Competitive RNA templates for detection and quantitation of growth factors, cytokines, extracellular matrix components and matrix metalloproteinases by RT-PCR

Detection of low-abundance mRNAs by reverse transcription-polymerase chain reaction (RT-PCR) has become a standard technique to determine gene expression by tissues and cells in culture. The ability to determine relative or absolute copy number of specific mRNAs has been difficult due to inadequate...

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Veröffentlicht in:BioTechniques. - 1993. - 20(1996), 4 vom: 01. Apr., Seite 670-4
1. Verfasser: Tarnuzzer, R W (VerfasserIn)
Weitere Verfasser: Macauley, S P, Farmerie, W G, Caballero, S, Ghassemifar, M R, Anderson, J T, Robinson, C P, Grant, M B, Humphreys-Beher, M G, Franzen, L, Peck, A B, Schultz, G S
Format: Aufsatz
Sprache:English
Veröffentlicht: 1996
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Technical Report Journal Article Cytokines Extracellular Matrix Proteins Growth Substances RNA, Messenger Metalloendopeptidases EC 3.4.24.-
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245 1 0 |a Competitive RNA templates for detection and quantitation of growth factors, cytokines, extracellular matrix components and matrix metalloproteinases by RT-PCR 
264 1 |c 1996 
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500 |a Date Revised 21.03.2022 
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520 |a Detection of low-abundance mRNAs by reverse transcription-polymerase chain reaction (RT-PCR) has become a standard technique to determine gene expression by tissues and cells in culture. The ability to determine relative or absolute copy number of specific mRNAs has been difficult due to inadequate internal standards to control for sample-to-sample variation. The use of a synthetic RNA standard with identical sequences to the PCR primers allows reproducible quantitation between samples and assays. By designing multi-sequence templates, several specific mRNAs can be quantitated using a single template. Addition of multiple templates to a single RT reaction allows the quantitation of a large number of targets from as little as 4 micrograms of total RNA. In this report, we present a series of seven primer/template systems to detect and quantitate 52 specific messages, including 26 growth factors and receptors, 8 extracellular matrix components, 10 matrix-modifying enzymes and their inhibitors and 8 cytokines 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
650 4 |a Research Support, U.S. Gov't, P.H.S. 
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650 4 |a Journal Article 
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700 1 |a Macauley, S P  |e verfasserin  |4 aut 
700 1 |a Farmerie, W G  |e verfasserin  |4 aut 
700 1 |a Caballero, S  |e verfasserin  |4 aut 
700 1 |a Ghassemifar, M R  |e verfasserin  |4 aut 
700 1 |a Anderson, J T  |e verfasserin  |4 aut 
700 1 |a Robinson, C P  |e verfasserin  |4 aut 
700 1 |a Grant, M B  |e verfasserin  |4 aut 
700 1 |a Humphreys-Beher, M G  |e verfasserin  |4 aut 
700 1 |a Franzen, L  |e verfasserin  |4 aut 
700 1 |a Peck, A B  |e verfasserin  |4 aut 
700 1 |a Schultz, G S  |e verfasserin  |4 aut 
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