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1591. short question - FDG staining (reply: 2)
1592. 6.7%Polyacrylamide/50% Urea gel - (reply: 1)
1593. STADEN PACKAGE - Problems with Installing staden on MAC (reply: 3)
1594. Migration Distance on a Gel - (reply: 2)
1595. Calculating Primer concentrations for PCR - Is there an easy way to do this...help (reply: 3)
1596. DNA isolation from plant nuclei by plasmid extraction kit - (reply: 1)
1597. BAC isolation - (reply: 2)
1598. Restriction mapping - (reply: 3)
1599. DNA isolation from human serum/plasma - (reply: 1)
1600. Viral DNA extraction - (reply: 1)
1601. Wrong pcr product size - (reply: 4)
1602. Making solutions for RNA work - (reply: 1)
1603. RNA quality - (reply: 3)
1604. gDNA restriction digest - (reply: 1)
1605. why most Annexin 5 products are conjugated? - Can't we use it on its own? (reply: 7)
1606. Cloning long fragment...got lots of colonies with vectors that have no inserts.. - (reply: 9)
1607. Promoter "optimization" - (reply: 1)
1608. Adding Restriction Site to DNA - (reply: 3)
1609. how to do gel documentation - (reply: 2)
1610. DNA ext from paraffin-embedded tissue ... a dilemma ! - FFPE tissue refuse to lyse strange whitish clumps formed!! (reply: 1)
1611. Glycine linker - (reply: 2)
1612. Why does the amount of plamids transformed affect colony count? - (reply: 2)
1613. How to obatin intron sequence from cDNA sequence? - (reply: 1)
1614. genomic DNA extraction - why there appears a smear on the gel photo (reply: 11)
1615. Colony Pcr - primers - (reply: 5)
1616. cloning more than 1 gene into vector if no IRES available - Xenopus IRES? if not, what to do? (reply: 2)
1617. iCODEHOP help: how are the reverse primers supposed to be read? - Degenerate primer design (reply: 1)
1618. Sequence size and insert size - Sequence size has larger base pair than insert size (reply: 2)
1619. QCMD samples - (reply: 5)
1620. competent cells - OD600 reading (reply: 6)
1592. 6.7%Polyacrylamide/50% Urea gel - (reply: 1)
1593. STADEN PACKAGE - Problems with Installing staden on MAC (reply: 3)
1594. Migration Distance on a Gel - (reply: 2)
1595. Calculating Primer concentrations for PCR - Is there an easy way to do this...help (reply: 3)
1596. DNA isolation from plant nuclei by plasmid extraction kit - (reply: 1)
1597. BAC isolation - (reply: 2)
1598. Restriction mapping - (reply: 3)
1599. DNA isolation from human serum/plasma - (reply: 1)
1600. Viral DNA extraction - (reply: 1)
1601. Wrong pcr product size - (reply: 4)
1602. Making solutions for RNA work - (reply: 1)
1603. RNA quality - (reply: 3)
1604. gDNA restriction digest - (reply: 1)
1605. why most Annexin 5 products are conjugated? - Can't we use it on its own? (reply: 7)
1606. Cloning long fragment...got lots of colonies with vectors that have no inserts.. - (reply: 9)
1607. Promoter "optimization" - (reply: 1)
1608. Adding Restriction Site to DNA - (reply: 3)
1609. how to do gel documentation - (reply: 2)
1610. DNA ext from paraffin-embedded tissue ... a dilemma ! - FFPE tissue refuse to lyse strange whitish clumps formed!! (reply: 1)
1611. Glycine linker - (reply: 2)
1612. Why does the amount of plamids transformed affect colony count? - (reply: 2)
1613. How to obatin intron sequence from cDNA sequence? - (reply: 1)
1614. genomic DNA extraction - why there appears a smear on the gel photo (reply: 11)
1615. Colony Pcr - primers - (reply: 5)
1616. cloning more than 1 gene into vector if no IRES available - Xenopus IRES? if not, what to do? (reply: 2)
1617. iCODEHOP help: how are the reverse primers supposed to be read? - Degenerate primer design (reply: 1)
1618. Sequence size and insert size - Sequence size has larger base pair than insert size (reply: 2)
1619. QCMD samples - (reply: 5)
1620. competent cells - OD600 reading (reply: 6)