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$494.00
$3,000.00
$494.00
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usage
sufficient for 200 reactions
sufficient for 2000 reactions
Quality Level
feature
dNTPs included: no
hotstart
manufacturer/tradename
Roche
packaging
pkg of 200 x 50 μL reactions (04913850001)
pkg of 2000 x 50 μL reactions (04913914001)
technique(s)
RT-qPCR: suitable
qPCR: suitable
input
purified DNA
detection method
probe-based
1 of 4
This Item | L6544 | S9194 | S4438 |
|---|---|---|---|
| technique(s) RT-qPCR: suitable | technique(s) qPCR: suitable | technique(s) qPCR: suitable | technique(s) qPCR: suitable |
| usage sufficient for 200 reactions | usage sufficient for 100 reactions, sufficient for 2000 reactions, sufficient for 500 reactions | usage sufficient for 20 reactions, sufficient for 2000 reactions, sufficient for 400 reactions | usage sufficient for 100 reactions, sufficient for 20 reactions, sufficient for 500 reactions |
| feature dNTPs included: no | feature dNTPs included, hotstart | feature dNTPs included, hotstart | feature dNTPs included, hotstart |
| manufacturer/tradename Roche | manufacturer/tradename - | manufacturer/tradename - | manufacturer/tradename - |
| packaging pkg of 200 x 50 μL reactions (04913850001) | packaging - | packaging - | packaging - |
| input purified DNA | input purified DNA | input purified DNA | input purified DNA |
General description
SYBR® Green I is a DNA double-strand-specific dye. During each phase of DNA synthesis, the SYBR® Green I dye, which is included in the reaction mix, binds to the amplified PCR products. The amplicon can be detected by its fluorescence.
Hot start protocols have been shown to significantly improve the specificity, sensitivity, and yield of PCR. Heat-labile blocking groups on some of the amino acid residues of FastStart™ Taq DNA Polymerase make the modified enzyme inactive at room temperature (+15 to +25°C). Therefore, there is no elongation during the period when primers can non-specifically bind. FastStart™ Taq DNA Polymerase is activated by removing the blocking groups at a high temperature (i.e., a pre-incubation step at +95°C).
Application
Combine this master mix with Transcriptor First Strand cDNA Synthesis Kit (Roche) to achieve excellent results in two-step qRT-PCR.
FastStart™ Universal SYBR® Green Master (Rox) has been used in qRT-PCR[1][2][3][4][5] and qPCR[6][7][8][9]
Features and Benefits
- Improve PCR sensitivity and specificity.
- Avoid over-estimation of qPCR results.
- Amplify and detect a broad range of DNA or cDNA targets.
- Save time and effort in qPCR preparation.
- Prevent false positives resulting from carryover contamination.
Analysis Note
Other Notes
Legal Information
related product
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
does not flash
Flash Point(C)
does not flash
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Articles
Watch these videos to learn how real time or quantitative PCR (qPCR) works and the benefits of both the SYBR Green-based and probe-based methods of qPCR assay.
Related Content
RT-qPCR detects specific targets with applications in gene expression and pathogen detection.
Polymerase chain reaction (PCR) is a technique for amplifying nucleic acid molecules and is commonly used in many applications, including RT-PCR, hot start PCR, end point PCR and more.
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