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Top : New Forum Archives (2009-): : SDS-PAGE-and-Western-Blotting
871. Not sure of what % to use for gels - (reply: 6)
872. Protein Size - (reply: 3)
873. no separation of MW marker on gel - (reply: 1)
874. Transfer basic protein to PVDF - (reply: 1)
875. Expired pre-cast gels - (reply: 4)
876. LDS sample buffer in 95C - (reply: 2)
877. disappearing high molecular protein and marker,thanks - (reply: 1)
878. Use of cold milk??? - Western blot (reply: 2)
879. Antibody compatibility between different species - (reply: 4)
880. "weber & osborne" and neville's SDS-PAGE method - protocol please (reply: 6)
881. Wrong bands on the blot - (reply: 4)
882. Protein drag in IEF-WB - (reply: 3)
883. SDS-PAGE gel staining problem - (reply: 1)
884. sample buffer pH - its effect?? (reply: 12)
885. SDS-Page and DMSO - (reply: 2)
886. Help with Western Blotting of Keratin Proteins - (reply: 2)
887. Problems detecting my band! - (reply: 2)
888. How many times can I reuse Ponceau S? - (reply: 3)
889. sds-page problems - polymerization of acrylamide (reply: 5)
890. western blot w/ anti-FLAG ab - multiple bands show up (reply: 7)
891. what is the glycine for in running and trans buffer? - and what is the Tris for? (reply: 1)
892. Why do I always get these ugly bands? - I always end up with some fused and tandemed bands... (reply: 7)
893. Interpreting a gel - (reply: 3)
894. Plant isoenzymes! - (reply: 7)
895. cytochrome C Western Blot - (reply: 7)
896. Protein size and gel percentage - (reply: 7)
897. Bands visible in membrane but not in the film - ?? (reply: 10)
898. non desired brigther bands - (reply: 7)
899. Dimer or monomer - (reply: 11)
900. Protein precipitation by TCA acid + acetone - (reply: 4)

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