S1816
SYBR® Green JumpStart™ Taq ReadyMix™ for Quantitative PCR, Capillary Formulation
SYBR® Green qPCR reagent for Roche LightCycler® capillary systems
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About This Item
Código UNSPSC:
41106300
NACRES:
NA.55
Productos recomendados
formulario
liquid
uso
sufficient for 100 reactions
sufficient for 400 reactions
Características
dNTPs included
hotstart
concentración
1 units/reaction (20 μL reaction volume)
técnicas
qPCR: suitable
color
colorless
entrada
purified DNA
compatibilidad
for use with Roche LightCycler 480
método de detección
SYBR® Green
Condiciones de envío
wet ice
temp. de almacenamiento
−20°C
Descripción general
SYBR® Green JumpStart™ Taq ReadyMix™, Capillary formulation combines the advantages of a hot start enzyme, JumpStart Taq, in a 2× concentrate ReadyMix specifically designed for use with capillary instruments, such as the Roche LightCycler® real-time thermal cycler. SYBR Green JumpStart Taq ReadyMix is an optimized formulation containing SYBR Green I dye, JumpStart Taq DNA Polymerase, 99% pure deoxynucleotides, buffer and stabilizers.
SYBR Green Taq ReadyMix is recommended for single product real-time amplification experiments and may also be used for evaluation of primer sequences prior to manufacture of fluorescent-labeled probes. Fluorescent labeled probes are not recommended for use with SYBR Green I dye.
SYBR Green Taq ReadyMix is recommended for single product real-time amplification experiments and may also be used for evaluation of primer sequences prior to manufacture of fluorescent-labeled probes. Fluorescent labeled probes are not recommended for use with SYBR Green I dye.
Aplicación
SYBR® Green JumpStart™ Taq ReadyMix™ for Quantitative PCR, Capillary Formulation has been used in a real-time quantitative polymerase chain reaction (RT-qPCR) and reverse transcription PCR (RT-PCR).
Características y beneficios
- Convenient 2× concentrate ReadyMix specifically designed for use with capillary instruments such as the Roche LightCycler® and is ideal for high throughput applications
- Increased specificity & target yield - JumpStart™ Taq polymerase prevents non-specific product resulting in more accurate CT values and improved quantitation
- This master mix allows consistency from one reaction to the next
- Designed to reduce the preparation time and minimize contamination from multiple pipetting steps
- The double-strand DNA-specific SYBR® Green I fluorescent dye is inexpensive, easy to use, and sensitive and is ideal for quantifying any DNA sequence
Envase
A tube of 25 mM MgCl2 is provided for easy optimization of the QPCR reaction.
Default reaction volume is 20 μL
100RXN is packaged as 1 X 1 mL
400RXN is packaged as 1 X 4 mL
100RXN is packaged as 1 X 1 mL
400RXN is packaged as 1 X 4 mL
Principio
SYBR Green I, a commonly used fluorescent DNA binding dye, binds all double-stranded DNA and detection is monitored by measuring the increase in fluorescence throughout the cycle. SYBR Green I has an excitation and emission maxima of 494 nm and 521 nm, respectively. Specificity of Sigma′s SYBR based QPCR detection is greatly enhanced by the incorporation of a hot-start mediated taq polymerase, JumpStart Taq.
The JumpStart Taq antibody inactivates the DNA polymerase at room temperature. When the temperature is raised above 70 °C in the first denaturation step of the cycling process, the complex dissociates and the polymerase becomes fully active. JumpStart Taq DNA polymerase prevents non-specific amplification resulting in more accurate CT values.
To prepare a reaction, 10 μL of ReadyMix is added to primers, template and water for a final reaction volume of 20 μL.
The JumpStart Taq antibody inactivates the DNA polymerase at room temperature. When the temperature is raised above 70 °C in the first denaturation step of the cycling process, the complex dissociates and the polymerase becomes fully active. JumpStart Taq DNA polymerase prevents non-specific amplification resulting in more accurate CT values.
To prepare a reaction, 10 μL of ReadyMix is added to primers, template and water for a final reaction volume of 20 μL.
Definición de unidad
One unit incorporates 10 nmol of total dNTPs into acid-precipitable DNA in 30 min at 74 °C.
Información legal
Use of this product is covered by one or more of the following US patents and corresponding patent claims outside the US: 5,994,056 and 6,171,785.. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser′s own internal research. No right under any other patent claim (such as apparatus or system claims in US Patent No. 6,814,934) and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser′s activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patents require a separate license from Roche. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.
JumpStart is a trademark of Sigma-Aldrich Co. LLC
LightCycler is a registered trademark of Roche
ReadyMix is a trademark of Sigma-Aldrich Co. LLC
SYBR is a registered trademark of Life Technologies
Producto relacionado
Referencia del producto
Descripción
Precios
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 1
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Artículos
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Protocolos
A protocol that can be used as a basic template for qPCR incorporating SYBR Green I DNA binding dye that is amenable to modification and applicable for use as validation for a set of primers.
Our SYBR Green qPCR Protocol is a method designed to detect accurate quantification of gene expression and RT-PCR reactions
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