Recombinant人HOXA13 protein (ab114544)

概述

描述

  • 性质Recombinant
  • 来源Wheat germ
  • 氨基酸序列
    • AccessionP31271
    • 种属Human
    • 序列DKYMDTAGPAAEEFSSRAKEFAFYHQGYAAGPYHHHQPMPGYLDMPVVPG LGGPGESRHEPLGLPMESYQPWALPNGWNGQMYCPKEQAQPPHLWKSTL
    • 分子量37 kDa including tags
    • 氨基酸208 to 306

技术指标

Our Abpromise guarantee covers the use of ab114544 in the following tested applications.

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

  • 应用

    ELISA

    Western blot

    SDS-PAGE

  • 形式Liquid
  • 补充说明Protein concentration is above or equal to 0.05 mg/ml.
    This protein is 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: 0.79% Tris HCl, 0.3% Glutathione

常规信息

  • 别名
    • Homeo box 1J
    • Homeo box A13
    • Homeobox 1J
    • Homeobox A13
    • Homeobox protein Hox A13
    • Homeobox protein Hox-1J
    • Homeobox protein Hox-A13
    • Homeobox protein HOXA13
    • Homeobox1J
    • HomeoboxA13
    • HOX 1
    • HOX 1J
    • Hox 1J protein
    • HOX A13
    • HOX1
    • HOX1J
    • HOXA 13
    • HOXA13
    • HXA13_HUMAN
    • Transcription factor HOXA13
    see all
  • 功能Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.
  • 疾病相关Defects in HOXA13 are the cause of hand-foot-genital syndrome (HFGS) [MIM:140000]; also known as hand-foot-uterus syndrome. The clinical features include small feet with unusually short great toes and abnormal thumbs. Females with the disorder have duplication of the genital tract.
    Defects in HOXA13 are the cause of Guttmacher syndrome (GUTTS) [MIM:176305]. Guttmacher syndrome is a dominantly inherited combination of distal limb and genital tract abnormalities. It has several features in common with hand-foot-genital syndrome, including hypoplastic first digits and hypospadias. Typical features not seen in hand-foot-genital syndrome include postaxial polydactyly of the hands and uniphalangeal second toes with absent nails.
  • 序列相似性Belongs to the Abd-B homeobox family.
    Contains 1 homeobox DNA-binding domain.
  • 细胞定位Nucleus.
  • Information by UniProt

Recombinant Human HOXA13 protein 图像

  • 12.5% SDS-PAGE Stained with Coomassie Blue showing ab114544.

Recombinant Human HOXA13 protein (ab114544)参考文献

ab114544 has not yet been referenced specifically in any publications.

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