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New Forum Archives (2009-): :
91. PCR Amplification Issues and Primer dimer - (reply: 4)
93. How to make PCR analysis using the 22DDCT Method - (reply: 1)
95. cDNA degradation within a week at -20? - (reply: 2)
97. Sec. structure in primers - (reply: 1)
99. Amount of RNA for cDNA - (reply: 4)
101. Changing PCR recipe halfway - (reply: 1)
103. Primer working with some cDNA samples and not other - (reply: 2)
105. Help with definitons for qPCR - (reply: 1)
107. Experimental design for RT-PCR - (reply: 8)
109. Calculation help - (reply: 6)
111. Plasma cortisol/corticosterone level analysis using qPCR - (reply: 1)
113. pcr - (reply: 1)
115. Standardizing cDNA concentration before doing PCR - (reply: 4)
117. Volume of Primers - (reply: 4)
119. PCR conditions unknown? - (reply: 10)
93. How to make PCR analysis using the 22DDCT Method - (reply: 1)
95. cDNA degradation within a week at -20? - (reply: 2)
97. Sec. structure in primers - (reply: 1)
99. Amount of RNA for cDNA - (reply: 4)
101. Changing PCR recipe halfway - (reply: 1)
103. Primer working with some cDNA samples and not other - (reply: 2)
105. Help with definitons for qPCR - (reply: 1)
107. Experimental design for RT-PCR - (reply: 8)
109. Calculation help - (reply: 6)
111. Plasma cortisol/corticosterone level analysis using qPCR - (reply: 1)
113. pcr - (reply: 1)
115. Standardizing cDNA concentration before doing PCR - (reply: 4)
117. Volume of Primers - (reply: 4)
119. PCR conditions unknown? - (reply: 10)