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