Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

PCDH15 antibody

This Rabbit Polyclonal antibody specifically detects PCDH15 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN2463319

Quick Overview for PCDH15 antibody (ABIN2463319)

Target

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

Reactivity

  • 16
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 13
  • 3
  • 3
Rabbit

Clonality

  • 16
  • 3
Polyclonal

Conjugate

  • 19
This PCDH15 antibody is un-conjugated

Application

  • 16
  • 10
  • 6
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Purification

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PCDH15.
  • Application Notes

    PCDH15 antibody can be used for detection of PCDH15 by ELISA at 1:62500. PCDH15 antibody can be used for detection of PCDH15 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handling Advice

    As with any antibody avoid repeat freeze-thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store PCDH15 antibody at -20 °C.
  • Target

    PCDH15 (Protocadherin-15 (PCDH15))

    Alternative Name

    PCDH15

    Background

    PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.

    Molecular Weight

    80 kDa

    Gene ID

    65217

    UniProt

    A2A3E5

    Pathways

    Sensory Perception of Sound
You are here:
Chat with us!