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91. no bands after pcr!!!! - (reply: 4)
92. Help with definitons for qPCR - (reply: 1)
93. Calibrator in qPCR - (reply: 7)
94. Experimental design for RT-PCR - (reply: 8)
95. Primer dilution - (reply: 7)
96. Calculation help - (reply: 6)
97. standards for qPCR and some other doubts - (reply: 9)
98. Plasma cortisol/corticosterone level analysis using qPCR - (reply: 1)
99. Technical Replicates vs Biological Replicates - (reply: 1)
100. pcr - (reply: 1)
101. Difference in synthesis - (reply: 1)
102. Standardizing cDNA concentration before doing PCR - (reply: 4)
103. Agarose Gel Electrophoresis - (reply: 1)
104. Volume of Primers - (reply: 4)
105. qPCR with different genes - (reply: 5)
106. PCR conditions unknown? - (reply: 10)
107. PCR anomaly in a mid-range dilution of the template - (reply: 2)
108. Reducing contamination in 16s PCR for metagenomic library prer - (reply: 4)
109. 2 peaks for identical sequences in HRM - (reply: 2)
110. PCR using very long oligos !!! - (reply: 4)
111. Housekeeping gene for Real Time PCR when comparing expression of genes across di - (reply: 1)
112. How to optimize a master mix kit? - (reply: 7)
113. pcr primer design - (reply: 6)
114. Please help (primer/ probe final volume calculations) - (reply: 1)
115. Primer design with EcoRI ends - (reply: 2)
116. qPCR normalization - (reply: 4)
117. Reference Gene/HKG- every plate - (reply: 2)
118. qPCR standard for lipase genes - (reply: 2)
119. PCR with overlapping primers only (primer extention) - (reply: 3)
120. Random chuck of nonsense in middle of PCR - (reply: 6)
92. Help with definitons for qPCR - (reply: 1)
93. Calibrator in qPCR - (reply: 7)
94. Experimental design for RT-PCR - (reply: 8)
95. Primer dilution - (reply: 7)
96. Calculation help - (reply: 6)
97. standards for qPCR and some other doubts - (reply: 9)
98. Plasma cortisol/corticosterone level analysis using qPCR - (reply: 1)
99. Technical Replicates vs Biological Replicates - (reply: 1)
100. pcr - (reply: 1)
101. Difference in synthesis - (reply: 1)
102. Standardizing cDNA concentration before doing PCR - (reply: 4)
103. Agarose Gel Electrophoresis - (reply: 1)
104. Volume of Primers - (reply: 4)
105. qPCR with different genes - (reply: 5)
106. PCR conditions unknown? - (reply: 10)
107. PCR anomaly in a mid-range dilution of the template - (reply: 2)
108. Reducing contamination in 16s PCR for metagenomic library prer - (reply: 4)
109. 2 peaks for identical sequences in HRM - (reply: 2)
110. PCR using very long oligos !!! - (reply: 4)
111. Housekeeping gene for Real Time PCR when comparing expression of genes across di - (reply: 1)
112. How to optimize a master mix kit? - (reply: 7)
113. pcr primer design - (reply: 6)
114. Please help (primer/ probe final volume calculations) - (reply: 1)
115. Primer design with EcoRI ends - (reply: 2)
116. qPCR normalization - (reply: 4)
117. Reference Gene/HKG- every plate - (reply: 2)
118. qPCR standard for lipase genes - (reply: 2)
119. PCR with overlapping primers only (primer extention) - (reply: 3)
120. Random chuck of nonsense in middle of PCR - (reply: 6)