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PCDH15 antibody

PCDH15 Reactivity: Human, Mouse, Rat WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7118101
  • Target See all PCDH15 Antibodies
    PCDH15 (Protocadherin-15 (PCDH15))
    Reactivity
    • 14
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 11
    • 3
    • 2
    Rabbit
    Clonality
    • 14
    • 2
    Polyclonal
    Conjugate
    • 16
    This PCDH15 antibody is un-conjugated
    Application
    • 13
    • 7
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Immunogen affinity purified
    Purity
    ≥95 % as determined by SDS-PAGE
    Immunogen
    PCDH15
    Isotype
    IgG
    Top Product
    Discover our top product PCDH15 Primary Antibody
  • Application Notes
    WB: 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    Expiry Date
    12 months
  • Target
    PCDH15 (Protocadherin-15 (PCDH15))
    Alternative Name
    PCDH15 (PCDH15 Products)
    Synonyms
    CDHR15 antibody, DFNB23 antibody, USH1F antibody, BB078305 antibody, ENSMUSG00000046980 antibody, Gm9815 antibody, Ush1f antibody, av antibody, nmf19 antibody, protocadherin-15 antibody, protocadherin related 15 antibody, protocadherin-15 antibody, protocadherin 15 antibody, PCDH15 antibody, CpipJ_CPIJ005081 antibody, Pcdh15 antibody
    Background
    Synonyms:CDHR15, DFNB23, USH1F, PCD15 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.
    Molecular Weight
    100kDa
    Gene ID
    65217
    UniProt
    Q96QU1
    Pathways
    Sensory Perception of Sound
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