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Top : New Forum Archives (2009-): : SDS-PAGE-and-Western-Blotting
871. PBS in my Tris Glycine Running Buffer....what will happen - (reply: 3)
872. Secondary Antibody reacting with Loading Buffer? Is this possible? - Having problems with unidentified bands in western blot (reply: 3)
873. how to get rabbit antibody for Western blotting - (reply: 2)
874. voltage/amper problem in western blot - Is there a link between volts (or mAm)and resolution? (reply: 1)
875. Not sure of what % to use for gels - (reply: 6)
876. Protein Size - (reply: 3)
877. no separation of MW marker on gel - (reply: 1)
878. Transfer basic protein to PVDF - (reply: 1)
879. Expired pre-cast gels - (reply: 4)
880. LDS sample buffer in 95C - (reply: 2)
881. disappearing high molecular protein and marker,thanks - (reply: 1)
882. Use of cold milk??? - Western blot (reply: 2)
883. Antibody compatibility between different species - (reply: 4)
884. "weber & osborne" and neville's SDS-PAGE method - protocol please (reply: 6)
885. Wrong bands on the blot - (reply: 4)
886. Protein drag in IEF-WB - (reply: 3)
887. SDS-PAGE gel staining problem - (reply: 1)
888. sample buffer pH - its effect?? (reply: 12)
889. SDS-Page and DMSO - (reply: 2)
890. Help with Western Blotting of Keratin Proteins - (reply: 2)
891. Problems detecting my band! - (reply: 2)
892. How many times can I reuse Ponceau S? - (reply: 3)
893. sds-page problems - polymerization of acrylamide (reply: 5)
894. western blot w/ anti-FLAG ab - multiple bands show up (reply: 7)
895. what is the glycine for in running and trans buffer? - and what is the Tris for? (reply: 1)
896. Why do I always get these ugly bands? - I always end up with some fused and tandemed bands... (reply: 7)
897. Interpreting a gel - (reply: 3)
898. Plant isoenzymes! - (reply: 7)
899. cytochrome C Western Blot - (reply: 7)
900. Protein size and gel percentage - (reply: 7)

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