|
1591. Bioanalyzer not recognising the chip - chip misaligned/manufacturing problem? - (reply: 4)
1592. transient transfection - (reply: 1)
1593. Bad sequence - (reply: 5)
1594. Southern Blot troubleshooting - Please help (reply: 3)
1595. Removing sequencing migration artefacts - (reply: 1)
1596. What is the minimum DNA concentration requried for double digestion? - (reply: 1)
1597. Probes design for southern-blot - need more information for probes design for southern-blot (reply: 3)
1598. finding promoter - (reply: 1)
1599. Aaaah I want to die!!!! PCR won't work - Why do the extractions that amplified 2 weeks ago fail now? (reply: 13)
1600. Normalizing RNA concentrations prior to cDNA production - qPCR and making cDNA (reply: 1)
1601. precipitation of secreted protein from growth media - (reply: 1)
1602. EMSA gel problem - (reply: 2)
1603. cloning - (reply: 6)
1604. Generating stable cell line - (reply: 2)
1605. Can't get clean RNA prep with TRIzol - (reply: 2)
1606. Sequencing of gene promoter/terminator, when you only have the AA sequence of th - (reply: 2)
1607. vectors maps - (reply: 2)
1608. Fusion of reporter genes - (reply: 2)
1609. reuse electroporation cuvette? - (reply: 4)
1610. PCR Master mix - (reply: 1)
1611. Fake positive colony in lamda RED reconbination, why? - (reply: 2)
1612. Cloning from cDNA - the wrong gene?! - (reply: 2)
1613. Ligation - (reply: 3)
1614. circular or linear pDNA for stable clone generation? - (reply: 1)
1615. failure PCR amplification from low GC content gene - (reply: 5)
1616. recombineering for ES cell targeting - retrieval problems (reply: 1)
1617. different PCR primers for real-time and classic PCR - (reply: 3)
1618. Simple gel question - (reply: 7)
1619. Can I redo a linearization - (reply: 1)
1620. primers deconamination??? - (reply: 6)
1592. transient transfection - (reply: 1)
1593. Bad sequence - (reply: 5)
1594. Southern Blot troubleshooting - Please help (reply: 3)
1595. Removing sequencing migration artefacts - (reply: 1)
1596. What is the minimum DNA concentration requried for double digestion? - (reply: 1)
1597. Probes design for southern-blot - need more information for probes design for southern-blot (reply: 3)
1598. finding promoter - (reply: 1)
1599. Aaaah I want to die!!!! PCR won't work - Why do the extractions that amplified 2 weeks ago fail now? (reply: 13)
1600. Normalizing RNA concentrations prior to cDNA production - qPCR and making cDNA (reply: 1)
1601. precipitation of secreted protein from growth media - (reply: 1)
1602. EMSA gel problem - (reply: 2)
1603. cloning - (reply: 6)
1604. Generating stable cell line - (reply: 2)
1605. Can't get clean RNA prep with TRIzol - (reply: 2)
1606. Sequencing of gene promoter/terminator, when you only have the AA sequence of th - (reply: 2)
1607. vectors maps - (reply: 2)
1608. Fusion of reporter genes - (reply: 2)
1609. reuse electroporation cuvette? - (reply: 4)
1610. PCR Master mix - (reply: 1)
1611. Fake positive colony in lamda RED reconbination, why? - (reply: 2)
1612. Cloning from cDNA - the wrong gene?! - (reply: 2)
1613. Ligation - (reply: 3)
1614. circular or linear pDNA for stable clone generation? - (reply: 1)
1615. failure PCR amplification from low GC content gene - (reply: 5)
1616. recombineering for ES cell targeting - retrieval problems (reply: 1)
1617. different PCR primers for real-time and classic PCR - (reply: 3)
1618. Simple gel question - (reply: 7)
1619. Can I redo a linearization - (reply: 1)
1620. primers deconamination??? - (reply: 6)