|
2161. Anyone tried the Qubit? - (reply: 1)
2162. Ethanol precipitation problem ! - (reply: 1)
2163. double digest - trying to isolate a 450bp sequence with no sucess (reply: 6)
2164. When X-gal goes bad - Or, How long should I incubate my plates? (reply: 4)
2165. Colony PCR - (reply: 3)
2166. PLASMA RNA extraction - (reply: 1)
2167. yeast two hybrid problem - (reply: 3)
2168. This sumo sequence correct？ - sumo (reply: 2)
2169. Handling RNA - How to avoid RNase contamination - (reply: 17)
2170. Phenol chloroform ratio during RNA isolation - (reply: 1)
2171. Tris-acetate buffer? - (reply: 4)
2172. genomic dna isolated from blood is brown color?! - (reply: 4)
2173. problem with cloning PCR - can't amply the full-length cDNA with PCR (reply: 6)
2174. labeling dCTP, dATP, dGTP, dTTP - (reply: 2)
2175. Removal of RNA from DNA sample - (reply: 15)
2176. Only DNA ladder , No desired band in PCR - (reply: 4)
2177. taq and PCR - (reply: 6)
2178. Molar concentration of GTC in Ambions Tri Reagant? - Molar concentration of GTC in Ambions Tri Reagant? (reply: 1)
2179. is too much ligation reaction bad for transformation? - (reply: 4)
2180. question about restriction enzyme digest - (reply: 1)
2181. Does purifying PCR probes for EMSA from EtBr gel interfere with binding? - (reply: 1)
2182. RNA gel electrohoresis - (reply: 1)
2183. plasmid dna isolation - (reply: 1)
2184. Two stop codons - (reply: 1)
2185. About antibodies - How resistant are they (reply: 2)
2186. Vector needed - (reply: 1)
2187. Long PCR and genomic DNA isolation problems - (reply: 2)
2188. having the wrong vector in my clone - (reply: 3)
2189. Low Quality Seqeunces - (reply: 3)
2190. could FLAG-tagged protein be used in the Luc assay? - (reply: 1)
2162. Ethanol precipitation problem ! - (reply: 1)
2163. double digest - trying to isolate a 450bp sequence with no sucess (reply: 6)
2164. When X-gal goes bad - Or, How long should I incubate my plates? (reply: 4)
2165. Colony PCR - (reply: 3)
2166. PLASMA RNA extraction - (reply: 1)
2167. yeast two hybrid problem - (reply: 3)
2168. This sumo sequence correct？ - sumo (reply: 2)
2169. Handling RNA - How to avoid RNase contamination - (reply: 17)
2170. Phenol chloroform ratio during RNA isolation - (reply: 1)
2171. Tris-acetate buffer? - (reply: 4)
2172. genomic dna isolated from blood is brown color?! - (reply: 4)
2173. problem with cloning PCR - can't amply the full-length cDNA with PCR (reply: 6)
2174. labeling dCTP, dATP, dGTP, dTTP - (reply: 2)
2175. Removal of RNA from DNA sample - (reply: 15)
2176. Only DNA ladder , No desired band in PCR - (reply: 4)
2177. taq and PCR - (reply: 6)
2178. Molar concentration of GTC in Ambions Tri Reagant? - Molar concentration of GTC in Ambions Tri Reagant? (reply: 1)
2179. is too much ligation reaction bad for transformation? - (reply: 4)
2180. question about restriction enzyme digest - (reply: 1)
2181. Does purifying PCR probes for EMSA from EtBr gel interfere with binding? - (reply: 1)
2182. RNA gel electrohoresis - (reply: 1)
2183. plasmid dna isolation - (reply: 1)
2184. Two stop codons - (reply: 1)
2185. About antibodies - How resistant are they (reply: 2)
2186. Vector needed - (reply: 1)
2187. Long PCR and genomic DNA isolation problems - (reply: 2)
2188. having the wrong vector in my clone - (reply: 3)
2189. Low Quality Seqeunces - (reply: 3)
2190. could FLAG-tagged protein be used in the Luc assay? - (reply: 1)