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New Forum Archives (2009-): :
211. RNA concentration is too low to detect gene of interest by qRT-PCR - (reply: 4)
213. Strange signals in the NTC - (reply: 1)
215. Autoclaving PCR waste in the room where PCRs are set up and run - Is it a proble - (reply: 2)
217. Assay question - (reply: 1)
219. HRM instrumentaion - (reply: 4)
221. Any online tool to check the propability of primer dimer formetion _ - (reply: 4)
223. PCR troubleshooting: wrong amplicon size when spiked into sample - (reply: 4)
225. Taqman probe in a LightCycler 480? - (reply: 1)
227. Ct value of housekeeping gene - (reply: 4)
229. Microfluidic PCR Issues, Master Mix and Consumable Variations? - (reply: 5)
231. If I am running Real-Time PCR with one gene of interest and one reference gene(G - (reply: 4)
233. Is this primer-dimer peak in my melting curve? - (reply: 6)
235. I'm working on an automated DD2CT value generator for Life tech qPCR machine - (reply: 2)
237. Reference gene(s) selection and validaton for qPCR - (reply: 5)
239. qPCR cannot detect reaction. - (reply: 1)
213. Strange signals in the NTC - (reply: 1)
215. Autoclaving PCR waste in the room where PCRs are set up and run - Is it a proble - (reply: 2)
217. Assay question - (reply: 1)
219. HRM instrumentaion - (reply: 4)
221. Any online tool to check the propability of primer dimer formetion _ - (reply: 4)
223. PCR troubleshooting: wrong amplicon size when spiked into sample - (reply: 4)
225. Taqman probe in a LightCycler 480? - (reply: 1)
227. Ct value of housekeeping gene - (reply: 4)
229. Microfluidic PCR Issues, Master Mix and Consumable Variations? - (reply: 5)
231. If I am running Real-Time PCR with one gene of interest and one reference gene(G - (reply: 4)
233. Is this primer-dimer peak in my melting curve? - (reply: 6)
235. I'm working on an automated DD2CT value generator for Life tech qPCR machine - (reply: 2)
237. Reference gene(s) selection and validaton for qPCR - (reply: 5)
239. qPCR cannot detect reaction. - (reply: 1)