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Rabbit anti-Human PCDH15 Polyclonal Antibody

The antibody against PCDH15 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 160-400 of human PCDH15 (NP_001136235.1) 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-01252A

The antibody against PCDH15 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 160-400 of human PCDH15 (NP_001136235.1) 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-01252A ClonalityPolyclonal
Host SpeciesRabbitTarget NamePCDH15
Target SynonymsUSH1F; CDHR15; DFNB23; PCDH15FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesRat brain, 293T, A-549, Mouse brain, Mouse liver, Mouse spleen, Raji, Rat liver, SH-SY5YApplicationELISA, WB, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 160-400 of human PCDH15 (NP_001136235.1).Target SpeciesHuman
Uniprot IDQ96QU1Immunogen Sequence
Background Information
  • Uniprot Id

    Q96QU1

  • Target Species

    Human

  • Target Name

    PCDH15

  • Target Full Name

    Protocadherin-15

  • Target Function

    Calcium-dependent cell-adhesion protein. Essential for maintenance of normal retinal and cochlear function.

  • Target Involvement

    Usher syndrome 1F (USH1F); Usher syndrome 1D/F (USH1DF); Deafness, autosomal recessive, 23 (DFNB23)

  • Target Subcellular Location

    Cell membrane; Single-pass type I membrane protein.; [Isoform 3]: Secreted.

  • Target Tissue Specificity

    Expressed in brain, lung, kidney, spleen and testis. Found also in the inner and outer synaptic layers, and the nerve fiber layer in adult and fetal retinas. Found in the supporting cells, outer sulcus cells and spiral ganglion of fetal cochlea. Expressed

  • Target Synonyms

    PCDH15; USH1F; Protocadherin-15

  • Target Background

    This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur.

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