Protocol Online logo
Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
151. Missing DNA Target and Effect on Non-Specific Amplicons - (reply: 1)
152. 3 RACE-PCR of cDNA ends yielded a piece of 2 different genes? - (reply: 2)
153. how to make this reaction? - (reply: 1)
154. What is the difference between Hot start polymerase and the taq polymerase - (reply: 3)
155. How long can I store at - 30C my PCR mix? - (reply: 6)
156. How to set up real-time PCR for yes/no bands (rearrangement) - (reply: 4)
157. RNA concentration is too low to detect gene of interest by qRT-PCR - (reply: 4)
158. RT-PCR help - (reply: 2)
159. Strange signals in the NTC - (reply: 1)
160. False positive - help - (reply: 3)
161. Autoclaving PCR waste in the room where PCRs are set up and run - Is it a proble - (reply: 2)
162. PCR Temperature change control malfunctioning - (reply: 1)
163. Assay question - (reply: 1)
164. WHY NO ONE REPLIES, is this a stupid question ? - (reply: 5)
165. HRM instrumentaion - (reply: 4)
166. Can you repeat a thermocycle? - (reply: 3)
167. Any online tool to check the propability of primer dimer formetion _ - (reply: 4)
168. Amplification curve in the negative control samples - (reply: 7)
169. PCR troubleshooting: wrong amplicon size when spiked into sample - (reply: 4)
170. Primer as limiting reagent in PCR reaction - (reply: 2)
171. Taqman probe in a LightCycler 480? - (reply: 1)
172. Real time PCR for degraded RNA - (reply: 1)
173. Ct value of housekeeping gene - (reply: 4)
174. Efficiency correct fold change -- use all or none? - (reply: 1)
175. Microfluidic PCR Issues, Master Mix and Consumable Variations? - (reply: 5)
176. Doubled polymerase in the rxn, does this increase pcr efficiency? - (reply: 1)
177. If I am running Real-Time PCR with one gene of interest and one reference gene(G - (reply: 4)
178. Do I need to run HKG together with the GOI everytime I run Real-Time PCR? - (reply: 1)
179. Is this primer-dimer peak in my melting curve? - (reply: 6)
180. Taq / Phusion mix - (reply: 3)