Protocol Online logo
Top : New Forum Archives (2009-): : Molecular-Biology
1861. transient transfection - (reply: 1)
1862. Bad sequence - (reply: 5)
1863. Southern Blot troubleshooting - Please help (reply: 3)
1864. Removing sequencing migration artefacts - (reply: 1)
1865. What is the minimum DNA concentration requried for double digestion? - (reply: 1)
1866. Probes design for southern-blot - need more information for probes design for southern-blot (reply: 3)
1867. finding promoter - (reply: 1)
1868. Aaaah I want to die!!!! PCR won't work - Why do the extractions that amplified 2 weeks ago fail now? (reply: 13)
1869. Normalizing RNA concentrations prior to cDNA production - qPCR and making cDNA (reply: 1)
1870. precipitation of secreted protein from growth media - (reply: 1)
1871. EMSA gel problem - (reply: 2)
1872. cloning - (reply: 6)
1873. Generating stable cell line - (reply: 2)
1874. Can't get clean RNA prep with TRIzol - (reply: 2)
1875. Sequencing of gene promoter/terminator, when you only have the AA sequence of th - (reply: 2)
1876. vectors maps - (reply: 2)
1877. Fusion of reporter genes - (reply: 2)
1878. reuse electroporation cuvette? - (reply: 4)
1879. PCR Master mix - (reply: 1)
1880. Fake positive colony in lamda RED reconbination, why? - (reply: 2)
1881. Cloning from cDNA - the wrong gene?! - (reply: 2)
1882. Ligation - (reply: 3)
1883. circular or linear pDNA for stable clone generation? - (reply: 1)
1884. failure PCR amplification from low GC content gene - (reply: 5)
1885. recombineering for ES cell targeting - retrieval problems (reply: 1)
1886. different PCR primers for real-time and classic PCR - (reply: 3)
1887. Simple gel question - (reply: 7)
1888. Can I redo a linearization - (reply: 1)
1889. primers deconamination??? - (reply: 6)
1890. Help in SDS PAGE - Molecular Biology (reply: 3)