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Top : New Forum Archives (2009-): : Molecular-Biology
1591. Wrong pcr product size - (reply: 4)
1592. Making solutions for RNA work - (reply: 1)
1593. RNA quality - (reply: 3)
1594. gDNA restriction digest - (reply: 1)
1595. why most Annexin 5 products are conjugated? - Can't we use it on its own? (reply: 7)
1596. Cloning long fragment...got lots of colonies with vectors that have no inserts.. - (reply: 9)
1597. Promoter "optimization" - (reply: 1)
1598. Adding Restriction Site to DNA - (reply: 3)
1599. how to do gel documentation - (reply: 2)
1600. DNA ext from paraffin-embedded tissue ... a dilemma ! - FFPE tissue refuse to lyse strange whitish clumps formed!! (reply: 1)
1601. Glycine linker - (reply: 2)
1602. Why does the amount of plamids transformed affect colony count? - (reply: 2)
1603. How to obatin intron sequence from cDNA sequence? - (reply: 1)
1604. genomic DNA extraction - why there appears a smear on the gel photo (reply: 11)
1605. Colony Pcr - primers - (reply: 5)
1606. cloning more than 1 gene into vector if no IRES available - Xenopus IRES? if not, what to do? (reply: 2)
1607. iCODEHOP help: how are the reverse primers supposed to be read? - Degenerate primer design (reply: 1)
1608. Sequence size and insert size - Sequence size has larger base pair than insert size (reply: 2)
1609. QCMD samples - (reply: 5)
1610. competent cells - OD600 reading (reply: 6)
1611. Creating overhangs with PCR - (reply: 4)
1612. RNA: Is this degratation or something else? - (reply: 1)
1613. regenerate qiagen midi columns - how to reuse the midiprep DNA columns (reply: 3)
1614. Is there any software that can be sued to design degenerate primers - (reply: 1)
1615. Primer Decontamination - (reply: 2)
1616. PGem Easy Vector System: ampicillin conc and plasmid length problem - (reply: 10)
1617. mRNA preparation from total RNA - a role of poly A in mRNA preparation from total RNA (reply: 2)
1618. How long is "overnight"? - (reply: 3)
1619. Trizol stability - (reply: 1)
1620. DNA stuck in gel well - some samples are stuck in the agarose-gel well and don't migrate (reply: 4)