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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1111. Question of q-pcr primer design - Tm difference from IDTDNA (reply: 2)
1112. TELO2 & GAPDH - (reply: 2)
1113. PCR -No band formation - (reply: 1)
1114. 3' race - (reply: 1)
1115. PCR AMPLIFICATION - (reply: 1)
1116. internal control for genomic DNA - (reply: 1)
1117. qPCR Data Analysis - Software (reply: 3)
1118. Gene expression confusion - (reply: 5)
1119. real time pcr need advise - (reply: 2)
1120. Opinion about LUX primers /D-LUX assay - What say you? (reply: 5)
1121. ChIP-qPCR shift in melt curve - (reply: 4)
1122. Long PCR Primers? Advice for generating multiple adjacent mutations - Designing long degenerate primers for shotgun alanine scanning (reply: 3)
1123. use of housekeeping gene in RT PCR chIP - (reply: 3)
1124. what is the order you follow in the run ??? - in order to make the contamination risk the least (reply: 3)
1125. DNA pooling for PCR - Saving money PCR (reply: 7)
1126. Real Time PCR Standard curves - How many are required??? (reply: 1)
1127. pcr-rflp - (reply: 2)
1128. PCR need some help - (reply: 4)
1129. problems when use qPCR to quantify bisulfite modified DNA - (reply: 4)
1130. Left polymerase out overnight - Will it still work? (reply: 1)
1131. very low expression of a sample vs standard curve efficiency - (reply: 1)
1132. Primer Reconstitution--does temperature matter? - (reply: 5)
1133. TaqMan Gene Expression Assays - Low expression/ Ct values (reply: 2)
1134. Gradient PCR works, but single temperature does not! HELP!! - (reply: 5)
1135. Oligonucleotide degradation - (reply: 1)
1136. Primer efficiency - How to determine primer efficiency correctly? (reply: 4)
1137. never get bands by pfu related enzymes - (reply: 2)
1138. Primer design for qPCR - (reply: 1)
1139. Primer-BLAST... - (reply: 4)
1140. reporting results of qPCR - (reply: 1)