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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1141. Conventional PCR problems - wisamni2004 (reply: 2)
1142. Questions of Standards making in relative qRT-PCR - (reply: 2)
1143. relative comparison of many samples and genes in qRT-PCR - (reply: 1)
1144. NTC & Negtive control - (reply: 2)
1145. Is it possible to know only the live bacteria using PCR for a certain genus? - (reply: 1)
1146. incorrect/smaller band size for real time PCR - (reply: 1)
1147. Reference genes and dilutions in qPCR - (reply: 1)
1148. Issue with standard curve for qPCR for CHiP - (reply: 1)
1149. Northern - Do not get Bands in Northern Blot (reply: 2)
1150. qPCR data analysis - (reply: 1)
1151. Copy number of normalizer gene - real time normalization (reply: 1)
1152. assistance with PCR amplification please - (reply: 3)
1153. Mutagenesis not working - (reply: 5)
1154. I need an urgent help with q-pcr amplification plots - (reply: 11)
1155. Primers - Primers (reply: 2)
1156. Problems with the Specificity of the Primers - (reply: 2)
1157. qPCR Data analysis - qBasePlus and GenEx (reply: 1)
1158. confusion in real time PCR primers - Confusion in Real time pcr primers (reply: 3)
1159. Degenerate primers PCR problem, Please help! - (reply: 2)
1160. degenerated Taqman probes? - (reply: 1)
1161. error message on qPCR mashine - (reply: 1)
1162. Hotstart PCR and unspecific Amplification - (reply: 3)
1163. Primer design help needed - (reply: 1)
1164. Primers no longer work - (reply: 1)
1165. Sequencing - why are left-over PCR primers an issue? - (reply: 3)
1166. Primer Design with Primer-Blast - My experience has been worse than just using Primer3 and BLAT separate (reply: 4)
1167. colony PCR - (reply: 2)
1168. copy number variation - (reply: 3)
1169. How to deal with truncated mRNA or mRNA that has secondary structure - (reply: 2)
1170. Very weird gel - I cannot explain these results (reply: 11)