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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
451. Strange Bands - (reply: 2)
452. Recommended tamplate DNA concentration for qPCR - (reply: 2)
453. RT / cDNA synthesis - (reply: 7)
454. How to best store PCR product? - (reply: 2)
455. smearing below band of interest - (reply: 5)
456. RT-PCR primer design - (reply: 1)
457. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
458. Odd gel run following PCR - (reply: 28)
459. Qiagen PCR Array Reagents? - (reply: 1)
460. Enough checks for gDNA contamination in qPCR? - (reply: 3)
461. plate stuck in ABI7300 - (reply: 7)
462. No or very weak band using 16s primers - (reply: 1)
463. No PCR amplification with b-actin primers - (reply: 1)
464. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
465. optical qPCR plates - (reply: 1)
466. Fold change significance - (reply: 2)
467. No PCR amplified with long primers - (reply: 10)
468. How many real time-PCR reactions for statistics and how? - (reply: 4)
469. PCR optimization: PCR vs qPCR - (reply: 4)
470. PCR smear for genomic samples - (reply: 4)
471. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
472. Saliva and GCF DNA purification - (reply: 1)
473. rtPCR working but the elongated product wont gel! - (reply: 1)
474. another primer dilution question - (reply: 2)
475. TaqMan qPCR low-template issues - (reply: 1)
476. qPCR standard curve slope (m) - (reply: 2)
477. 16s double bands obtained-why?? - (reply: 2)
478. Application of RNase - (reply: 3)
479. i need help with virus pcr - (reply: 2)
480. Primer Efficiency - (reply: 2)