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Merck
CN

A4464

Sigma-Aldrich

增强型禽逆转录酶 [eAMV RT]

For reverse transcription at higher temperatures & rare mRNAs

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About This Item

MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.55

质量水平

表单

crystalline powder

用途

sufficient for 50 reactions

特点

dNTPs included: no
hotstart: no

浓度

20 units/μL

技术

RT-PCR: suitable

颜色

colorless

输入

purified RNA

运输

wet ice

储存温度

−20°C

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一般描述

eAMV 逆转录酶是一种增强型禽成髓细胞病病毒(AMV)逆转录酶,负责合成与 RNA、DNA 或 RNA:DNA 杂交体互补的 DNA 链。这种异常强大的 AMV逆转录酶比标准 AMV 或 Moloney 鼠白血病病毒(M-MLV)逆转录酶具有更优的热稳定性。eAMV RT 是从总 RNA 或 poly(A)+RNA获得高质量全长 cDNA 的理想酶,并且在转录长靶标方面也是有效的。

应用

Enhanced Avian Reverse Transcriptase可将RNA转录为DNA,同时显著提升mRNA模板合成cDNA的效率。这是由于本款增强型AMV-RT能够逆转录长链mRNA模板,能够有效穿越复杂的二级结构,可以通过RT-PCR反应检测低丰度mRNA。
增强型禽逆转录酶[eAMV逆转录酶]已用于总 RNA 的逆转录,以在定量逆转录 PCR(RT-qPCR)分析中合成 cDNA。
增强型禽(eAMV)逆转录酶是一种高度纯化的禽成髓细胞瘤病毒逆转录酶(AMV-RT),与标准AMV-RT或标准莫洛尼鼠白血病病毒逆转录酶(MMLV-RT)相比,具有更高的性能。

这种异常的稳健AMV-RT具有增强的检测低丰度信息,在高温(高达65℃)下通过困难的二级结构转录以及转录高达14.1 kb的mRNA模板的能力。

生化/生理作用

逆转录酶能够加速dNTP形成磷酸二酯键,从而催化RNA模板整合到互补DNA中。

特点和优势

  • 对低丰度信使核糖核酸的敏感性更高
  • 在高温(高达 65°C)下通过复杂二级结构进行的无核转录
  • 高效生成高达 14.1kb的全长 cDNA
  • 产生可用于 PCR 扩增的第一链 cDNA

包装

提供1管10x反应缓冲液。

单位定义

一单位酶能够以多聚腺苷酸为模板,以12-18的oligo(dT)为引物,在10分钟内将1纳摩TMP整合进TCA沉淀材料中。

法律信息

Purchase of this product is accompanied by a limited license for use in the Polymerase Chain Reaction (PCR) process for research purposes only and in conjunction with a thermal cycler whose use in the automated performance of the PCR process is covered by an up-front license fee, either by payment to Applied Biosystems or as purchased, i.e., and authorized thermal cycler.
eAMV is a trademark of Sigma-Aldrich Co. LLC

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

常规特殊物品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Emily Schifano et al.
Virulence, 10(1), 1013-1025 (2019-11-28)
Calcium signaling can elicit different pathways involved in an extreme variety of biological processes. Calcium levels must be tightly regulated in a spatial and temporal manner in order to be efficiently and properly utilized in the host physiology. The Ca2+-ATPase
Y M Zhu et al.
British journal of cancer, 91(11), 1970-1976 (2004-11-17)
Interleukin-8/CXCL8 (IL-8) is a chemokine and angiogenic factor. Recently, IL-8 was identified as an autocrine growth factor in several human cancers. Here, we investigated the expression and function of IL-8 in lung cancer cells. The expressions of IL-8 and its
C Tosh et al.
Acta virologica, 41(3), 153-155 (1997-06-01)
A method of reverse transcription (RT) and polymerase chain reaction (PCR) amplification of 1D (VP1) gene of foot-and-mouth disease (FMD) virus using one reaction mixture containing both avian myeloblastosis virus (AMV) reverse transcriptase (RTase) and Tfl DNA polymerase is described.
Sambrook, J., et al.
Molecular Cloning: A Laboratory Manual, 5-5 (1989)
K Dukas et al.
Analytical biochemistry, 215(1), 66-72 (1993-11-15)
We developed a reverse transcription-polymerase chain reaction (RT-PCR) method which permits the simultaneous amplification of several mRNAs, even though their relative levels may be very different. First-strand cDNAs were synthesized from total RNA by MMLV reverse transcriptase with oligo(dT)15 priming.

商品

Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.

分析基因表达的方法之一是测量基因的mRNA浓度。此类分析面临着若干挑战,例如不同转录本之间的半衰期不同、转录时间模式以及mRNA和蛋白质之间缺乏相关性。

相关内容

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

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