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New Forum Archives (2009-): :
1801. PCR efficiency important in real time absolute quantification? - (reply: 4)
1803. Genotyping PCR - (reply: 3)
1805. geNorm NF calculation - normalization in geNorm (reply: 5)
1807. Real time 70% efficiency and DDCt - (reply: 1)
1809. PCR primers - (reply: 1)
1811. 18S changes with cDNA dilution - (reply: 2)
1813. crossing point - crossing point (reply: 2)
1815. PCR ghost bands - (reply: 1)
1817. amplicon storage - amplicon storage (reply: 3)
1819. transient expression - best time to detect the mRNA? (reply: 1)
1821. real-time PCR and HIV - what is the most commonly used assay to measure viral load in plasma (reply: 2)
1823. Real-Time PCR as a Microplate Reader - (reply: 1)
1825. Differences in Thermal Cyclers? - (reply: 1)
1827. Standards for The Relative Standard Curve Method - (reply: 3)
1829. DNase I pre-treatment - how can i be sure that it was efficient??? (reply: 2)
1803. Genotyping PCR - (reply: 3)
1805. geNorm NF calculation - normalization in geNorm (reply: 5)
1807. Real time 70% efficiency and DDCt - (reply: 1)
1809. PCR primers - (reply: 1)
1811. 18S changes with cDNA dilution - (reply: 2)
1813. crossing point - crossing point (reply: 2)
1815. PCR ghost bands - (reply: 1)
1817. amplicon storage - amplicon storage (reply: 3)
1819. transient expression - best time to detect the mRNA? (reply: 1)
1821. real-time PCR and HIV - what is the most commonly used assay to measure viral load in plasma (reply: 2)
1823. Real-Time PCR as a Microplate Reader - (reply: 1)
1825. Differences in Thermal Cyclers? - (reply: 1)
1827. Standards for The Relative Standard Curve Method - (reply: 3)
1829. DNase I pre-treatment - how can i be sure that it was efficient??? (reply: 2)