Protocol Online logo
Top : New Forum Archives (2009-): : Molecular-Biology
1561. Wrong pcr product size - (reply: 4)
1562. Making solutions for RNA work - (reply: 1)
1563. RNA quality - (reply: 3)
1564. gDNA restriction digest - (reply: 1)
1565. why most Annexin 5 products are conjugated? - Can't we use it on its own? (reply: 7)
1566. Cloning long fragment...got lots of colonies with vectors that have no inserts.. - (reply: 9)
1567. Promoter "optimization" - (reply: 1)
1568. Adding Restriction Site to DNA - (reply: 3)
1569. how to do gel documentation - (reply: 2)
1570. DNA ext from paraffin-embedded tissue ... a dilemma ! - FFPE tissue refuse to lyse strange whitish clumps formed!! (reply: 1)
1571. Glycine linker - (reply: 2)
1572. Why does the amount of plamids transformed affect colony count? - (reply: 2)
1573. How to obatin intron sequence from cDNA sequence? - (reply: 1)
1574. genomic DNA extraction - why there appears a smear on the gel photo (reply: 11)
1575. Colony Pcr - primers - (reply: 5)
1576. cloning more than 1 gene into vector if no IRES available - Xenopus IRES? if not, what to do? (reply: 2)
1577. iCODEHOP help: how are the reverse primers supposed to be read? - Degenerate primer design (reply: 1)
1578. Sequence size and insert size - Sequence size has larger base pair than insert size (reply: 2)
1579. QCMD samples - (reply: 5)
1580. competent cells - OD600 reading (reply: 6)
1581. Creating overhangs with PCR - (reply: 4)
1582. RNA: Is this degratation or something else? - (reply: 1)
1583. regenerate qiagen midi columns - how to reuse the midiprep DNA columns (reply: 3)
1584. Is there any software that can be sued to design degenerate primers - (reply: 1)
1585. Primer Decontamination - (reply: 2)
1586. PGem Easy Vector System: ampicillin conc and plasmid length problem - (reply: 10)
1587. mRNA preparation from total RNA - a role of poly A in mRNA preparation from total RNA (reply: 2)
1588. How long is "overnight"? - (reply: 3)
1589. Trizol stability - (reply: 1)
1590. DNA stuck in gel well - some samples are stuck in the agarose-gel well and don't migrate (reply: 4)