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XPC Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT6473
产品名称
XPC Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
XPC XPCC
蛋白名称
XPC
推荐应用
WB
反应种属
Human,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
7508
Human Gene Link
https://www.uniprot.org/uniprot/7508
Human Swissprot No.
Q01831
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q01831/entry
Mouse Gene ID
22591
Mouse Gene Link
https://www.uniprot.org/uniprot/22591
Mouse Swissprot No.
P51612
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/P51612
免疫原
Synthesized peptide derived from human XPC AA range: 395-445
特异性
This antibody detects endogenous levels of XPC at Human/Mouse
稀释度
WB 1:500-2000
参考分子量
103kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a component of the nucleotide excision repair (NER) pathway. There are multiple components involved in the NER pathway, including Xeroderma pigmentosum (XP) A-G and V, Cockayne syndrome (CS) A and B, and trichothiodystrophy (TTD) group A, etc. This component, XPC, plays an important role in the early steps of global genome NER, especially in damage recognition, open complex formation, and repair protein complex formation. Mutations in this gene or some other NER components result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009],
细胞定位
Nucleus . Chromosome . Cytoplasm . Omnipresent in the nucleus and consistently associates with and dissociates from DNA in the absence of DNA damage (PubMed:18682493). Continuously shuttles between the cytoplasm and the nucleus, which is impeded by the presence of NER lesions (PubMed:18682493). .
功能
disease:Defects in XPC are a cause of xeroderma pigmentosum complementation group C (XP-C) [MIM:278720]; also known as xeroderma pigmentosum III (XP3). XP-C is a rare human autosomal recessive disease characterized by solar sensitivity, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities.,function:Involved in DNA excision repair. May play a part in DNA damage recognition and/or in altering chromatin structure to allow access by damage-processing enzymes.,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the XPC family.,subunit:Heterodimer of a 125 kDa subunit (p125) and of a 58 kDa subunit (p58). Interacts with CETN2.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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