Human XPA antibody
XPA, also known as DNA repair protein complementing XP-A cells, belong to the XPA family. This protein is involved in DNA excision repair. It Initiates repair by binding to damaged sites with various affinities, depending on the photoproduct and the transcriptional state of the region. Defects in XPA are a cause of xeroderma pigmentosum complementation group A (XP-A), which 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.
Product Specifications
Product Name Alternative
DNA repair protein complementing XP-A cells, XP1, XPAC
Host
Mouse
Antigen Species
Human
Reactivity
Human
Immunogen
Recombinant human XPA (1-273aa) purified from E. coli
Clonality
Monoclonal
Isotype
IgG1 κ
Clone
AT71H3
Conjugation
Unconjugated
Applications
ELISA, WB, ICC/IF
Purification Method
By protein-A affinity chromatography
Concentration
1 mg/mL (determined by BCA assay)
Additionnal Information
References & Citations
Pan Y.R., et al. (2009) Cell Cycle 8:655-664.; ; James, et al. (2005) Andrews Diseases of the Skin: Clinical Dermatology. (10th ed.) . Saunders.
Storage Conditions
Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
Formulation
Liquid in. Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycerol
Applications Notes
Scientific Category
Epigenomics (Transcription & Translation)
NCBI Accession Number
NP_000371
Uniprot Accession Number
P23025
WB Description
IF Description
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