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S1816

Sigma-Aldrich

SYBR® Green JumpStart Taq ReadyMix for Quantitative PCR, Capillary Formulation

SYBR® Green qPCR reagent for Roche LightCycler® capillary systems

NACRES:
NA.55

form

liquid

usage

sufficient for 100 reactions
sufficient for 400 reactions

feature

dNTPs included
hotstart

concentration

1 units/reaction (20 μL reaction volume)

technique(s)

qPCR: suitable

color

colorless

input

purified DNA

compatibility

for use with Roche LightCycler 480

detection method

SYBR® Green

shipped in

wet ice

storage temp.

−20°C

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KCQS03KCQS02KCQS01
form

liquid

form

liquid

form

liquid

form

liquid

usage

sufficient for 100 reactions

usage

sufficient for 1250 reactions, sufficient for 250 reactions, sufficient for 5000 reactions

usage

sufficient for 1250 reactions, sufficient for 250 reactions, sufficient for 5000 reactions

usage

sufficient for 1250 reactions, sufficient for 250 reactions, sufficient for 5000 reactions

feature

dNTPs included

feature

dNTPs included, hotstart

feature

dNTPs included, hotstart

feature

dNTPs included, hotstart

concentration

1 units/reaction (20 μL reaction volume)

concentration

-

concentration

-

concentration

-

color

colorless

color

colorless

color

colorless

color

colorless

General description

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.

Application

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).

Features and Benefits

  • 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

Packaging

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

Principle

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.

Unit Definition

One unit incorporates 10 nmol of total dNTPs into acid-precipitable DNA in 30 min at 74 °C.

Legal Information

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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H Wouter Wisselink et al.
Applied and environmental microbiology, 73(15), 4881-4891 (2007-06-05)
For cost-effective and efficient ethanol production from lignocellulosic fractions of plant biomass, the conversion of not only major constituents, such as glucose and xylose, but also less predominant sugars, such as l-arabinose, is required. Wild-type strains of Saccharomyces cerevisiae, the
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The Journal of international medical research, 49(6), 3000605211013548-3000605211013548 (2021-07-01)
Long non-coding RNA (lncRNA) expression is closely related to the pathogenesis and progression of various tumors. In this study, we investigated the mechanisms of lncRNA HOXB cluster antisense RNA 3 (HOXB-AS3), miRNA(miR)-498-5p, and disintegrin and metalloproteinase domain-containing protein 9 (ADAM9)
Sambrook, J., et al.
Molecular Cloning: A Laboratory Manual, Third Edition (2000)
Aifeng Liu et al.
Journal of nanoscience and nanotechnology, 19(1), 91-97 (2018-10-18)
Osteoarthritis (OA) is an unavoidable degenerative disease of the human body. A relatively efficient and desirable treatment exists that leads to the ecological restoration of cartilage through the adjustments of the micro-environment of the human body and relies on its
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Journal of molecular endocrinology, 29(1), 23-39 (2002-08-30)
The fluorescence-based real-time reverse transcription PCR (RT-PCR) is widely used for the quantification of steady-state mRNA levels and is a critical tool for basic research, molecular medicine and biotechnology. Assays are easy to perform, capable of high throughput, and can

Articles

Using Probe-Based Quantitative PCR (Qpcr) to Measure Gene-Level Expression

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