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
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
antigen 35 kDa (doublet)
species reactivity
human
concentration
~1 mg/mL
technique(s)
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 accession no.
shipped in
dry ice
storage temp.
−20°C
Gene Information
human ... XPA(7507)
General description
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
Immunogen
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.
Application
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)
Physical form
0.01M 磷酸缓冲盐溶液，pH 7.4，含 15mM 叠氮化钠。
Disclaimer
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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存储类别
12 - Non Combustible Liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
相关内容
Instructions
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