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

CDH23 antibody

This anti-CDH23 antibody is a Rabbit Polyclonal antibody detecting CDH23 in ELISA, WB and IHC. Suitable for Human.
Catalog No. ABIN7128859
-15% Promotion 2026
$335.48
$394.68
save $59.20 (-15 %)
Plus shipping costs $50.00
Shipping to: United States
Delivery in 13 to 16 Business Days

Quick Overview for CDH23 antibody (ABIN7128859)

Target

See all CDH23 Antibodies
CDH23 (Cadherin 23 (CDH23))

Reactivity

  • 46
  • 26
  • 19
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 44
  • 1
  • 1
Rabbit

Clonality

  • 46
Polyclonal

Conjugate

  • 18
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CDH23 antibody is un-conjugated

Application

  • 13
  • 13
  • 13
  • 10
  • 8
  • 7
  • 6
  • 3
  • 3
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Purpose

    CDH23 Antibody

    Cross-Reactivity

    Mouse, Rat

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of Human CDH23

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

     pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

    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,-80 °C

    Storage Comment

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    CDH23 (Cadherin 23 (CDH23))

    Alternative Name

    CDH23

    Background

    Background: This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.

    Aliases: CDH23 antibody, KIAA1774 antibody, KIAA1812 antibody, UNQ1894/PRO4340Cadherin-23 antibody, Otocadherin antibody

    UniProt

    Q9H251

    Pathways

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