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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
391. Are these primer products good enough for qPCR? - (reply: 3)
392. mtDNA to nDNA Ratio gDNA - qPCR - (reply: 1)
393. Can't get PCR with large overhang primers to work - (reply: 8)
394. Primer Efficiency across runs - (reply: 1)
395. Question about pipet tips for PCR and rtPCR - (reply: 4)
396. Taqman Probe sequence problem - (reply: 4)
397. UNG in PCR - (reply: 1)
398. Cause of random samples failing PCR? - (reply: 2)
399. Template DNA for PCR- Concrentration or Volume?? - (reply: 1)
400. RNA extraction - (reply: 3)
401. Normalization of Ct of interest to a reference Ct - (reply: 3)
402. urgent: need help with qPCR statistics - (reply: 2)
403. A question for Reverse transcription experts - (reply: 5)
404. will mRNA from different cell line lead to loss of expected product in RT PCR? - (reply: 2)
405. PCR amplification with new restriction sites troubleshooting - (reply: 2)
406. using cell line to generate standard curve - (reply: 6)
407. PCR DNA Concentration - (reply: 1)
408. 3' RACE creates too big band doesn't leave well - (reply: 1)
409. RT-PCR product- no band - (reply: 4)
410. Normalization factor - (reply: 3)
411. Understanding RACE PCR - (reply: 1)
412. SYBR Select Master Mix for CFX from Invitrogen - Storage - (reply: 4)
413. Dye for qPCR - (reply: 3)
414. Pair of primers (SYBR) with more than one amplicon product(?) - (reply: 4)
415. Wierd Bands after PCR....Confused - (reply: 9)
416. PCR with Plasmid recovered from filter paper - (reply: 6)
417. PCR amplified product size - (reply: 5)
418. Opinion: What fold change is actually considered meaningful - (reply: 2)
419. Buffers RNase decontamination - (reply: 1)
420. the storage time for primers - (reply: 9)