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一般描述
莫洛尼鼠白血病病毒(M-MLV)逆转录酶从质粒表达M-MLV部分pol基因的大肠杆菌中分离获得。MoMLVRT由671个氨基酸组成。它是一种DNA聚合酶，可通过单链RNA、DNA或RNA-DNA杂合体（使用引物）合成互补的DNA链。
应用
M-MLV逆转录酶已用于：
- 制备cDNA文库或合成第一条cDNA链
- 2步法RT-PCR检测
- 实时定量聚合酶链反应(RT-qPCR)
- 逆转录
特点和优势
- 热稳定性逆转录酶在37℃时活性佳。
- 可用于制备长达7 kb的第一链cDNA。
包装
本品为含DTT 的10× M-MLV逆转录酶缓冲液。
单位定义
一单位本品可在10分钟内将1 nmol TTP整合进酸性可沉淀物质中。反应在37℃下进行，以poly(A)：oligo dT为模板：引物。
制备说明
该酶从可在质粒上表达M-MLV pol基因的Escherichia coli 中纯化所得。
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.
警示用语：
Danger
危险声明
预防措施声明
危险分类
Resp. Sens. 1
储存分类代码
12 - Non 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
Murine leukemia virus reverse transcriptase: structural comparison with HIV-1 reverse transcriptase
Cote ML and Roth MJ
Virus Research, 134, 186-202 (2008)
Frost hardiness expression and characterisation in wheat at ear emergence
Al IM, et al.
Journal of agronomy and crop science, 199, 66-74 (2013)
Functional analysis of LHCSR1, a protein catalyzing NPQ in mosses, by heterologous expression in Arabidopsis thaliana
Dikaios I, et al.
Photosynthesis Research, 142, 249-264 (2019)
Downregulation of the PHLDA1 gene in IMR-32 neuroblastoma cells increases levels of Aurora A, TRKB and affects proteins involved in apoptosis and autophagy pathways
Durbas M, et al.
International Journal of Oncology, 49(2), 823-837 (2016)
Downregulation of the PHLDA1 gene in IMR-32 neuroblastoma cells increases levels of Aurora A, TRKB and affects proteins involved in apoptosis and autophagy pathways
Durbas M, et al.
International Journal of Oncology, 49, 823-837 (2016)
商品
Small interfering RNAs (siRNAs) are powerful tools for gene expression knockdown, widely used in molecular biology.
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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