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Top : New Forum Archives (2009-): : Molecular-Biology
1561. Calculating Primer concentrations for PCR - Is there an easy way to do this...help (reply: 3)
1562. DNA isolation from plant nuclei by plasmid extraction kit - (reply: 1)
1563. BAC isolation - (reply: 2)
1564. Restriction mapping - (reply: 3)
1565. DNA isolation from human serum/plasma - (reply: 1)
1566. Viral DNA extraction - (reply: 1)
1567. Wrong pcr product size - (reply: 4)
1568. Making solutions for RNA work - (reply: 1)
1569. RNA quality - (reply: 3)
1570. gDNA restriction digest - (reply: 1)
1571. why most Annexin 5 products are conjugated? - Can't we use it on its own? (reply: 7)
1572. Cloning long fragment...got lots of colonies with vectors that have no inserts.. - (reply: 9)
1573. Promoter "optimization" - (reply: 1)
1574. Adding Restriction Site to DNA - (reply: 3)
1575. how to do gel documentation - (reply: 2)
1576. DNA ext from paraffin-embedded tissue ... a dilemma ! - FFPE tissue refuse to lyse strange whitish clumps formed!! (reply: 1)
1577. Glycine linker - (reply: 2)
1578. Why does the amount of plamids transformed affect colony count? - (reply: 2)
1579. How to obatin intron sequence from cDNA sequence? - (reply: 1)
1580. genomic DNA extraction - why there appears a smear on the gel photo (reply: 11)
1581. Colony Pcr - primers - (reply: 5)
1582. cloning more than 1 gene into vector if no IRES available - Xenopus IRES? if not, what to do? (reply: 2)
1583. iCODEHOP help: how are the reverse primers supposed to be read? - Degenerate primer design (reply: 1)
1584. Sequence size and insert size - Sequence size has larger base pair than insert size (reply: 2)
1585. QCMD samples - (reply: 5)
1586. competent cells - OD600 reading (reply: 6)
1587. Creating overhangs with PCR - (reply: 4)
1588. RNA: Is this degratation or something else? - (reply: 1)
1589. regenerate qiagen midi columns - how to reuse the midiprep DNA columns (reply: 3)
1590. Is there any software that can be sued to design degenerate primers - (reply: 1)