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91. PCR master mix containing primers and Taq - (reply: 4)
92. Primer working with some cDNA samples and not other - (reply: 2)
93. no bands after pcr!!!! - (reply: 4)
94. Help with definitons for qPCR - (reply: 1)
95. Calibrator in qPCR - (reply: 7)
96. Experimental design for RT-PCR - (reply: 8)
97. Primer dilution - (reply: 7)
98. Calculation help - (reply: 6)
99. standards for qPCR and some other doubts - (reply: 9)
100. Plasma cortisol/corticosterone level analysis using qPCR - (reply: 1)
101. Technical Replicates vs Biological Replicates - (reply: 1)
102. pcr - (reply: 1)
103. Difference in synthesis - (reply: 1)
104. Standardizing cDNA concentration before doing PCR - (reply: 4)
105. Agarose Gel Electrophoresis - (reply: 1)
106. Volume of Primers - (reply: 4)
107. qPCR with different genes - (reply: 5)
108. PCR conditions unknown? - (reply: 10)
109. PCR anomaly in a mid-range dilution of the template - (reply: 2)
110. Reducing contamination in 16s PCR for metagenomic library prer - (reply: 4)
111. 2 peaks for identical sequences in HRM - (reply: 2)
112. PCR using very long oligos !!! - (reply: 4)
113. Housekeeping gene for Real Time PCR when comparing expression of genes across di - (reply: 1)
114. How to optimize a master mix kit? - (reply: 7)
115. pcr primer design - (reply: 6)
116. Please help (primer/ probe final volume calculations) - (reply: 1)
117. Primer design with EcoRI ends - (reply: 2)
118. qPCR normalization - (reply: 4)
119. Reference Gene/HKG- every plate - (reply: 2)
120. qPCR standard for lipase genes - (reply: 2)
92. Primer working with some cDNA samples and not other - (reply: 2)
93. no bands after pcr!!!! - (reply: 4)
94. Help with definitons for qPCR - (reply: 1)
95. Calibrator in qPCR - (reply: 7)
96. Experimental design for RT-PCR - (reply: 8)
97. Primer dilution - (reply: 7)
98. Calculation help - (reply: 6)
99. standards for qPCR and some other doubts - (reply: 9)
100. Plasma cortisol/corticosterone level analysis using qPCR - (reply: 1)
101. Technical Replicates vs Biological Replicates - (reply: 1)
102. pcr - (reply: 1)
103. Difference in synthesis - (reply: 1)
104. Standardizing cDNA concentration before doing PCR - (reply: 4)
105. Agarose Gel Electrophoresis - (reply: 1)
106. Volume of Primers - (reply: 4)
107. qPCR with different genes - (reply: 5)
108. PCR conditions unknown? - (reply: 10)
109. PCR anomaly in a mid-range dilution of the template - (reply: 2)
110. Reducing contamination in 16s PCR for metagenomic library prer - (reply: 4)
111. 2 peaks for identical sequences in HRM - (reply: 2)
112. PCR using very long oligos !!! - (reply: 4)
113. Housekeeping gene for Real Time PCR when comparing expression of genes across di - (reply: 1)
114. How to optimize a master mix kit? - (reply: 7)
115. pcr primer design - (reply: 6)
116. Please help (primer/ probe final volume calculations) - (reply: 1)
117. Primer design with EcoRI ends - (reply: 2)
118. qPCR normalization - (reply: 4)
119. Reference Gene/HKG- every plate - (reply: 2)
120. qPCR standard for lipase genes - (reply: 2)