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Top : New Forum Archives (2009-): : Molecular-Biology
121. qPCR acceptable standard deviation - (reply: 1)
122. Gel doubling banding and resolution problem - (reply: 6)
123. Canīt get rid of DNA contamination in RNA - (reply: 2)
124. PCR DNA bands too large on agarose gel - (reply: 1)
125. Easy to transfect primary cell line? - (reply: 1)
126. Sequence specific pulldown of dsDNA - (reply: 8)
127. Gene expression and transcription factors - (reply: 1)
128. RNA gel problem (melted bands) - (reply: 2)
129. RNA extraction and DNase treatment - (reply: 1)
130. Cloning purified PCR product into cells - (reply: 5)
131. Mention of Transgene Insertion into Cell Lines By Transfecting with cDNA - (reply: 2)
132. when to add polybrene for lentivirus transduction? - (reply: 1)
133. How to know the plasmid extracted are indeed the plasmid of interest? - (reply: 4)
134. In situ hybridization - (reply: 5)
135. Sypro Ruby Dye Front - (reply: 9)
136. Forced Expression vs. Enforced Expression - (reply: 1)
137. Co-immunoprecipitation non-specific binding - (reply: 2)
138. New webpage and software tools - (reply: 1)
139. What DCH5a cells are? / pCAMBIA1301 isolation from DHC5a cells - (reply: 3)
140. Can I snap freeze my tissue (liquid nitrogen) in Lysis buffer for later RNA extr - (reply: 6)
141. Gateway cloning not working. - (reply: 7)
142. Assays from very few number of cells - (reply: 1)
143. EM7 promoter - what is it? - (reply: 1)
144. Virus processing (filtration) of blood - How to? - (reply: 5)
145. ABC(D) Model of Plant Flowers - (reply: 1)
146. TE buffer pH adjustment - (reply: 1)
147. Estimate cost for Molecular Docking software/devices - (reply: 1)
148. Polymorphism - (reply: 2)
149. PCR_QUALITY CONTROL - (reply: 2)
150. Difficult cloning/ligation/transformation blunt and sticky - (reply: 1)