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Rabbit anti-Human COCH Polyclonal Antibody

The antibody against COCH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 20-260 of human COCH (NP_001128530.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on IHC-P, IF/ICC, ELISA.

ADA-02962A

The antibody against COCH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 20-260 of human COCH (NP_001128530.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on IHC-P, IF/ICC, ELISA.

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Specifications


Cat.No ADA-02962A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCOCH
Target SynonymsDFNA9; COCH5B2; DFNB110; COCH-5B2; COCHFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
ApplicationELISA, IF/ICC, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 20-260 of human COCH (NP_001128530.1).Target SpeciesHuman
Uniprot IDO43405Immunogen Sequence
Background Information
  • Uniprot Id

    O43405

  • Target Species

    Human

  • Target Name

    COCH

  • Target Full Name

    Cochlin

  • Target Function

    Plays a role in the control of cell shape and motility in the trabecular meshwork.

  • Target Involvement

    Deafness, autosomal dominant, 9 (DFNA9)

  • Target Subcellular Location

    Secreted, extracellular space, extracellular matrix.

  • Target Tissue Specificity

    Expressed in inner ear structures; the cochlea and the vestibule.

  • Target Synonyms

    COCH; COCH5B2; UNQ257/PRO294Cochlin; COCH-5B2

  • Target Background

    The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94% and 79% amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated.

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