Ugrás a tartalomra
Merck

FSUSGMMRO

Roche

FastStart Universal SYBR Green Master (Rox)

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
41106300
NACRES:
NA.55

használat

sufficient for 200 reactions
sufficient for 2000 reactions

Minőségi szint

Jellemzők

dNTPs included: no
hotstart

gyártó/kereskedő neve

Roche

kiszerelés

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

technika/technikák

RT-qPCR: suitable
qPCR: suitable

bemenet

purified DNA

észlelési módszer

probe-based

Általános leírás

FastStart Universal SYBR® Green Master (Rox) is a ready-to-use hot start reaction mix for qPCR and RT-qPCR on all real-time PCR systems requiring normalization with ROX.

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).

Alkalmazás

FastStart Universal SYBR® Green Master (Rox) can be used for the amplification and detection of any DNA or cDNA target, including those that are GC- or AT-rich.
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 and qPCR

Tulajdonságok és előnyök

  • Improve PCR sensitivity and specificity.
Minimize the formation of nonspecific amplification products.

  • Avoid over-estimation of qPCR results.
Eliminate nonspecific amplification products and primer-dimers that increase the amount of bound quantified SYBR Green I.
  • 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.

  • Save time and effort in qPCR preparation.
Eliminate the need to mix components, titrate MgCl2, or perform other time-consuming optimization steps.

  • 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.

Komponensek

FastStart Universal SYBR Green Master (Rox), 2x concentrated master mix that contains FastStart Taq DNA Polymerase, Reaction Buffer, Nucleotides (dATP, dCTP, dGTP, dUTP), SYBR Green I, and a reference dye.

Minőség

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).

Egyéb megjegyzések

For life science research only. Not for use in diagnostic procedures.

Jogi információk

FastStart is a trademark of Roche
SYBR is a registered trademark of Life Technologies

gyakran vásárolják ezzel a termékkel együtt

Product No.
Leírás
Árazás

Tárolási osztály kódja

12 - Non Combustible Liquids

WGK

WGK 1

Lobbanási pont (F)

does not flash

Lobbanási pont (C)

does not flash


Analitikai tanúsítványok (COA)

Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.

Már rendelkezik ezzel a termékkel?

Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Regulation of vascular endothelial growth factor (VEGF) splicing from pro-angiogenic to anti-angiogenic isoforms a novel therapeutic strategy for angiogenesis.
Nowak D G, et al.
The Journal of Biological Chemistry, 285(8), 5532-5540 (2010)
Lysine-specific demethylase 2B (KDM2B)-let-7-enhancer of zester homolog 2 (EZH2) pathway regulates cell cycle progression and senescence in primary cells.
Tzatsos A, et al.
The Journal of Biological Chemistry, 286(38), 33061-33069 (2011)
The Kruppel-like factor 15 as a molecular link between myogenic factors and a chromosome 4q transcriptional enhancer implicated in facioscapulohumeral dystrophy.
Dmitriev P, et al.
The Journal of Biological Chemistry, 286(52), 44620-44631 (2011)
USP18 establishes the transcriptional and anti-proliferative interferon α/β differential.
Veronique F N, et al.
The Biochemical Journal, 446(3), 509-516 (2012)
Assessment of mTOR-dependent translational regulation of interferon stimulated genes.
Livingstone M, et al.
PLoS ONE, 10(7), e0133482-e0133482 (2015)

Cikkek

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.

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

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.

A polimeráz láncreakció (PCR) a nukleinsavmolekulák felerősítésére szolgáló technika, amelyet számos alkalmazásban, többek között az RT-PCR, a hot start PCR, a végpont PCR és más alkalmazásokban használnak.

RT-qPCR detects specific targets with applications in gene expression and pathogen detection.

Az RT-qPCR specifikus célpontokat detektál, amelyek a génexpresszió és a kórokozók kimutatásában alkalmazhatók.

Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.

Lépjen kapcsolatba a szaktanácsadással