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Rabbit anti-Human AMH/MIS Monoclonal Antibody

The antibody against AMH/MIS was raised in Rabbit using the recombinant protein of human AMH/MIS as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on IHC-P, ELISA.

ADA-14536A

The antibody against AMH/MIS was raised in Rabbit using the recombinant protein of human AMH/MIS as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on IHC-P, ELISA.

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Specifications


Cat.No ADA-14536A ClonalityMonoclonal
Host SpeciesRabbitTarget NameAMH/MIS
Target SynonymsMIF; MIS; AMH/MISFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
ApplicationELISA, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant protein of human AMH/MIS.Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP03971
Background Information
  • Uniprot Id

    P03971

  • Target Species

    Human

  • Target Name

    AMH

  • Target Full Name

    Muellerian-inhibiting factor

  • Target Function

    This glycoprotein, produced by the Sertoli cells of the testis, causes regression of the Muellerian duct. It is also able to inhibit the growth of tumors derived from tissues of Muellerian duct origin.

  • Target Involvement

    Persistent Muellerian duct syndrome 1 (PMDS1)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    TGF-beta family

  • Target Synonyms

    MIF; MIS; AMH

  • Target Background

    This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate N- and C-terminal cleavage products that homodimerize and associate to form a biologically active noncovalent complex. This complex binds to the anti-Mullerian hormone receptor type 2 and causes the regression of Mullerian ducts in the male embryo that would otherwise differentiate into the uterus and fallopian tubes. This protein also plays a role in Leydig cell differentiation and function and follicular development in adult females. Mutations in this gene result in persistent Mullerian duct syndrome.

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