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Merck
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主要文件

安全信息

PLA0195

Sigma-Aldrich

Rabbit anti-MOV10 Antibody, Affinity Purified

Powered by Bethyl Laboratories, Inc.

别名:

MGC2948, Moloney leukemia virus 10, Mov10, Mov10 (Moloney leukemia virus 10, fSAP113, functional spliceosome-associated protein 113, gb110, homolog, homolog (mouse), moloney leukemia virus 10 protein, mouse) homolog

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

rabbit

质量水平

抗体形式

affinity purified immunoglobulin

抗体产品类型

primary antibodies

等级

Powered by Bethyl Laboratories, Inc.

种属反应性

human, mouse

技术

immunoprecipitation (IP): 2-5 μg/mg
western blot: 1:2,000- 1:10,000

登记号

NP_066014.1

UniProt登记号

运输

wet ice

储存温度

2-8°C

靶向翻译后修饰

unmodified

基因信息

rabbit ... MOV10(4343)

免疫原

The epitope recognized by PLA0195 maps to a region between residue 953 and 1003 of human Moloney leukemia virus 10, homolog using the numbering given in entry NP_066014.1 (GeneID 4343).

外形

Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09% Sodium Azide

其他说明

Moloney leukemia virus 10 protein (MOV10) is putative RNA helicase that has been identified as a factor associated with argonaute (Ago) containing complexes. Ago complexes play a central in micro RNA (miRNA) and short-interference RNA (siRNA) silencing.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

12 - Non Combustible Liquids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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分析证书(COA)

Lot/Batch Number

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Julia Kornienko et al.
Nature communications, 14(1), 4312-4312 (2023-07-19)
Severe forms of dilated cardiomyopathy (DCM) are associated with point mutations in the alternative splicing regulator RBM20 that are frequently located in the arginine/serine-rich domain (RS-domain). Such mutations can cause defective splicing and cytoplasmic mislocalization, which leads to the formation
Alessandra Zappulo et al.
Nature communications, 8(1), 583-583 (2017-09-21)
Protein subcellular localization is fundamental to the establishment of the body axis, cell migration, synaptic plasticity, and a vast range of other biological processes. Protein localization occurs through three mechanisms: protein transport, mRNA localization, and local translation. However, the relative

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