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Top : New Forum Archives (2009-): : Molecular-Biology
601. Making a qPCR standard amplicon from cloning, why? - (reply: 4)
602. QIAquick Gel Extraction - (reply: 2)
603. Hypo-osmotic lysisbuffer for "purification" of mitochondria. - (reply: 5)
604. If Colony plated on plate coming below agar, is it contamination? - (reply: 13)
605. Why GFP gets cutted from my fusion protein? - (reply: 9)
606. Mutations and Evolution - (reply: 15)
607. Dissolving DNA - finding better techniques - (reply: 12)
608. Southern blotting - (reply: 2)
609. help ,blunt end ligation - (reply: 4)
610. FLP-FRT recombination - (reply: 1)
611. GST fusion protein purification - (reply: 2)
612. Can human 18S primer, probe set for qPCR be used for Rhesus and Cynomolgus sampl - (reply: 3)
613. Dual Luciferase assay data analysis issues - (reply: 4)
614. DNA sequencing after ligation! HELP! - (reply: 8)
615. isolation of plasmid (midi and maxi prep) - (reply: 18)
616. Low 260/230 ratio depending on tissue. - (reply: 4)
617. can we extract DNA from snap freeze tissue - (reply: 2)
618. About Hot Start Taq DNA Polymerases - (reply: 2)
619. RNA integrity - (reply: 5)
620. my pcr product is larger than expected - (reply: 4)
621. Midi and Maxi prep - (reply: 3)
622. Question about PCR - DNA or RNA as template - (reply: 4)
623. Dyes for RNA in Urea-polyacrylamide gel - (reply: 1)
624. Do Qiagen RNeasy spin columns expire? - (reply: 1)
625. pcr purification - (reply: 1)
626. E. coli strain for conjugation - (reply: 1)
627. Incorporating RNAse A into DNA extraction - (reply: 2)
628. How to clone insert with one sticky and one blunt end into vector? - (reply: 1)
629. PCR band moves lower than its size on agarose gel - (reply: 3)
630. DNA-PEI in anionic liposomes, picogreen quantification - (reply: 1)