C60.amp: qPCR Experiment for the Amplification of MLC-2v and Vimentin...
In michbur/chipPCR: Toolkit of Helper Functions to Pre-Process Amplification Data

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Dilution experiment and metling curve (C60.melt) for the human genes MLC-2v and Vimentin (see Roediger et al. 2013) using the Roch Light Cycler 1.5.

1	data(C60.amp)

A data frame with 45 observations on the following 33 variables.

Index: Index of Cycles
Vim.0.1: Vimentin water control
Vim.0.2: Vimentin water control
Vim.1.1: Vimentin 10^-3 diluted
Vim.1.2: Vimentin 10^-3 diluted
Vim.2.1: Vimentin 10^-4 diluted
Vim.2.2: Vimentin 10^-4 diluted
Vim.3.1: Vimentin 10^-5 diluted
Vim.3.2: Vimentin 10^-5 diluted
Vim.4.1: Vimentin 10^-6 diluted
Vim.4.2: Vimentin 10^-6 diluted
Vim.5.1: Vimentin 10^-7 diluted
Vim.5.2: Vimentin 10^-7 diluted
Vim.6.1: Vimentin 10^-8 diluted
Vim.6.2: Vimentin 10^-8 diluted
Vim.7.1: Vimentin 10^-9 diluted
Vim.7.2: Vimentin 10^-9 diluted
MLC2v.1.1: MLC-2v 10^-3 diluted
MLC2v.1.2: MLC-2v 10^-3 diluted
MLC2v.2.1: MLC-2v 10^-4 diluted
MLC2v.2.2: MLC-2v 10^-4 diluted
MLC2v.3.1: MLC-2v 10^-5 diluted
MLC2v.3.2: MLC-2v 10^-5 diluted
MLC2v.4.1: MLC-2v 10^-6 diluted
MLC2v.4.2: MLC-2v 10^-6 diluted
MLC2v.5.1: MLC-2v 10^-7 diluted
MLC2v.5.2: MLC-2v 10^-7 diluted
MLC2v.6.1: MLC-2v 10^-8 diluted
MLC2v.6.2: MLC-2v 10^-8 diluted
MLC2v.7.1: MLC-2v 10^-9 diluted
MLC2v.7.2: MLC-2v 10^-9 diluted
MLC2v.0.1: MLC-2v water control
MLC2v.0.2: MLC-2v water control

MLC-2v and Vimentin were amplified in the Roche Light Cycler 1.5. Decadic dilutions of the input cDNA were prepared. The change of fluorescence was simultaneously monitored with EvaGreen. The primer sequences for MLC-2v were taken from Roediger et al. (2013). A 10 micro L qPCR reaction was composed of 250 nM primer (forward and reverse), Roche qPCR Master-Mix (according to the manufactures recommendations) and 1 micro L input DNA. EvaGreen was used at 1x final. During the amplification was monitored 58 degrees Celsius. Temperature profile:

95 deg C for 8 minutes 40 x 95 deg C for 10 sec 58 deg C for 15 sec 69 deg C for 25 sec

Stefan Roediger, Claudia Deutschmann (BTU Cottbus - Senftenberg)

A Highly Versatile Microscope Imaging Technology Platform for the Multiplex Real-Time Detection of Biomolecules and Autoimmune Antibodies. S. Roediger, P. Schierack, A. Boehm, J. Nitschke, I. Berger, U. Froemmel, C. Schmidt, M. Ruhland, I. Schimke, D. Roggenbuck, W. Lehmann and C. Schroeder. Advances in Biochemical Bioengineering/Biotechnology. 133:33–74, 2013.

Mao, F., Leung, W.-Y., Xin, X., 2007. Characterization of EvaGreen and the implication of its physicochemical properties for qPCR applications. BMC Biotechnol. 7, 76.