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Top : New Forum Archives (2009-): : Molecular-Biology
2521. DNA extraction trouble - (reply: 7)
2522. Good RT-PCR amplication but NO amplification with semi-quantitative PCR!? Wh - (reply: 3)
2523. gel extraction protocol for small amount of starting material - (reply: 3)
2524. Taq introduces error after? - (reply: 4)
2525. nylon membranes bleaching - (reply: 2)
2526. DNA vs Protein Stains - Are there any that don't stain BOTH? (reply: 1)
2527. Plasmid isolation, help with dilution step? - (reply: 7)
2528. Extraction of large size genomic DNA - (reply: 3)
2529. full digestion of plasmid to get only dNTPs - (reply: 3)
2530. Incorporate biotinylated-dNTPs by a polymerase - biotin (reply: 1)
2531. multiple bands in my RNA sample? - (reply: 2)
2532. expession only in +ve controls - (reply: 4)
2533. splice variant encoding same protein - (reply: 1)
2534. EtBr contamination risk - safety question (reply: 4)
2535. WHich primer to use for sequencing - (reply: 5)
2536. types of gel stains - (reply: 7)
2537. minimum length for the gene to be amplified in PCR - (reply: 6)
2538. wrong gene - (reply: 13)
2539. pheno chloroform step - (reply: 6)
2540. dNTP Quantity - (reply: 3)
2541. gene design - restriction site addition (reply: 2)
2542. 5' RACE products appearance on 1.5% agarose gel - (reply: 8)
2543. DNA Question for TV Show - (reply: 4)
2544. Amplification dwindles using little template RT-PCR - (reply: 3)
2545. Phenol chloroform extraction of DNA - (reply: 3)
2546. Number of genes and number of proteins in humans - (reply: 1)
2547. Degenerate PCR Size Limit? - (reply: 3)
2548. RNA isolation form plants - (reply: 4)
2549. 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)
2550. 5' end RNA biotin labeling - need protocol (reply: 2)