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Merck

S9194

Sigma-Aldrich

SYBR® Green JumpStart Taq ReadyMix for High Throughput qPCR

SYBR® Green qPCR reagent, passive reference dye included

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About This Item

UNSPSCコード:
41106300
NACRES:
NA.55

品質水準

形状

liquid

使用法

sufficient for 20 reactions
sufficient for 2000 reactions
sufficient for 400 reactions

特徴

dNTPs included
hotstart

濃度

1.25 units/reaction (50 μL reaction volume)

テクニック

qPCR: suitable

colorless

入力

purified DNA

適合性

for use with ABI 5700
for use with ABI 7000
for use with ABI 7300
for use with ABI 7700
for use with ABI 7900 Fast
for use with ABI 7900 HT
for use with ABI 7900
for use with ABI StepOne
for use with ABI StepOnePlus

検出方法

SYBR® Green

輸送温度

wet ice

保管温度

−20°C

関連するカテゴリー

詳細

SYBR® Green JumpStart Taq ReadyMix is a ready-to-use 2X master mix that contains SYBR® Green I, JumpStart Taq DNA polymerase, 99% pure deoxynucleotides (dNTPs), and reaction buffer making it the ideal solution for performing high-throughput quantitative PCR. SYBR® Green I dye binds to and detects any dsDNA generated during amplification. The JumpStart Taq DNA polymerase is an antibody-inactivated hot-start enzyme. Once the reaction temperature reaches 70°C, the DNA polymerase-antibody complex dissociates and Taq DNA polymerase activity is restored. This antibody-enzyme complex allows for easy and convenient set-up with less contamination risk than manual hot-start techniques.

アプリケーション

SYBR® Green JumpStart Taq ReadyMix for High Throughput qPCR has been used for the amplification and quantification of transcripts to analyze gene expression in 2-step quantitative reverse transcription PCR (RT-qPCR). It has also been used for quantitative polymerase chain reaction (qPCR) of reverse-transcribed cDNA.

特徴および利点

  • The master mix allows consistency and reproducibility from one reaction to the next
  • Reduced set-up time as compared to manual or wax Hot Start methods
  • Reduced primer dimers
  • Allows for room temperature set-up; Ideal for high throughput, quantitative PCR application
  • SYBR® Green I dye binds to double-stranded DNA and is ideal for quantifying any DNA sequence. Detection is monitored by measuring the increase in fluorescence throughout cycling.
  • JumpStart Taq DNA polymerase prevents amplification of non-specific products while increasing target yield.
  • Internal Reference Dye is provided for reaction normalization. Maximum excitation and emission is 586 nm and 605 nm, respectively.
  • SYBR Green JumpStart Taq ReadyMix reduces preparation time and the risk of contamination from multiple pipetting steps.

包装

Default reaction volume is 50 μL

20RXN is packaged as 1 X 500 μL
400RXN is packaged as 1 X 10 mL
2000RXN is packaged as 1 X 50 mL

その他情報

SYBR Green ReadyMix for High Throughput Quantitative PCR combines the performance enhancements of JumpStart Taq and SYBR Green I in an easy-to-use ReadyMix solution that incorporates ROX dye for ABI and other real time instrument applications. The ReadyMix includes a detection fluor, internal standard and reagents for PCR making it the ideal solution for performing high-throughput quantitative PCR.

法的情報

本製品を使用する場合、米国特許番号 5,994,056、6,171,785と、対応する米国外での特許請求のうち、1つ以上が適用されます。本製品の購入について、購入者自身の内部研究のために購入した量を使用する場合に限り、前述の特許請求に基づく訴訟から免責されますが、これは限定的なものであり、譲渡することはできません。他の特許請求(米国特許番号6,814,934に含まれる装置やシステムなど)によって保護されている権利や、あらゆる種類の商業サービス(購入者の研究結果を報酬やその他の商業的事由のために無制限に報告することを含む)を行う権利が、暗示や禁反言によって明示的に譲渡されるわけではありません。本製品は研究目的専用です。Rocheの特許に基づき診断に利用する場合は、別途Rocheからライセンスを受ける必要があります。ライセンス購入に関する詳細な情報については、ライセンス管理者(Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA)にお問い合わせ下さい。
JumpStart is a trademark of Sigma-Aldrich Co. LLC
ReadyMix is a trademark of Sigma-Aldrich Co. LLC
SYBR is a registered trademark of Life Technologies

ピクトグラム

Exclamation markEnvironment

シグナルワード

Warning

危険有害性情報

危険有害性の分類

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

保管分類コード

10 - Combustible liquids

WGK

WGK 3


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

S9194-VAR-PW:
S9194-400RXN:
S9194-BULK:
S9194-2000RXN:
S9194-20RXN:
S9194-2000RXN-PW:
S9194-PH:
S9194-400RXN-PW:
S9194-20RXN-KC:
S9194-20RXN-PW:
S9194-VAR:


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

Narcisa Muresu et al.
International journal of environmental research and public health, 17(12) (2020-06-27)
Objectives: Anal cancer is a rare disease. However, its incidence is increasing in some population groups. Infection caused by Human Papillomavirus (HPV) is strongly associated with the risk of anal cancer, whose variability depends on samples, histology, and HPV detection
Sambrook, J., and Russell, D.W.
Molecular Cloning: A Laboratory Manual null
Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin-repressive pathways
<BIG><BIG>Jullien J, et al.</BIG></BIG>
Molecular Cell, 873-884 (2017)
Gene resistance to transcriptional reprogramming following nuclear transfer is directly mediated by multiple chromatin-repressive pathways
Jullien J, et al.
Molecular Cell, 65(5), 873-884 (2017)
Shin-Heng Chiou et al.
Cancer discovery, 7(10), 1184-1199 (2017-08-10)
Pancreatic ductal adenocarcinoma (PDAC) is one of the most metastatic and deadly cancers. Despite the clinical significance of metastatic spread, our understanding of molecular mechanisms that drive PDAC metastatic ability remains limited. By generating a genetically engineered mouse model of

資料

Quantitative PCR (qPCR) provides information about gene expression, gene amplification or loss, and small alterations. qPCR is often used to investigate tumor biology and to discover the genetic and epigenetic causes of cancer

The polymerase chain reaction is one of the most widely used techniques in molecular biology. The PCR process consists of three main steps, Denaturation, Annealing & Extension

プロトコル

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

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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