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1111. PI needs something ASAP! - densitometry on westerns (reply: 1)
1112. DBA2J genome sequence - (reply: 1)
1113. how can I identify hemi- and homozygous individuals? - (reply: 1)
1114. Question about Primers - (reply: 3)
1115. Odd question. Can I use DNase to decontaminate Primers? - Primer decontamination (reply: 2)
1116. Possible solvents for RNA - (reply: 2)
1117. weird bands after minipreps - molecular cloning (reply: 2)
1118. Large fragment amplification failed - (reply: 3)
1119. purification of PCR product for cloning in a vector - (reply: 3)
1120. elimination of Protein interference from DNA - for RT-PCR (reply: 2)
1121. Transient transfection with viral vectors - Is it acceptable to do direct transfection with viral vectors? (reply: 1)
1122. Adapter ligation problem - (reply: 5)
1123. Primer design with a tag - (reply: 4)
1124. Lithium electrophoresis buffer - Why does it not work? (reply: 2)
1125. Weird migration of double digested plasmid - (reply: 4)
1126. Run agarose/formaldehyde gel for 5 mins before loading samples? Why? - (reply: 1)
1127. Myc tags - (reply: 1)
1128. MOPS: How do you sterlise yours? - (reply: 2)
1129. Which gel concentration - (reply: 4)
1130. Glyoxylated RNA and SYBR Safe - Running glyoxylated RNA on a SYBR safe agarose gel - NO BANDS (reply: 1)
1131. PCR Amplification: Tips on simple things to keep an eye out for - (reply: 1)
1132. MINI Dialysis Units - below 2K MWCO? (reply: 1)
1133. PCR for sequencing genomic DNA (multiple alleles) - Are there preferences for amplification of certain sequences? (reply: 1)
1134. Rotten Fish Smell in TAE Buffer - Stinky TAE (reply: 3)
1135. plasmid extraction and purification - methods to extract and purify plasmid to get high purity super coil (reply: 4)
1136. Combining forward and reverse primer gives different size on gel - (reply: 2)
1137. Help for co-transfection of proteins and plasmid - (reply: 1)
1138. PCR of complement genomic DNA - (reply: 3)
1139. RNAi is somatic and germline cells - (reply: 3)
1140. subcloning into bacterial expression vector - (reply: 1)
1112. DBA2J genome sequence - (reply: 1)
1113. how can I identify hemi- and homozygous individuals? - (reply: 1)
1114. Question about Primers - (reply: 3)
1115. Odd question. Can I use DNase to decontaminate Primers? - Primer decontamination (reply: 2)
1116. Possible solvents for RNA - (reply: 2)
1117. weird bands after minipreps - molecular cloning (reply: 2)
1118. Large fragment amplification failed - (reply: 3)
1119. purification of PCR product for cloning in a vector - (reply: 3)
1120. elimination of Protein interference from DNA - for RT-PCR (reply: 2)
1121. Transient transfection with viral vectors - Is it acceptable to do direct transfection with viral vectors? (reply: 1)
1122. Adapter ligation problem - (reply: 5)
1123. Primer design with a tag - (reply: 4)
1124. Lithium electrophoresis buffer - Why does it not work? (reply: 2)
1125. Weird migration of double digested plasmid - (reply: 4)
1126. Run agarose/formaldehyde gel for 5 mins before loading samples? Why? - (reply: 1)
1127. Myc tags - (reply: 1)
1128. MOPS: How do you sterlise yours? - (reply: 2)
1129. Which gel concentration - (reply: 4)
1130. Glyoxylated RNA and SYBR Safe - Running glyoxylated RNA on a SYBR safe agarose gel - NO BANDS (reply: 1)
1131. PCR Amplification: Tips on simple things to keep an eye out for - (reply: 1)
1132. MINI Dialysis Units - below 2K MWCO? (reply: 1)
1133. PCR for sequencing genomic DNA (multiple alleles) - Are there preferences for amplification of certain sequences? (reply: 1)
1134. Rotten Fish Smell in TAE Buffer - Stinky TAE (reply: 3)
1135. plasmid extraction and purification - methods to extract and purify plasmid to get high purity super coil (reply: 4)
1136. Combining forward and reverse primer gives different size on gel - (reply: 2)
1137. Help for co-transfection of proteins and plasmid - (reply: 1)
1138. PCR of complement genomic DNA - (reply: 3)
1139. RNAi is somatic and germline cells - (reply: 3)
1140. subcloning into bacterial expression vector - (reply: 1)