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Top : New Forum Archives (2009-): : Molecular-Biology
2581. Could You Suggest me A good KIt for DNA extraction from Yeast? - (reply: 1)
2582. DNA extraction trouble - (reply: 7)
2583. Good RT-PCR amplication but NO amplification with semi-quantitative PCR!? Wh - (reply: 3)
2584. gel extraction protocol for small amount of starting material - (reply: 3)
2585. Taq introduces error after? - (reply: 4)
2586. nylon membranes bleaching - (reply: 2)
2587. DNA vs Protein Stains - Are there any that don't stain BOTH? (reply: 1)
2588. Plasmid isolation, help with dilution step? - (reply: 7)
2589. Extraction of large size genomic DNA - (reply: 3)
2590. full digestion of plasmid to get only dNTPs - (reply: 3)
2591. Incorporate biotinylated-dNTPs by a polymerase - biotin (reply: 1)
2592. multiple bands in my RNA sample? - (reply: 2)
2593. expession only in +ve controls - (reply: 4)
2594. splice variant encoding same protein - (reply: 1)
2595. EtBr contamination risk - safety question (reply: 4)
2596. WHich primer to use for sequencing - (reply: 5)
2597. types of gel stains - (reply: 7)
2598. minimum length for the gene to be amplified in PCR - (reply: 6)
2599. wrong gene - (reply: 13)
2600. pheno chloroform step - (reply: 6)
2601. dNTP Quantity - (reply: 3)
2602. gene design - restriction site addition (reply: 2)
2603. 5' RACE products appearance on 1.5% agarose gel - (reply: 8)
2604. DNA Question for TV Show - (reply: 4)
2605. Amplification dwindles using little template RT-PCR - (reply: 3)
2606. Phenol chloroform extraction of DNA - (reply: 3)
2607. Number of genes and number of proteins in humans - (reply: 1)
2608. Degenerate PCR Size Limit? - (reply: 3)
2609. RNA isolation form plants - (reply: 4)
2610. How to increase the concentration insert or vector or no cut plasmid - How to increase the concentration insert or vector or no cut plasmid (reply: 4)