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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1171. Conventional PCR problems - wisamni2004 (reply: 2)
1172. Questions of Standards making in relative qRT-PCR - (reply: 2)
1173. relative comparison of many samples and genes in qRT-PCR - (reply: 1)
1174. NTC & Negtive control - (reply: 2)
1175. Is it possible to know only the live bacteria using PCR for a certain genus? - (reply: 1)
1176. incorrect/smaller band size for real time PCR - (reply: 1)
1177. Reference genes and dilutions in qPCR - (reply: 1)
1178. Issue with standard curve for qPCR for CHiP - (reply: 1)
1179. Northern - Do not get Bands in Northern Blot (reply: 2)
1180. qPCR data analysis - (reply: 1)
1181. Copy number of normalizer gene - real time normalization (reply: 1)
1182. assistance with PCR amplification please - (reply: 3)
1183. Mutagenesis not working - (reply: 5)
1184. I need an urgent help with q-pcr amplification plots - (reply: 11)
1185. Primers - Primers (reply: 2)
1186. Problems with the Specificity of the Primers - (reply: 2)
1187. qPCR Data analysis - qBasePlus and GenEx (reply: 1)
1188. confusion in real time PCR primers - Confusion in Real time pcr primers (reply: 3)
1189. Degenerate primers PCR problem, Please help! - (reply: 2)
1190. degenerated Taqman probes? - (reply: 1)
1191. error message on qPCR mashine - (reply: 1)
1192. Hotstart PCR and unspecific Amplification - (reply: 3)
1193. Primer design help needed - (reply: 1)
1194. Primers no longer work - (reply: 1)
1195. Sequencing - why are left-over PCR primers an issue? - (reply: 3)
1196. Primer Design with Primer-Blast - My experience has been worse than just using Primer3 and BLAT separate (reply: 4)
1197. colony PCR - (reply: 2)
1198. copy number variation - (reply: 3)
1199. How to deal with truncated mRNA or mRNA that has secondary structure - (reply: 2)
1200. Very weird gel - I cannot explain these results (reply: 11)