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Top : New Forum Archives (2009-): : Molecular-Biology
1381. problem in protein purification - (reply: 5)
1382. Retroviral transduction of T cells - (reply: 4)
1383. strange problem in PAGE gel - (reply: 12)
1384. DNA contamination of RNA samples for qPCR...weird results! - (reply: 3)
1385. Gene targeting - (reply: 3)
1386. PCR product too short - (reply: 6)
1387. Anyone know the margin of error for PCR amplicon size visualized on an agarose g - Margin of Error (reply: 2)
1388. When do I add selection? - (reply: 2)
1389. How to prevent concatemerization during ligation reaction? - (reply: 2)
1390. Washing RNA pellet - 85% ethanol? - (reply: 2)
1391. Viral RNA is relatively stable than mRNA from cells? - (reply: 1)
1392. Unsuccessful cloning with one sticky end & one blunt end - Low transformation efficiency & colonies do not contain insert (reply: 8)
1393. White colonies no insert - (reply: 2)
1394. any strategy to insert MCS into a specific region without any restriction sites - (reply: 5)
1395. Isolating bacterial RNA and protein from the host tissue sample - (reply: 3)
1396. DOT BLOT for pcr product - No result obtain (reply: 1)
1397. Backwards electrophoresis electrodes - Can you dig it? (reply: 1)
1398. Do plasmids work in bacteria? - (reply: 1)
1399. Smears above ribosomal RNA bands - RNA extraction from microalgae (reply: 2)
1400. CEN sequences on plasmids (yeast) - (reply: 4)
1401. DMSO - (reply: 1)
1402. Trizol Extraction of PBMCs, low 260/230 - (reply: 5)
1403. PCR amplification with Pfu / quality of DNA - (reply: 4)
1404. primer design - (reply: 2)
1405. recombinant ecoli in log phase overnight media suggestion - (reply: 2)
1406. TRIzol phase extraction with Lock-Phase tubes - Does anyone use Lock-Phase? (reply: 1)
1407. help! quikchange mutagenesis kit - (reply: 1)
1408. T7 terminator-modification - (reply: 2)
1409. Tissue homogenization buffer to keep viral RNA intact - (reply: 6)
1410. ORI names - name of a plasmid ori (reply: 11)