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Top : New Forum Archives (2009-): : Molecular-Biology
2611. Good RT-PCR amplication but NO amplification with semi-quantitative PCR!? Wh - (reply: 3)
2612. gel extraction protocol for small amount of starting material - (reply: 3)
2613. Taq introduces error after? - (reply: 4)
2614. nylon membranes bleaching - (reply: 2)
2615. DNA vs Protein Stains - Are there any that don't stain BOTH? (reply: 1)
2616. Plasmid isolation, help with dilution step? - (reply: 7)
2617. Extraction of large size genomic DNA - (reply: 3)
2618. full digestion of plasmid to get only dNTPs - (reply: 3)
2619. Incorporate biotinylated-dNTPs by a polymerase - biotin (reply: 1)
2620. multiple bands in my RNA sample? - (reply: 2)
2621. expession only in +ve controls - (reply: 4)
2622. splice variant encoding same protein - (reply: 1)
2623. EtBr contamination risk - safety question (reply: 4)
2624. WHich primer to use for sequencing - (reply: 5)
2625. types of gel stains - (reply: 7)
2626. minimum length for the gene to be amplified in PCR - (reply: 6)
2627. wrong gene - (reply: 13)
2628. pheno chloroform step - (reply: 6)
2629. dNTP Quantity - (reply: 3)
2630. gene design - restriction site addition (reply: 2)
2631. 5' RACE products appearance on 1.5% agarose gel - (reply: 8)
2632. DNA Question for TV Show - (reply: 4)
2633. Amplification dwindles using little template RT-PCR - (reply: 3)
2634. Phenol chloroform extraction of DNA - (reply: 3)
2635. Number of genes and number of proteins in humans - (reply: 1)
2636. Degenerate PCR Size Limit? - (reply: 3)
2637. RNA isolation form plants - (reply: 4)
2638. 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)
2639. 5' end RNA biotin labeling - need protocol (reply: 2)
2640. Yeast complementation test - (reply: 1)