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Top : New Forum Archives (2009-): : Molecular-Biology
1411. STADEN PACKAGE - Problems with Installing staden on MAC (reply: 3)
1412. Migration Distance on a Gel - (reply: 2)
1413. Calculating Primer concentrations for PCR - Is there an easy way to do this...help (reply: 3)
1414. DNA isolation from plant nuclei by plasmid extraction kit - (reply: 1)
1415. BAC isolation - (reply: 2)
1416. Restriction mapping - (reply: 3)
1417. DNA isolation from human serum/plasma - (reply: 1)
1418. Viral DNA extraction - (reply: 1)
1419. Wrong pcr product size - (reply: 4)
1420. Making solutions for RNA work - (reply: 1)
1421. RNA quality - (reply: 3)
1422. gDNA restriction digest - (reply: 1)
1423. why most Annexin 5 products are conjugated? - Can't we use it on its own? (reply: 7)
1424. Cloning long fragment...got lots of colonies with vectors that have no inserts.. - (reply: 9)
1425. Promoter "optimization" - (reply: 1)
1426. Adding Restriction Site to DNA - (reply: 3)
1427. how to do gel documentation - (reply: 2)
1428. DNA ext from paraffin-embedded tissue ... a dilemma ! - FFPE tissue refuse to lyse strange whitish clumps formed!! (reply: 1)
1429. Glycine linker - (reply: 2)
1430. Why does the amount of plamids transformed affect colony count? - (reply: 2)
1431. How to obatin intron sequence from cDNA sequence? - (reply: 1)
1432. genomic DNA extraction - why there appears a smear on the gel photo (reply: 11)
1433. Colony Pcr - primers - (reply: 5)
1434. cloning more than 1 gene into vector if no IRES available - Xenopus IRES? if not, what to do? (reply: 2)
1435. iCODEHOP help: how are the reverse primers supposed to be read? - Degenerate primer design (reply: 1)
1436. Sequence size and insert size - Sequence size has larger base pair than insert size (reply: 2)
1437. QCMD samples - (reply: 5)
1438. competent cells - OD600 reading (reply: 6)
1439. Creating overhangs with PCR - (reply: 4)
1440. RNA: Is this degratation or something else? - (reply: 1)