Protocol Online logo
Top : New Forum Archives (2009-): : Molecular-Biology
571. Why do only some nuclear lysis buffers create DNA 'goop' - (reply: 1)
572. Continuous growth of E. coli on AMP LB plate - (reply: 2)
573. Plasmid compatibly groups - (reply: 5)
574. too much DNA on agarose gel - (reply: 10)
575. What are the "mammalian vectors N1 and C1"? - (reply: 1)
576. Life before BLAST etc? Help needed... - (reply: 1)
577. How base pairs upstream of gene to include for the promoter? - (reply: 3)
578. Neomycin resistance sequence - (reply: 1)
579. Can I use Real-time PCR instead of Southern Blot to determine number of integran - (reply: 1)
580. polyacrylamide RNA gel - (reply: 4)
581. Making a standard curve from bacterial suspensions - (reply: 1)
582. Is my RNA degraded? - (reply: 7)
583. Phosphotyrosine western blotting, HELP! - (reply: 1)
584. Bacteriophage genome extraction - (reply: 1)
585. Fast, cheap and dependable DNA extraction protocol for students? - (reply: 3)
586. western blot troubleshooting - (reply: 5)
587. Sanger Sequencing RNAse Interference? - (reply: 1)
588. isolating DNA from cells in suspension - (reply: 5)
589. survival strategy of bacteria - (reply: 4)
590. can restriction enzymes be stored at -70C? - (reply: 3)
591. Sequencing Primers and Plasmids - (reply: 3)
592. Dam Dcm Negative Strain - (reply: 2)
593. Restriction Enzymes - (reply: 4)
594. RNA isolation - (reply: 1)
595. Qiagen re using column - (reply: 5)
596. Low yield for small RNA isolation - (reply: 1)
597. Primers to amplify Kan operon from pet28 - (reply: 2)
598. Questions about proper technical approach - (reply: 6)
599. RNA extraction: low RCF by mistake - (reply: 1)
600. Avoid SDS in thermal lysis: whole blood? - (reply: 1)