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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
481. Tm variation - (reply: 1)
482. PCR with more than one primer - (reply: 1)
483. RAPD - PCR problem - (reply: 5)
484. Relative fold expression and Normalization fold expression - (reply: 2)
485. Strange Bands - (reply: 2)
486. Recommended tamplate DNA concentration for qPCR - (reply: 2)
487. RT / cDNA synthesis - (reply: 7)
488. How to best store PCR product? - (reply: 2)
489. smearing below band of interest - (reply: 5)
490. RT-PCR primer design - (reply: 1)
491. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
492. Odd gel run following PCR - (reply: 28)
493. Qiagen PCR Array Reagents? - (reply: 1)
494. Enough checks for gDNA contamination in qPCR? - (reply: 3)
495. plate stuck in ABI7300 - (reply: 7)
496. No or very weak band using 16s primers - (reply: 1)
497. No PCR amplification with b-actin primers - (reply: 1)
498. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
499. optical qPCR plates - (reply: 1)
500. Fold change significance - (reply: 2)
501. No PCR amplified with long primers - (reply: 10)
502. How many real time-PCR reactions for statistics and how? - (reply: 4)
503. PCR optimization: PCR vs qPCR - (reply: 4)
504. PCR smear for genomic samples - (reply: 4)
505. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
506. Saliva and GCF DNA purification - (reply: 1)
507. rtPCR working but the elongated product wont gel! - (reply: 1)
508. another primer dilution question - (reply: 2)
509. TaqMan qPCR low-template issues - (reply: 1)
510. qPCR standard curve slope (m) - (reply: 2)