Recombinant人KRT81 protein (ab117016)

概述

  • 产品名称Recombinant人KRT81 protein
  • 蛋白长度Full length protein

描述

  • 性质Recombinant
  • 来源Wheat germ
  • 氨基酸序列
    • AccessionAAH21241
    • 种属Human
    • 序列MKATVIRHGETLRRTKEEINELNRMIQRLTAEVENAKC QNSKLEAAVA QSEQQGEAALSDARCKLAELEGALQKA KQDMACLIREYQEVMNSKLGL DIEIATYRRLLEGEEQR LCEGIGAVNVCVSSSRGGVVCGDLCVSGSRP VTGSV CSAPCNGNVAVSTGLCAPCGQLNTTCGGGSCGVGSC GISSL GVGSCGSSCRKC
    • 分子量48 kDa including tags
    • 氨基酸1 to 202
    • 标签proprietary tag N-Terminus

相关产品

技术指标

Our Abpromise guarantee covers the use of ab117016 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 use within three months from the date of receipt of this protein.
  • 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
    • 1
    • basic
    • ghHb 1
    • ghHb1
    • ghHkb 1
    • ghHKb1
    • hair
    • Hair keratin K2.9
    • Hard keratin type II 1
    • HB 1
    • HB1
    • hHAKB2 1
    • K2.9
    • K81
    • Keratin
    • Keratin 81
    • Keratin hair basic 1
    • Keratin type II cuticular Hb1
    • Keratin-81
    • Keratin81
    • KRT 81
    • KRT81
    • KRT81_HUMAN
    • KRTHB 1
    • KRTHB1
    • Metastatic lymph node 137 gene protein
    • MLN 137
    • MLN137
    • type II cuticular Hb1
    • Type II hair keratin Hb1
    • Type-II keratin Kb21
    see all
  • 组织特异性Abundantly expressed in the differentiating cortex of growing (anagen) hair. Expression is restricted to the keratinocytes of the hair cortex and is absent from inner root sheath and medulla. Expressed in malignant lymph node tissue in breast carcinoma tissue.
  • 疾病相关Defects in KRT81 are a cause of monilethrix (MLTRX) [MIM:158000]. Monilethrix is an autosomal dominant hair disorder characterized clinically by alopecia and follicular papules. Affected hairs have uniform elliptical nodes of normal thickness and intermittent constrictions, internodes at which the hair easily breaks. Usually only the scalp is involved, but in severe forms, the secondary sexual hair, eyebrows, eyelashes, and nails may also be affected.
  • 序列相似性Belongs to the intermediate filament family.
  • Information by UniProt

Recombinant Human KRT81 protein 图像

  • 12.5% SDS-PAGE showing ab117016 at approximately 48.33 kDa.
    Stained with Coomassie Blue.

Recombinant Human KRT81 protein (ab117016)参考文献

ab117016 has not yet been referenced specifically in any publications.

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