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Rabbit anti-Human ESPN Polyclonal Antibody

The antibody against ESPN was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 585-854 of human ESPN (NP_113663.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

ADA-04753A

The antibody against ESPN was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 585-854 of human ESPN (NP_113663.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

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Specifications


Cat.No ADA-04753A ClonalityPolyclonal
Host SpeciesRabbitTarget NameESPN
Target SynonymsUSH1M; DFNB36; LP2654; ESPNFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse testis, Rat testisApplicationELISA, WB, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 585-854 of human ESPN (NP_113663.2).Target SpeciesHuman
Uniprot IDB1AK53Immunogen Sequence
Background Information
  • Uniprot Id

    B1AK53

  • Target Species

    Human

  • Target Name

    ESPN

  • Target Full Name

    Espin

  • Target Function

    Multifunctional actin-bundling protein. Plays a major role in regulating the organization, dimension, dynamics and signaling capacities of the actin filament-rich microvilli in the mechanosensory and chemosensory cells. Required for the assembly and stabilization of the stereociliary parallel actin bundles. Plays a crucial role in the formation and maintenance of inner ear hair cell stereocilia. Involved in the elongation of actin in stereocilia. In extrastriolar hair cells, required for targeting MYO3B to stereocilia tips, and for regulation of stereocilia diameter and staircase formation.

  • Target Involvement

    Deafness, autosomal recessive, 36, with or without vestibular involvement (DFNB36)

  • Target Subcellular Location

    Cytoplasm, cytoskeleton. Cell projection, stereocilium. Cell projection, microvillus.

  • Target Synonyms

    ESPN; DFNB36; LP2654Espin; Autosomal recessive deafness type 36 protein; Ectoplasmic specialization protein

  • Target Background

    This gene encodes a multifunctional actin-bundling protein. It plays a major role in regulating the organization, dimensions, dynamics, and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in various mechanosensory and chemosensory cells. Mutations in this gene are associated with autosomal recessive neurosensory deafness, and autosomal dominant sensorineural deafness without vestibular involvement.

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