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Top : New Forum Archives (2009-): : Molecular-Biology
2581. Validating real time pcr primers - (reply: 2)
2582. How to find catalytic domain using cDNA - (reply: 2)
2583. low plasmid yield from midi preps - (reply: 4)
2584. Measure nucleotides - (reply: 3)
2585. Proteinase K Protection Assay Conditions - (reply: 2)
2586. no 18S band on RNA agarose gel - (reply: 1)
2587. b-mercaptoethanol in lysis buffer - (reply: 1)
2588. Serum Batch Test.... - What to do?? (reply: 3)
2589. what is the activity of TAQ at 60 centigrade? - (reply: 2)
2590. Could You Suggest me A good KIt for DNA extraction from Yeast? - (reply: 1)
2591. DNA extraction trouble - (reply: 7)
2592. Good RT-PCR amplication but NO amplification with semi-quantitative PCR!? Wh - (reply: 3)
2593. gel extraction protocol for small amount of starting material - (reply: 3)
2594. Taq introduces error after? - (reply: 4)
2595. nylon membranes bleaching - (reply: 2)
2596. DNA vs Protein Stains - Are there any that don't stain BOTH? (reply: 1)
2597. Plasmid isolation, help with dilution step? - (reply: 7)
2598. Extraction of large size genomic DNA - (reply: 3)
2599. full digestion of plasmid to get only dNTPs - (reply: 3)
2600. Incorporate biotinylated-dNTPs by a polymerase - biotin (reply: 1)
2601. multiple bands in my RNA sample? - (reply: 2)
2602. expession only in +ve controls - (reply: 4)
2603. splice variant encoding same protein - (reply: 1)
2604. EtBr contamination risk - safety question (reply: 4)
2605. WHich primer to use for sequencing - (reply: 5)
2606. types of gel stains - (reply: 7)
2607. minimum length for the gene to be amplified in PCR - (reply: 6)
2608. wrong gene - (reply: 13)
2609. pheno chloroform step - (reply: 6)
2610. dNTP Quantity - (reply: 3)