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PCDH15 antibody (AA 160-400)

This anti-PCDH15 antibody is a Rabbit Polyclonal antibody detecting PCDH15 in WB and IHC. Suitable for Human.
Catalog No. ABIN6145289

Quick Overview for PCDH15 antibody (AA 160-400) (ABIN6145289)

Target

See all PCDH15 Antibodies
PCDH15 (Protocadherin-15 (PCDH15))

Reactivity

  • 15
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 12
  • 3
  • 3
Rabbit

Clonality

  • 15
  • 3
Polyclonal

Conjugate

  • 18
This PCDH15 antibody is un-conjugated

Application

  • 15
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  • 6
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  • 2
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  • 1
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Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 160-400

    Sequence

    TVNELTPVGT TIFTGFSGDN GATDIDDGPN GQIEYVIQYN PDDPTSNDTF EIPLMLTGNI VLRKRLNYED KTRYFVIIQA NDRAQNLNER RTTTTTLTVD VLDGDDLGPM FLPCVLVPNT RDCRPLTYQA AIPELRTPEE LNPIIVTPPI QAIDQDRNIQ PPSDRPGILY SILVGTPEDY PRFFHMHPRT AELSLLEPVN RDFHQKFDLV IKAEQDNGHP LPAFAGLHIE ILDENNQSPY F

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 160-400 of human PCDH15 (NP_001136235.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:100 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    PCDH15 (Protocadherin-15 (PCDH15))

    Alternative Name

    PCDH15

    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.,PCDH15,CDHR15,DFNB23,USH1F,PCDH15

    Molecular Weight

    92 kDa/106 kDa/185 kDa/197 kDa/216 kDa

    Gene ID

    65217

    UniProt

    Q96QU1

    Pathways

    Sensory Perception of Sound
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