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Roche

FastStart Universal Probe Master (Rox)

sufficient for 250 reactions, sufficient for 1250 reactions, sufficient for 5000 reactions, suitable for qPCR, suitable for RT-qPCR

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250 x 20 reactions

Available to ship TODAYfromMILWAUKEE

$216.00
1250 x 20 reactions

Available to ship TODAYfromMILWAUKEE

$1,010.00
5000 x 20 reactions

Available to ship TODAYfromMILWAUKEE

$3,640.00

About This Item

NACRES:
NA.55
UNSPSC Code:
41106300

$216.00


Available to ship TODAYDetails


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usage

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

feature

dNTPs included: no, hotstart

manufacturer/tradename

Roche

packaging

pkg of 1250 x 20 μL reactions (04913957001), pkg of 250 x 20 μL reactions (04913949001), pkg of 5000 x 20 μL reactions (04914058001)

technique(s)

RT-qPCR: suitable, qPCR: suitable

input

purified DNA

detection method

probe-based

General description

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. Therefore, there is no elongation during the period when primers can nonspecifically bind. FastStart Taq DNA Polymerase is activated by removing the blocking groups at a high temperature (i.e., a preincubation step at +95°C).
Universal ready-to-use hot start reaction mix for qPCR and RT-qPCR on all real-time PCR systems requiring normalization with ROX.

FastStart Universal Probe Master (Rox) includes a novel reference dye that enables its use on all real-time PCR instruments requiring normalization with ROX, without modification or adjustments to the specific instrument or protocol. This ready-to-use, 2x concentrated master mix contains all reagents (except primers, probe, and template) needed for running quantitative, real-time DNA-detection assays, including qPCR and two-step qRT-PCR, in the hydrolysis probe detection format. FastStart Universal Probe Master (Rox) generates excellent results on instruments such as the Applied Biosystems 7900 HT Fast Real-Time PCR System or the Applied Biosystems 7500 Real-Time PCR System. This product is not intended for use with the LightCycler® Instruments.

Application

FastStart Universal Probe Master (Rox) has been used:
  • in TaqMan® quantitative real-time polymerase chain reaction (qRT-PCR) reactions for the quantification of endogenous miRNAs, such as MIR376B, MIR376A and MIR181A[1][2][3]
  • in reverse transcriptase (RT-PCR) to study tumor necrosis factor (TNF) expression in whole synovial tissue of undifferentiated peripheral inflammatory arthritis (UPIA) patients[4]
  • for the amplification and detection of any DNA or cDNA target, including those that are GC- or AT-rich by quantitativePCR[5][6]
Combine this master mix with Transcriptor First Strand cDNA Synthesis Kit (Roche) to achieve excellent results in two-step qRT-PCR.

Features and Benefits

  • Increase qPCR sensitivity and specificity.
Produce lower cycle threshold (Ct) values.

  • Use the master mix with any probe-based assay.
Achieve sensitive, specific results in assays with the Universal ProbeLibrary Probes or any other hydrolysis probe.

  • Amplify and detect a broad range of DNA or cDNA targets.
Amplify fragments up to 500 bp long, including those that are GC- or AT-rich.

  • Visualize amplification products on agarose gels.

  • Use robotic pipetting stations to set up qPCR reactions.
Use a master mix that is stable at room temperature during extended reaction setup times.

  • Prevent false positives resulting from carryover contamination.
Use this dUTP-containing mix with Uracil-DNA Glycosylase to eliminate contaminating DNA carried over from previous PCR reactions.

Analysis Note

Function test: Each lot is tested for performance in qPCR using three templates: a GC–rich template, an AT-rich template, and a long template (approximately 440 bp).

Other Notes

FastStart Universal Probe Master (Rox), 2x concentrated master mix that contains FastStart Taq DNA Polymerase, Reaction Buffer, Nucleotides (dATP, dCTP, dGTP, dUTP), and a reference dye.
For life science research only. Not for use in diagnostic procedures

Legal Information

FastStart is a trademark of Roche
LightCycler is a registered trademark of Roche
TaqMan is a registered trademark of Roche Molecular Systems, Inc.

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This Item
FSUSGMMROFSSGMMROFSTMPMMRO
technique(s)

RT-qPCR: suitable

technique(s)

RT-qPCR: suitable

technique(s)

RT-qPCR: suitable

technique(s)

RT-qPCR: suitable

detection method

probe-based

detection method

probe-based

detection method

probe-based

detection method

probe-based

usage

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

usage

sufficient for 200 reactions, sufficient for 2000 reactions

usage

sufficient for 500 reactions, sufficient for 5000 reactions

usage

sufficient for 100 reactions, sufficient for 2000 reactions, sufficient for 500 reactions

feature

hotstart, dNTPs included: no

feature

dNTPs included: no, hotstart

feature

dNTPs included, hotstart

feature

dNTPs included: no, hotstart

packaging

pkg of 1250 x 20 μL reactions (04913957001), pkg of 5000 x 20 μL reactions (04914058001), pkg of 250 x 20 μL reactions (04913949001)

packaging

pkg of 200 x 50 μL reactions (04913850001), pkg of 2000 x 50 μL reactions (04913914001)

packaging

pkg of 500 x 20 μL reactions (04673484001), pkg of 5000 x 20 μL reactions (04673492001)

packaging

pkg of 100 x 50 μL reactions (04673409001), pkg of 2000 x 50 μL reactions (04673433001), pkg of 500 x 50 μL reactions (04673417001)

input

purified DNA

input

purified DNA

input

purified DNA

input

purified DNA


Storage Class

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

does not flash

flash_point_c

does not flash



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Articles

The purpose of Hot Start PCR is to inhibit the PCR reaction in order to reduce nonspecific amplification, prevent the formation of primer dimers, and increase product yields.

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.

La reacción en cadena de la polimerasa (PCR) es una técnica de amplificación de moléculas de ácidos nucleicos y se utiliza habitualmente en muchas aplicaciones, entre ellas la RT-PCR (retroPCR), la PCR de inicio en caliente, la PCR de punto final.

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Kumsal Ayse Tekirdag et al.
Autophagy, 9(3), 374-385 (2013-01-17)
Macroautophagy (autophagy herein) is a cellular catabolic mechanism activated in response to stress conditions including starvation, hypoxia and misfolded protein accumulation. Abnormalities in autophagy were associated with pathologies including cancer and neurodegenerative diseases. Hence, elucidation of the signaling pathways controlling
Stefano Alivernini et al.
Frontiers in medicine, 5, 186-186 (2018-07-19)
Objectives: To examine synovial tissue (ST) predictors of clinical differentiation in patients with seronegative undifferentiated peripheral inflammatory arthritis (UPIA). Methods: Fourty-two patients with IgA/IgM-Rheumatoid Factor and anti-citrullinated peptide antibodies negative UPIA, naive to Disease-Modifying Anti-Rheumatic Drugs, underwent Gray Scale (GSUS)
Matthew L Hillestad et al.
Human gene therapy, 23(10), 1116-1126 (2012-07-28)
Reporter genes are important tools for assessing vector pharmacology in vivo. Although useful, current systems are limited by (1) the need to generate a new vector for each different reporter, (2) the inability to package reporter genes in small vectors



Global Trade Item Number

SKUGTIN
491395700104061838338082
491394900104061838338075
491405800104061838338105