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Top : New Forum Archives (2009-): : Molecular-Biology
2521. PROTEIN PRECIPITATION SOLUTION - (reply: 1)
2522. cloning - How to calculate the insert and linear plsmid concentration for ligati (reply: 1)
2523. PFGE gel - Can I reuse pulsed field certified gel for PFGE? (reply: 2)
2524. Validating real time pcr primers - (reply: 2)
2525. How to find catalytic domain using cDNA - (reply: 2)
2526. low plasmid yield from midi preps - (reply: 4)
2527. Measure nucleotides - (reply: 3)
2528. Proteinase K Protection Assay Conditions - (reply: 2)
2529. no 18S band on RNA agarose gel - (reply: 1)
2530. b-mercaptoethanol in lysis buffer - (reply: 1)
2531. Serum Batch Test.... - What to do?? (reply: 3)
2532. what is the activity of TAQ at 60 centigrade? - (reply: 2)
2533. Could You Suggest me A good KIt for DNA extraction from Yeast? - (reply: 1)
2534. DNA extraction trouble - (reply: 7)
2535. Good RT-PCR amplication but NO amplification with semi-quantitative PCR!? Wh - (reply: 3)
2536. gel extraction protocol for small amount of starting material - (reply: 3)
2537. Taq introduces error after? - (reply: 4)
2538. nylon membranes bleaching - (reply: 2)
2539. DNA vs Protein Stains - Are there any that don't stain BOTH? (reply: 1)
2540. Plasmid isolation, help with dilution step? - (reply: 7)
2541. Extraction of large size genomic DNA - (reply: 3)
2542. full digestion of plasmid to get only dNTPs - (reply: 3)
2543. Incorporate biotinylated-dNTPs by a polymerase - biotin (reply: 1)
2544. multiple bands in my RNA sample? - (reply: 2)
2545. expession only in +ve controls - (reply: 4)
2546. splice variant encoding same protein - (reply: 1)
2547. EtBr contamination risk - safety question (reply: 4)
2548. WHich primer to use for sequencing - (reply: 5)
2549. types of gel stains - (reply: 7)
2550. minimum length for the gene to be amplified in PCR - (reply: 6)