XPA Protein (AA 1-273) (His tag)
Aperçu rapide pour XPA Protein (AA 1-273) (His tag) (ABIN1098757)
Antigène
Voir toutes XPA ProtéinesType de proteíne
Origine
Source
Application
Pureté
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Attributs du protein
- AA 1-273
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Purification/Conjugué
- Cette XPA protéine est marqué à la His tag.
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Séquence
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MAAADGA LPEAAALEQP AELPASVRAS IERKRQRALM LRQARLAARP YSATAAAATG GMANVKAAPK IIDTGGGFIL EEEEEEEQKI GKVVHQPGPV MEFDYVICEE CGKEFMDSYL MNHFDLPTCD NCRDADDKHK LITKTEAKQE YLLKDCDLEK REPPLKFIVK KNPHHSQWGD MKLYLKLQIV KRSLEVWGSQ EALEEAKEVR QENREKMKQK KFDKKVKELR RAVRSSVWKR ETIVHQHEYG PEENLEDDMY RKTCTMCGHE LTYEKM -
Purification
- > 85% by SDS-PAGE
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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Synonyms: DNA repair protein complementing XP-A cells, XP1, XPAC
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- 20 mM Tris-HCl buffer ( pH 8.0) containing 0.4M urea, 10 % glycerol
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Stock
- 4 °C,-20 °C,-80 °C
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Stockage commentaire
- Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
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- XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
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Autre désignation
- XPA
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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.
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Poids moléculaire
- 33.8 kDa (296aa)
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NCBI Accession
- NP_000371
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Pathways
- Réparation de l'ADN
Antigène
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