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