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Top : New Forum Archives (2009-): : Molecular-Biology
2791. mutations in plasmids - (reply: 3)
2792. reporter assay with ligand activated TF - (reply: 8)
2793. synthetic scfv - (reply: 2)
2794. get rid of RNA from Maxi - (reply: 1)
2795. Tips for genomic DNA extraction from gram -ve bacteria - (reply: 2)
2796. Primers Not working - Real time PCR using SYBR Green (reply: 3)
2797. PCR conditions with three primers - (reply: 1)
2798. RNA labeling - (reply: 3)
2799. Immunoprecipitation - Multiple proteins from single lysate (reply: 2)
2800. about real time qPCR - (reply: 1)
2801. Mutation - Δ/Δ (reply: 4)
2802. Cloning a labeled PCR product - (reply: 1)
2803. where to get T4 phages - (reply: 3)
2804. Best method to concentrate RNA/cDNA? - (reply: 5)
2805. in situ probe design - (reply: 1)
2806. miniprep and maxiprep - (reply: 9)
2807. DNA extraction methods - PCI extrction (reply: 3)
2808. RNA electrophoresis - (reply: 3)
2809. Plant DNA extraction - (reply: 5)
2810. PCR and cloning - (reply: 14)
2811. restriction enzyme based on forward or reverse sequence - restriction enzyme based on forward or reverse sequence (reply: 2)
2812. PCR product - not suppose to be there (reply: 7)
2813. Big insert to put back into the vector - (reply: 17)
2814. Seperate DNA spin columns - (reply: 3)
2815. the product length should be 306bp - the product length should be 306bp (reply: 4)
2816. plasmid spin column usage - (reply: 5)
2817. dominat negative mutants - (reply: 3)
2818. RNA Extraction & EMSA - (reply: 1)
2819. electroporation of HL60 cells - (reply: 1)
2820. Digest genomic (eukaryote) DNA before running PCR, is it necessary? - I do not get any band from PCR using genomic DNA and different primers (reply: 6)