Recombinant Human HOXA13 protein (ab114544)

製品の概要

製品の詳細

  • 由来Recombinant
  • 由来Wheat germ
  • アミノ酸配列
    • アクセッション番号P31271
    • 生物種Human
    • 配列DKYMDTAGPAAEEFSSRAKEFAFYHQGYAAGPYHHHQPMPGYLDMPVVPG LGGPGESRHEPLGLPMESYQPWALPNGWNGQMYCPKEQAQPPHLWKSTL
    • 分子量37 kDa including tags
    • 領域208 to 306

特性

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.

  • アプリケーション

    ELISA

    Western blot

    SDS-PAGE

  • 製品の状態Liquid
  • 備考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...

前処理および保存

  • 保存方法および安定性

    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

関連情報

  • 別名
    • 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
  • 機能Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.
  • 関連疾患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.
  • 配列類似性Belongs to the Abd-B homeobox family.
    Contains 1 homeobox DNA-binding domain.
  • 細胞内局在Nucleus.
  • Information by UniProt

Recombinant Human HOXA13 protein 画像

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

Recombinant Human HOXA13 protein (ab114544) 使用論文

ab114544 has not yet been referenced specifically in any publications.

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