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1801. Sequencing of scarce real-time amplicons - (reply: 1)
1802. PCR efficiency important in real time absolute quantification? - (reply: 4)
1803. PCR contamination with human DNA first and now no bands!!! - (reply: 4)
1804. Genotyping PCR - (reply: 3)
1805. Is this standard valid? - pcr product as standards (reply: 5)
1806. geNorm NF calculation - normalization in geNorm (reply: 5)
1807. primer binding - (reply: 1)
1808. Real time 70% efficiency and DDCt - (reply: 1)
1809. RNA visualization - (reply: 1)
1810. PCR primers - (reply: 1)
1811. amplification in negative control in RT PCR - (reply: 2)
1812. 18S changes with cDNA dilution - (reply: 2)
1813. Deletion PCR - (reply: 9)
1814. crossing point - crossing point (reply: 2)
1815. Smear problem with my new primer set - (reply: 2)
1816. PCR ghost bands - (reply: 1)
1817. wash buffer for columns - how to make it? (reply: 3)
1818. amplicon storage - amplicon storage (reply: 3)
1819. CP of real time PCR by LC480 - (reply: 1)
1820. transient expression - best time to detect the mRNA? (reply: 1)
1821. Chosing the best housekeeping gene! - (reply: 5)
1822. real-time PCR and HIV - what is the most commonly used assay to measure viral load in plasma (reply: 2)
1823. Unspecific PCR - (reply: 7)
1824. Real-Time PCR as a Microplate Reader - (reply: 1)
1825. RT-PCR Internal Standard - (reply: 2)
1826. Differences in Thermal Cyclers? - (reply: 1)
1827. ssDNA Quantification - (reply: 4)
1828. Standards for The Relative Standard Curve Method - (reply: 3)
1829. RNA contamination in PCR - (reply: 1)
1830. DNase I pre-treatment - how can i be sure that it was efficient??? (reply: 2)
1802. PCR efficiency important in real time absolute quantification? - (reply: 4)
1803. PCR contamination with human DNA first and now no bands!!! - (reply: 4)
1804. Genotyping PCR - (reply: 3)
1805. Is this standard valid? - pcr product as standards (reply: 5)
1806. geNorm NF calculation - normalization in geNorm (reply: 5)
1807. primer binding - (reply: 1)
1808. Real time 70% efficiency and DDCt - (reply: 1)
1809. RNA visualization - (reply: 1)
1810. PCR primers - (reply: 1)
1811. amplification in negative control in RT PCR - (reply: 2)
1812. 18S changes with cDNA dilution - (reply: 2)
1813. Deletion PCR - (reply: 9)
1814. crossing point - crossing point (reply: 2)
1815. Smear problem with my new primer set - (reply: 2)
1816. PCR ghost bands - (reply: 1)
1817. wash buffer for columns - how to make it? (reply: 3)
1818. amplicon storage - amplicon storage (reply: 3)
1819. CP of real time PCR by LC480 - (reply: 1)
1820. transient expression - best time to detect the mRNA? (reply: 1)
1821. Chosing the best housekeeping gene! - (reply: 5)
1822. real-time PCR and HIV - what is the most commonly used assay to measure viral load in plasma (reply: 2)
1823. Unspecific PCR - (reply: 7)
1824. Real-Time PCR as a Microplate Reader - (reply: 1)
1825. RT-PCR Internal Standard - (reply: 2)
1826. Differences in Thermal Cyclers? - (reply: 1)
1827. ssDNA Quantification - (reply: 4)
1828. Standards for The Relative Standard Curve Method - (reply: 3)
1829. RNA contamination in PCR - (reply: 1)
1830. DNase I pre-treatment - how can i be sure that it was efficient??? (reply: 2)