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Top : New Forum Archives (2009-): : Molecular-Biology
2611. PFGE gel - Can I reuse pulsed field certified gel for PFGE? (reply: 2)
2612. Validating real time pcr primers - (reply: 2)
2613. How to find catalytic domain using cDNA - (reply: 2)
2614. low plasmid yield from midi preps - (reply: 4)
2615. Measure nucleotides - (reply: 3)
2616. Proteinase K Protection Assay Conditions - (reply: 2)
2617. no 18S band on RNA agarose gel - (reply: 1)
2618. b-mercaptoethanol in lysis buffer - (reply: 1)
2619. Serum Batch Test.... - What to do?? (reply: 3)
2620. what is the activity of TAQ at 60 centigrade? - (reply: 2)
2621. Could You Suggest me A good KIt for DNA extraction from Yeast? - (reply: 1)
2622. DNA extraction trouble - (reply: 7)
2623. Good RT-PCR amplication but NO amplification with semi-quantitative PCR!? Wh - (reply: 3)
2624. gel extraction protocol for small amount of starting material - (reply: 3)
2625. Taq introduces error after? - (reply: 4)
2626. nylon membranes bleaching - (reply: 2)
2627. DNA vs Protein Stains - Are there any that don't stain BOTH? (reply: 1)
2628. Plasmid isolation, help with dilution step? - (reply: 7)
2629. Extraction of large size genomic DNA - (reply: 3)
2630. full digestion of plasmid to get only dNTPs - (reply: 3)
2631. Incorporate biotinylated-dNTPs by a polymerase - biotin (reply: 1)
2632. multiple bands in my RNA sample? - (reply: 2)
2633. expession only in +ve controls - (reply: 4)
2634. splice variant encoding same protein - (reply: 1)
2635. EtBr contamination risk - safety question (reply: 4)
2636. WHich primer to use for sequencing - (reply: 5)
2637. types of gel stains - (reply: 7)
2638. minimum length for the gene to be amplified in PCR - (reply: 6)
2639. wrong gene - (reply: 13)
2640. pheno chloroform step - (reply: 6)