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Merck

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

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

rabbit

品質等級

抗體表格

affinity purified immunoglobulin

抗體產品種類

primary antibodies

等級

Powered by Bethyl Laboratories, Inc.

物種活性

human, mouse

技術

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

登錄號

NP_066014.1

UniProt登錄號

運輸包裝

wet ice

儲存溫度

2-8°C

目標翻譯後修改

unmodified

基因資訊

rabbit ... MOV10(4343)

相关类别

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).

外觀

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

其他說明

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.

免責聲明

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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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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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