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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
121. Use of DMSO in General PCR - (reply: 1)
122. PCR product size confusion - (reply: 3)
123. Concentration specification in PCR - (reply: 3)
124. help us understand the run - (reply: 1)
125. Different MOI in comparison experiment - (reply: 3)
126. How to determine the size of gene to amplify? - (reply: 1)
127. Guanidine isothiocyanate in PCR - (reply: 1)
128. Untreated samples negative, how to analyze fold change? - (reply: 1)
129. Primers have worked well but now getting primer dimers? - (reply: 2)
130. I cannot design primers on exon-exon junction - (reply: 2)
131. DNA Quantification of PCR Products - (reply: 2)
132. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
133. Problem for PCR - (reply: 9)
134. Confused about my CT values - (reply: 1)
135. Designing primers in UTRs - (reply: 1)
136. Multiplex PCR - (reply: 1)
137. primer design@ buy? - (reply: 2)
138. High Ct/Cq values in my NO-RT and NTC samples - (reply: 3)
139. Dissolving DNA Oligos - (reply: 2)
140. Trouble with overlap extension pcr - (reply: 3)
141. copies per ul to copies per gram tissue - (reply: 2)
142. designing primers( selecting target sequence/amplicon design) - (reply: 3)
143. Question about the RT PCR - (reply: 3)
144. PCR ready mixes with long shelf lives - (reply: 4)
145. Problem with repeatability of the standard curve - (reply: 3)
146. Influenza virus - (reply: 3)
147. Defining standards in qPCR softwares - (reply: 3)
148. How to design primer to amplify genomic DNA? - (reply: 3)
149. Overlap PCR, need help - (reply: 11)
150. Internal control for miRNA RT-PCR - (reply: 1)