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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
421. UNG in PCR - (reply: 1)
422. Cause of random samples failing PCR? - (reply: 2)
423. Template DNA for PCR- Concrentration or Volume?? - (reply: 1)
424. RNA extraction - (reply: 3)
425. Normalization of Ct of interest to a reference Ct - (reply: 3)
426. urgent: need help with qPCR statistics - (reply: 2)
427. A question for Reverse transcription experts - (reply: 5)
428. will mRNA from different cell line lead to loss of expected product in RT PCR? - (reply: 2)
429. PCR amplification with new restriction sites troubleshooting - (reply: 2)
430. using cell line to generate standard curve - (reply: 6)
431. PCR DNA Concentration - (reply: 1)
432. 3' RACE creates too big band doesn't leave well - (reply: 1)
433. RT-PCR product- no band - (reply: 4)
434. Normalization factor - (reply: 3)
435. Understanding RACE PCR - (reply: 1)
436. SYBR Select Master Mix for CFX from Invitrogen - Storage - (reply: 4)
437. Dye for qPCR - (reply: 3)
438. Pair of primers (SYBR) with more than one amplicon product(?) - (reply: 4)
439. Wierd Bands after PCR....Confused - (reply: 9)
440. PCR with Plasmid recovered from filter paper - (reply: 6)
441. PCR amplified product size - (reply: 5)
442. Opinion: What fold change is actually considered meaningful - (reply: 2)
443. Buffers RNase decontamination - (reply: 1)
444. the storage time for primers - (reply: 9)
445. Annealing temperature for PCR - (reply: 8)
446. can canine COL1A1 primers be used to quantify human COL1A1 cDNA in qPCR - (reply: 1)
447. Nested PCR - (reply: 2)
448. random primers or oligodT - (reply: 4)
449. Confused about normalization - (reply: 2)
450. To design or use published primers? - (reply: 4)