X1504
Anti-XPA (N-terminal) 兔抗
~1 mg/mL, affinity isolated antibody, buffered aqueous solution
别名:
Anti-Xeroderma pigmentosum, complementary group A, Anti-XP1, Anti-XPAC
生物来源
rabbit
偶联物
unconjugated
抗体形式
affinity isolated antibody
抗体产品类型
primary antibodies
克隆
polyclonal
表单
buffered aqueous solution
分子量
antigen 35 kDa (doublet)
种属反应性
human
浓度
~1 mg/mL
技术
immunoprecipitation (IP): 5-10 μg using HEK-293T cell lysates
indirect immunofluorescence: 5-10 μg/mL using A549 cells fixed with paraformaldehyde/Triton
western blot: 0.5-1 μg/mL using Jurkat cell lysates
UniProt登记号
运输
dry ice
储存温度
−20°C
基因信息
human ... XPA(7507)
一般描述
XPA (N-terminal), xeroderma pigmentosum, complementation group A, encodes a zinc finger protein involved in DNA excision repair. The encoded protein is part of the NER (nucleotide excision repair) complext which is responsible for repair of UV radiation-i
免疫原
synthetic peptide corresponding to amino acids 15-33 of human XPA, conjugated to KLH via a C-terminal added cysteine residue. The immunizing peptide differs from the rat sequence in three amino acids.
应用
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)
Western Blotting (1 paper)
外形
0.01M 磷酸缓冲盐溶液，pH 7.4，含 15mM 叠氮化钠。
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
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
新产品
此项目有
Iltaeg Cho et al.
PLoS genetics, 9(4), e1003407-e1003407 (2013-05-03)
The Cockayne syndrome complementation group B (CSB) protein is essential for transcription-coupled DNA repair, and mutations in CSB are associated with Cockayne syndrome--a devastating disease with complex clinical features, including the appearance of premature aging, sun sensitivity, and numerous neurological
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