Protocol Online logo
Top : New Forum Archives (2009-): : Molecular-Biology
661. Help with PCR and Gel Electrophoresis. Not getting any bands - (reply: 8)
662. Making a qPCR standard amplicon from cloning, why? - (reply: 4)
663. QIAquick Gel Extraction - (reply: 2)
664. Hypo-osmotic lysisbuffer for "purification" of mitochondria. - (reply: 5)
665. If Colony plated on plate coming below agar, is it contamination? - (reply: 13)
666. Why GFP gets cutted from my fusion protein? - (reply: 9)
667. Mutations and Evolution - (reply: 15)
668. Dissolving DNA - finding better techniques - (reply: 12)
669. Southern blotting - (reply: 2)
670. help ,blunt end ligation - (reply: 4)
671. FLP-FRT recombination - (reply: 1)
672. GST fusion protein purification - (reply: 2)
673. Can human 18S primer, probe set for qPCR be used for Rhesus and Cynomolgus sampl - (reply: 3)
674. Dual Luciferase assay data analysis issues - (reply: 4)
675. DNA sequencing after ligation! HELP! - (reply: 8)
676. isolation of plasmid (midi and maxi prep) - (reply: 18)
677. Low 260/230 ratio depending on tissue. - (reply: 4)
678. can we extract DNA from snap freeze tissue - (reply: 2)
679. About Hot Start Taq DNA Polymerases - (reply: 2)
680. RNA integrity - (reply: 5)
681. my pcr product is larger than expected - (reply: 4)
682. Midi and Maxi prep - (reply: 3)
683. Question about PCR - DNA or RNA as template - (reply: 4)
684. Dyes for RNA in Urea-polyacrylamide gel - (reply: 1)
685. Do Qiagen RNeasy spin columns expire? - (reply: 1)
686. pcr purification - (reply: 1)
687. E. coli strain for conjugation - (reply: 1)
688. Incorporating RNAse A into DNA extraction - (reply: 2)
689. How to clone insert with one sticky and one blunt end into vector? - (reply: 1)
690. PCR band moves lower than its size on agarose gel - (reply: 3)