XPA Protein (His tag)
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- Target Alle XPA Proteine anzeigen
- XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
- Protein-Typ
- Recombinant
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Spezies
- Human
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Quelle
- Escherichia coli (E. coli)
- Aufreinigungstag / Konjugat
- Dieses XPA Protein ist gelabelt mit His tag.
- Applikation
- SDS-PAGE (SDS)
- Reinheit
- > 85 % by SDS - PAGE
- Top Product
- Discover our top product XPA Protein
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Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 1-273) protein (GST tag)
XPA Spezies: Human Wirt: Wheat germ Recombinant WB, ELISA, AA, AP
Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 2-273) protein (His tag)Crystallography grade XPA Spezies: Human Wirt: Insektenzellen Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, ELISA, Crys
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- Kommentare
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Synonyms: DNA repair protein complementing XP-A cells, XP1, XPAC
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/ml (determined by Bradford assay)
- Buffer
- 20 mM Tris-HCl buffer (pH 8.0) containing 0.4 M Urea, 10% glycerol
- Lagerung
- 4 °C
- Informationen zur Lagerung
- Avoid repeated freezing and thawing cycles.
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- Target
- XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
- Andere Bezeichnung
- XPA (XPA Produkte)
- Synonyme
- 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
- Hintergrund
- 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.
- Molekulargewicht
- 33.8 kDa (296aa)
- NCBI Accession
- NP_000371
- Pathways
- DNA Reparatur
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