of certain sequences? (reply: 1)
1378. Rotten Fish Smell in TAE Buffer - Stinky TAE (reply: 3)
1379. plasmid extraction and purification - methods to extract and purify plasmid to get high purity super coil (reply: 4)
1380. Combining forward and reverse primer gives different size on gel - (reply: 2)