XPA Protein (His tag)
-
- Antigène Voir toutes XPA Protéines
- XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
- Type de proteíne
- Recombinant
-
Origine
- Humain
-
Source
- Escherichia coli (E. coli)
- Purification/Conjugué
- Cette XPA protéine est marqué à la His tag.
- Application
- SDS-PAGE (SDS)
- Pureté
- > 85 % by SDS - PAGE
- Top Product
- Discover our top product XPA Protéine
-
Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 1-273) protein (GST tag)
XPA Origine: Humain Hôte: Wheat germ Recombinant WB, ELISA, AA, AP
Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 2-273) protein (His tag)Crystallography grade XPA Origine: Humain Hôte: Cellules d'insectes Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, ELISA, Crys
-
- Commentaires
-
Synonyms: DNA repair protein complementing XP-A cells, XP1, XPAC
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- 1 mg/ml (determined by Bradford assay)
- Buffer
- 20 mM Tris-HCl buffer (pH 8.0) containing 0.4 M Urea, 10% glycerol
- Stock
- 4 °C
- Stockage commentaire
- Avoid repeated freezing and thawing cycles.
-
- Antigène
- XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
- Autre désignation
- XPA (XPA Produits)
- Synonymes
- CG6358 Protein, DhR14 Protein, DhXPA Protein, DmXPA Protein, Dmel\\CG6358 Protein, Dxpa Protein, EG:EG0007.8 Protein, XPAC Protein, XPA_DROME Protein, Xpa Protein, dmXPA Protein, dxpa Protein, XP1 Protein, AI573865 Protein, Xpac Protein, xpac Protein, xxpa Protein, Xeroderma pigmentosum group A-like Protein, XPA, DNA damage recognition and repair factor Protein, xeroderma pigmentosum, complementation group A Protein, xeroderma pigmentosum, complementation group A L homeolog Protein, Xpac Protein, XPA Protein, Xpa Protein, xpa.L Protein
- Sujet
- 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. Recombinant human XPA protein, fused to His-tag at N-terminus, was expressed in E.coli.
- Poids moléculaire
- 33.8 kDa (296aa)
- NCBI Accession
- NP_000371
- Pathways
- Réparation de l'ADN
-
