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