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301. Question about the RT PCR - (reply: 3)
302. PCR ready mixes with long shelf lives - (reply: 4)
303. Problem with repeatability of the standard curve - (reply: 3)
304. Influenza virus - (reply: 3)
305. Defining standards in qPCR softwares - (reply: 3)
306. How to design primer to amplify genomic DNA? - (reply: 3)
307. Overlap PCR, need help - (reply: 11)
308. Internal control for miRNA RT-PCR - (reply: 1)
309. Primers - (reply: 1)
310. Primers mix - (reply: 2)
311. degenerate bases in my sequences - (reply: 1)
312. Need help with dCAPS pcr, seeing huge bands on gel - (reply: 1)
313. How do I make GTE buffer for alkaline lysis? - (reply: 2)
314. Having problem with primers for qPCR - (reply: 4)
315. strange raw data - - (reply: 3)
316. need a method for oligonucleotide visualization - (reply: 5)
317. Bad fragment amplification - (reply: 4)
318. problem with ChiP q-PCR - (reply: 4)
319. suitable single-copy gene target for fungal qPCR - (reply: 4)
320. Increasing specificity of allele-specific Tq probes? - (reply: 2)
321. No amplification with TRAPEZE kit! - (reply: 1)
322. qPCR of Intronless gene - (reply: 4)
323. cDNA not enough-variability - (reply: 2)
324. Stargazer PCR problems - (reply: 3)
325. General PCR discussion - (reply: 8)
326. User error or pipette contamination - (reply: 3)
327. Reverse transcription 101 question! - (reply: 5)
328. Real time PCR doubt - (reply: 5)
329. High Ct values in ref gene as well as target gene - (reply: 3)
330. GADPH does not express - (reply: 1)
302. PCR ready mixes with long shelf lives - (reply: 4)
303. Problem with repeatability of the standard curve - (reply: 3)
304. Influenza virus - (reply: 3)
305. Defining standards in qPCR softwares - (reply: 3)
306. How to design primer to amplify genomic DNA? - (reply: 3)
307. Overlap PCR, need help - (reply: 11)
308. Internal control for miRNA RT-PCR - (reply: 1)
309. Primers - (reply: 1)
310. Primers mix - (reply: 2)
311. degenerate bases in my sequences - (reply: 1)
312. Need help with dCAPS pcr, seeing huge bands on gel - (reply: 1)
313. How do I make GTE buffer for alkaline lysis? - (reply: 2)
314. Having problem with primers for qPCR - (reply: 4)
315. strange raw data - - (reply: 3)
316. need a method for oligonucleotide visualization - (reply: 5)
317. Bad fragment amplification - (reply: 4)
318. problem with ChiP q-PCR - (reply: 4)
319. suitable single-copy gene target for fungal qPCR - (reply: 4)
320. Increasing specificity of allele-specific Tq probes? - (reply: 2)
321. No amplification with TRAPEZE kit! - (reply: 1)
322. qPCR of Intronless gene - (reply: 4)
323. cDNA not enough-variability - (reply: 2)
324. Stargazer PCR problems - (reply: 3)
325. General PCR discussion - (reply: 8)
326. User error or pipette contamination - (reply: 3)
327. Reverse transcription 101 question! - (reply: 5)
328. Real time PCR doubt - (reply: 5)
329. High Ct values in ref gene as well as target gene - (reply: 3)
330. GADPH does not express - (reply: 1)