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Top : New Forum Archives (2009-): : Molecular-Biology
151. Troubleshooting with cloning - (reply: 2)
152. qPCR acceptable standard deviation - (reply: 1)
153. Gel doubling banding and resolution problem - (reply: 6)
154. Canīt get rid of DNA contamination in RNA - (reply: 2)
155. PCR DNA bands too large on agarose gel - (reply: 1)
156. Easy to transfect primary cell line? - (reply: 1)
157. Sequence specific pulldown of dsDNA - (reply: 8)
158. Gene expression and transcription factors - (reply: 1)
159. RNA gel problem (melted bands) - (reply: 2)
160. RNA extraction and DNase treatment - (reply: 1)
161. Cloning purified PCR product into cells - (reply: 5)
162. Mention of Transgene Insertion into Cell Lines By Transfecting with cDNA - (reply: 2)
163. when to add polybrene for lentivirus transduction? - (reply: 1)
164. How to know the plasmid extracted are indeed the plasmid of interest? - (reply: 4)
165. In situ hybridization - (reply: 5)
166. Sypro Ruby Dye Front - (reply: 9)
167. Forced Expression vs. Enforced Expression - (reply: 1)
168. Co-immunoprecipitation non-specific binding - (reply: 2)
169. New webpage and software tools - (reply: 1)
170. What DCH5a cells are? / pCAMBIA1301 isolation from DHC5a cells - (reply: 3)
171. Can I snap freeze my tissue (liquid nitrogen) in Lysis buffer for later RNA extr - (reply: 6)
172. Gateway cloning not working. - (reply: 7)
173. Assays from very few number of cells - (reply: 1)
174. EM7 promoter - what is it? - (reply: 1)
175. Virus processing (filtration) of blood - How to? - (reply: 5)
176. ABC(D) Model of Plant Flowers - (reply: 1)
177. TE buffer pH adjustment - (reply: 1)
178. Estimate cost for Molecular Docking software/devices - (reply: 1)
179. Polymorphism - (reply: 2)
180. PCR_QUALITY CONTROL - (reply: 2)