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New Forum Archives (2009-): :
481. PCR amplification of large template - (reply: 1)
483. Doubt: genomic dna library construction - (reply: 3)
485. Strange Negative Contamination Issue. - (reply: 2)
487. How to quantify MS2 virus-like particles? - (reply: 1)
489. Blue middle tint in white colonies for Blue/White screening - (reply: 2)
491. No DNA after gel extraction - (reply: 9)
493. DNA isolation from nuclei - (reply: 5)
495. Why do people typically use AP instead of HRP for Southerns? - (reply: 2)
497. Low Transformation Efficiency with a Specific Gene - (reply: 4)
499. Problems with plasmid DNA extraction - (reply: 3)
501. What part of the promoter to clone - (reply: 2)
503. Biotinylated RNA on Nylon Membrane - (reply: 2)
505. UV crosslinkers, changing UV bulbs? - (reply: 1)
507. Weird gel banding for apoptosis - (reply: 3)
509. Co-IP vs Pull down - (reply: 2)
483. Doubt: genomic dna library construction - (reply: 3)
485. Strange Negative Contamination Issue. - (reply: 2)
487. How to quantify MS2 virus-like particles? - (reply: 1)
489. Blue middle tint in white colonies for Blue/White screening - (reply: 2)
491. No DNA after gel extraction - (reply: 9)
493. DNA isolation from nuclei - (reply: 5)
495. Why do people typically use AP instead of HRP for Southerns? - (reply: 2)
497. Low Transformation Efficiency with a Specific Gene - (reply: 4)
499. Problems with plasmid DNA extraction - (reply: 3)
501. What part of the promoter to clone - (reply: 2)
503. Biotinylated RNA on Nylon Membrane - (reply: 2)
505. UV crosslinkers, changing UV bulbs? - (reply: 1)
507. Weird gel banding for apoptosis - (reply: 3)
509. Co-IP vs Pull down - (reply: 2)