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Recombinant Human Melanoma-associated antigen 11 (MAGEA11)

ACP23399

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP23399 Target NameMAGEA11
Target SynonymsMAGEA11; MAGE11Melanoma-associated antigen 11; Cancer/testis antigen 1.11; CT1.11; MAGE-11 antigenFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-429
Protein LengthFull length proteinPurity>85% (SDS-PAGE)
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP43364
Background Information
  • Uniprot Id

    P43364

  • Target Species

    Human

  • Target Name

    MAGEA11

  • Target Full Name

    Melanoma-associated antigen 11

  • Target Function

    Acts as androgen receptor coregulator that increases androgen receptor activity by modulating the receptors interdomain interaction. May play a role in embryonal development and tumor transformation or aspects of tumor progression.

  • Target Subcellular Location

    Nucleus. Cytoplasm.

  • Target Tissue Specificity

    Expressed in tumors of several types, such as melanoma, head and neck squamous cell carcinoma, lung carcinoma and breast carcinoma. Expressed in testis, ovary, prostate, cancerous prostate, breast and adrenal tissue.

  • Target Synonyms

    MAGEA11; MAGE11Melanoma-associated antigen 11; Cancer/testis antigen 1.11; CT1.11; MAGE-11 antigen

  • Target Background

    This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Two transcript variants encoding different isoforms have been found for this gene.

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