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511. Two reverse primer sequences for a single forward primer - (reply: 1)
512. Tm variation - (reply: 1)
513. PCR with more than one primer - (reply: 1)
514. RAPD - PCR problem - (reply: 5)
515. Relative fold expression and Normalization fold expression - (reply: 2)
516. Strange Bands - (reply: 2)
517. Recommended tamplate DNA concentration for qPCR - (reply: 2)
518. RT / cDNA synthesis - (reply: 7)
519. How to best store PCR product? - (reply: 2)
520. smearing below band of interest - (reply: 5)
521. RT-PCR primer design - (reply: 1)
522. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
523. Odd gel run following PCR - (reply: 28)
524. Qiagen PCR Array Reagents? - (reply: 1)
525. Enough checks for gDNA contamination in qPCR? - (reply: 3)
526. plate stuck in ABI7300 - (reply: 7)
527. No or very weak band using 16s primers - (reply: 1)
528. No PCR amplification with b-actin primers - (reply: 1)
529. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
530. optical qPCR plates - (reply: 1)
531. Fold change significance - (reply: 2)
532. No PCR amplified with long primers - (reply: 10)
533. How many real time-PCR reactions for statistics and how? - (reply: 4)
534. PCR optimization: PCR vs qPCR - (reply: 4)
535. PCR smear for genomic samples - (reply: 4)
536. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
537. Saliva and GCF DNA purification - (reply: 1)
538. rtPCR working but the elongated product wont gel! - (reply: 1)
539. another primer dilution question - (reply: 2)
540. TaqMan qPCR low-template issues - (reply: 1)
512. Tm variation - (reply: 1)
513. PCR with more than one primer - (reply: 1)
514. RAPD - PCR problem - (reply: 5)
515. Relative fold expression and Normalization fold expression - (reply: 2)
516. Strange Bands - (reply: 2)
517. Recommended tamplate DNA concentration for qPCR - (reply: 2)
518. RT / cDNA synthesis - (reply: 7)
519. How to best store PCR product? - (reply: 2)
520. smearing below band of interest - (reply: 5)
521. RT-PCR primer design - (reply: 1)
522. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
523. Odd gel run following PCR - (reply: 28)
524. Qiagen PCR Array Reagents? - (reply: 1)
525. Enough checks for gDNA contamination in qPCR? - (reply: 3)
526. plate stuck in ABI7300 - (reply: 7)
527. No or very weak band using 16s primers - (reply: 1)
528. No PCR amplification with b-actin primers - (reply: 1)
529. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
530. optical qPCR plates - (reply: 1)
531. Fold change significance - (reply: 2)
532. No PCR amplified with long primers - (reply: 10)
533. How many real time-PCR reactions for statistics and how? - (reply: 4)
534. PCR optimization: PCR vs qPCR - (reply: 4)
535. PCR smear for genomic samples - (reply: 4)
536. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
537. Saliva and GCF DNA purification - (reply: 1)
538. rtPCR working but the elongated product wont gel! - (reply: 1)
539. another primer dilution question - (reply: 2)
540. TaqMan qPCR low-template issues - (reply: 1)