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Merck
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文件

R4526

Sigma-Aldrich

定量PCR参考染料

100 ×, solution

别名:

qPCR参考染料, ROX

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About This Item

分類程式碼代碼:
41106300
NACRES:
NA.55

形狀

solution

用途

sufficient for ≥600 reactions

濃度

100 ×

技術

PCR: suitable

顏色

red

溶解度

water: soluble

儲存溫度

2-8°C

相关类别

一般說明

Sigma′定量聚合酶链反应（qPCR）参考染料是一种专有染料，用于实时PCR。在使用SYBR绿、分子探针或双标记探针化学进行实时检测时，它可以用于反应数据的标准化。 我们提供100×参考染料，最大激发和放射峰分别出现在586nm和605nm。ROX参考染料仪器设定符合qPCR参考染料检测。

應用

定量 PCR 参考染料已被用于:
  • 制备用于实时定量聚合酶链反应 （RT-qPCR）的预混液
  • 作为反应混合物的成分，用于通过定量聚合酶链式反应（qPCR）检测艰难梭菌
  • 通过 qPCR 分析细胞 DNA 污染程度

其他說明

定量PCR参考染料仅用于研发目的。不可用于药物、家庭或其他用途。

象形圖

Exclamation markEnvironment
GHS07,GHS09

訊號詞

Warning

危險分類

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

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves

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Partial deletion of rng (RNase G)-enhanced homoethanol fermentation of xylose by the non-transgenic Escherichia coli RM10
Manow R, et al.
Journal of Industrial Microbiology & Biotechnology, 39(7), 977-985 (2012)
Ryan Manow et al.
World journal of microbiology & biotechnology, 36(4), 59-59 (2020-04-03)
An endogenous homoethanol pathway (glucose/1.2 xylose => 2 pyruvate => 2 ethanol) was previously engineered in Escherichia coli SZ410 via eliminating acid-producing pathways and anaerobic expression of the pyruvate dehydrogenase complex (aceEF-lpd operon). This ethanologenic derivative was subsequently engineered through adaptive evolution and partial
Kevin Antoine Brown et al.
Infection control and hospital epidemiology, 39(8), 917-923 (2018-08-10)
Clostridium difficile spores play an important role in transmission and can survive in the environment for several months. Optimal methods for measuring environmental C. difficile are unknown. We sought to determine whether increased sample surface area improved detection of C.
Gustav Johansson et al.
Molecular cancer therapeutics, 20(12), 2568-2576 (2021-09-24)
The majority of patients diagnosed with advanced gastrointestinal stromal tumors (GISTs) are successfully treated with a combination of surgery and tyrosine kinase inhibitors (TKIs). However, it remains challenging to monitor treatment efficacy and identify relapse early. Here, we utilized a
Sambrook, J. et al.
Molecular Cloning: A Laboratory Manual, 3rd (2000)
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