XPA Antibody (Clone AT37C5)

XPA, also known as DNA repair protein complementing XP-A cells, belongs 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.
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Properties

Data Sheet Click for Datasheet
Catalog Number MA01376
Size 100 µL
Host Type Mouse
Immunogen Recombinant human XPA (1-273aa) purified from E. coli
Specificity
Isotype IgG3, k
Reacitivity Human
Clone Anti-human XPA mAb, clone AT37C5, is derived from hybridization of mouse F0 myeloma cells with spleen cells from BALB/c mice immunized with a recombinant human XPA protein.
Uniprot
Concentration 1 mg/ml
Dilution
Formulation Liquid. In Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% Glycerol.
Application ELISA, WB.
Other Names DNA repair protein complementing XP-A cells, XP1, XPAC.
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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