Recombinant人ERCC8 protein (ab114805)

概述

描述

  • 性质Recombinant
  • 来源Wheat germ
  • 氨基酸序列
    • AccessionQ13216
    • 种属Human
    • 序列MLGFLSARQTGLEDPLRLRRAESTRRVLGLELNKDRDVERIHGGGINTLD IEPVEGRYMLSGGSDGVIVLYDLENSSRQSYYTCKAVCSIGRDHPDVHRY SVETVQWYPHDTGMFTSSSFDKTLKVWDTNTLQTADVFNFEETVYSHHMS PVSTKHCLVAVGTRGPKVQLCDLKSGSCSHILQGHRQEILAVSWSPRYDY ILATASADSRVKLWDVRRASGCLITLDQHNGKKSQAVESANTAHNGKVNG LCFTSDGLHLLTVGTDNRMRLWNSSNGENTLVNYGKVCNNSKKGLKFTVS CGCSSEFVFVPYGSTIAVYTVYSGEQITMLKGHYKTVDCCVFQSNFQELY SGSRDCNILAWVPSLYEPVPDDDETTTKSQLNPAFEDAWSSSDEEG
    • 分子量70 kDa including tags
    • 氨基酸1 to 396

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技术指标

Our Abpromise guarantee covers the use of ab114805 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • 应用

    Western blot

    SDS-PAGE

    ELISA

  • 形式Liquid
  • 补充说明Protein concentration is above or equal to 0.05 mg/ml.
    Best used within three months from the date of receipt.
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

常规信息

  • 别名
    • CKN1
    • Cockayne syndrome type A
    • Cockayne syndrome WD repeat protein CSA
    • CSA
    • DNA excision repair protein ERCC-8
    • DNA excision repair protein ERCC8
    • ERCC 8
    • ERCC8
    • ERCC8_HUMAN
    • excision repair cross-complementing rodent repair deficiency, complementation group 8
    see all
  • 功能Substrate-recognition component of the CSA complex, a DCX (DDB1-CUL4-X-box) E3 ubiquitin-protein ligase complex, involved in transcription-coupled nucleotide excision repair. The CSA complex (DCX(ERCC8) complex) promotes the ubiquitination and subsequent proteasomal degradation of ERCC6 in a UV-dependent manner; ERCC6 degradation is essential for the recovery of RNA synthesis after transcription-coupled repair. It is required for the recruitement of XAB2, HMGN1 and TCEA1/TFIIS to a transcription-coupled repair complex which removes RNA polymerase II-blocking lesions from the transcribed strand of active genes.
  • 通路Protein modification; protein ubiquitination.
  • 疾病相关Defects in ERCC8 are the cause of Cockayne syndrome type A (CSA) [MIM:216400]. Cockayne syndrome is a rare disorder characterized by cutaneous sensitivity to sunlight, abnormal and slow growth, cachectic dwarfism, progeroid appearance, progressive pigmentary retinopathy and sensorineural deafness. There is delayed neural development and severe progressive neurologic degeneration resulting in mental retardation. Two clinical forms are recognized: in the classical form or Cockayne syndrome type 1, the symptoms are progressive and typically become apparent within the first few years or life; the less common Cockayne syndrome type 2 is characterized by more severe symptoms that manifest prenatally. Cockayne syndrome shows some overlap with certain forms of xeroderma pigmentosum. Unlike xeroderma pigmentosum, patients with Cockayne syndrome do not manifest increased freckling and other pigmentation abnormalities in the skin and have no significant increase in skin cancer.
  • 序列相似性Contains 5 WD repeats.
  • 细胞定位Nucleus.
  • Information by UniProt

Recombinant Human ERCC8 protein 图像

  • ab114805 on 12.5% SDS-PAGE Stained with Coomassie Blue.

Recombinant Human ERCC8 protein (ab114805)参考文献

ab114805 has not yet been referenced specifically in any publications.

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