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1111. no bacterial growth after inoculation - (reply: 4)
1112. Low A260/A280 ratio after gel purification using Promega PCR Clean-up System - (reply: 2)
1113. Anoyone knows a good reliable gel documentation system? - (reply: 4)
1114. Isolating Genomic DNA from a small colony of cultured human cells - (reply: 1)
1115. how to seperate double-digestion products on agarose gel - (reply: 14)
1116. Insert lose in Phage display library - (reply: 6)
1117. Help: I am loosing the DNA during PCR purification - (reply: 7)
1118. PCR primer with no extra DNA end - (reply: 5)
1119. Relative promoter strength - (reply: 2)
1120. Dot Blot - Protein not adhering to membrane - (reply: 1)
1121. Protein contamination - How to remove all protein from my DNA? - (reply: 3)
1122. fluorescent -transfection problem - (reply: 1)
1123. extract plasmids from transfected eukaryotic cells - (reply: 6)
1124. I can't see anything in my gel. I need help - (reply: 1)
1125. Restriction digestion of clones give undesired product - (reply: 3)
1126. cDNA shelf-life - (reply: 1)
1127. Phenol peak at RNA isolation with Trizol method - (reply: 1)
1128. HELP!!!!absorbance peak and radioactivity do not match??? - (reply: 4)
1129. cell culture confusion - (reply: 1)
1130. COL E1 mutations in vector after sequencing - (reply: 1)
1131. Strange band in colony PCR - (reply: 2)
1132. stability of Phusion and Pfu at room temperature - (reply: 2)
1133. what does HLA-G stand for? - (reply: 4)
1134. saturation mutagenesis library problem again - (reply: 2)
1135. Multiplex PCR - (reply: 12)
1136. ISH probe choose - (reply: 1)
1137. Forcing overexpression of a GOI - (reply: 7)
1138. questions on cycloheximide pulse chase assay - (reply: 6)
1139. Ligation problem - (reply: 7)
1140. Strange question on TRIzol and RNAlater - (reply: 3)
1112. Low A260/A280 ratio after gel purification using Promega PCR Clean-up System - (reply: 2)
1113. Anoyone knows a good reliable gel documentation system? - (reply: 4)
1114. Isolating Genomic DNA from a small colony of cultured human cells - (reply: 1)
1115. how to seperate double-digestion products on agarose gel - (reply: 14)
1116. Insert lose in Phage display library - (reply: 6)
1117. Help: I am loosing the DNA during PCR purification - (reply: 7)
1118. PCR primer with no extra DNA end - (reply: 5)
1119. Relative promoter strength - (reply: 2)
1120. Dot Blot - Protein not adhering to membrane - (reply: 1)
1121. Protein contamination - How to remove all protein from my DNA? - (reply: 3)
1122. fluorescent -transfection problem - (reply: 1)
1123. extract plasmids from transfected eukaryotic cells - (reply: 6)
1124. I can't see anything in my gel. I need help - (reply: 1)
1125. Restriction digestion of clones give undesired product - (reply: 3)
1126. cDNA shelf-life - (reply: 1)
1127. Phenol peak at RNA isolation with Trizol method - (reply: 1)
1128. HELP!!!!absorbance peak and radioactivity do not match??? - (reply: 4)
1129. cell culture confusion - (reply: 1)
1130. COL E1 mutations in vector after sequencing - (reply: 1)
1131. Strange band in colony PCR - (reply: 2)
1132. stability of Phusion and Pfu at room temperature - (reply: 2)
1133. what does HLA-G stand for? - (reply: 4)
1134. saturation mutagenesis library problem again - (reply: 2)
1135. Multiplex PCR - (reply: 12)
1136. ISH probe choose - (reply: 1)
1137. Forcing overexpression of a GOI - (reply: 7)
1138. questions on cycloheximide pulse chase assay - (reply: 6)
1139. Ligation problem - (reply: 7)
1140. Strange question on TRIzol and RNAlater - (reply: 3)