Search results for Cadherin Related 23 (CDH23) Antibody

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Cadherin Related 23 (CDH23) Antibody Brand Logo
ID: BAB948694278

Cadherin Related 23 (CDH23) Antibody, Abbexa, abx013920

Rabbit polyclonal antibody against CDH23 protein. Immunogen region is N-terminal.

Host

Rabbit

Reactivity

Human, Mouse, Rat

Applications

ELISA, IF/ICC

Conjugation

Unconjugated

Cadherin Related 23 (CDH23) Antibody Brand Logo
ID: BAB836559393

Cadherin Related 23 (CDH23) Antibody, Abbexa, abx430494

CDH23 Antibody is a Goat Polyclonal antibody against CDH23.

Host

Goat

Reactivity

Human

Applications

P-ELISA, WB

Conjugation

Unconjugated

Cadherin Related 23 (CDH23) Antibody Brand Logo
ID: BAB741503662

Cadherin Related 23 (CDH23) Antibody, Abbexa, abx231548

CDH23 Antibody is a Rabbit Polyclonal against CDH23.

Host

Rabbit

Reactivity

Human, Mouse, Rat

Applications

ELISA, WB, IHC

Conjugation

Unconjugated

Cadherin Related 23 (CDH23) Antibody Brand Logo
ID: BAB542755429

Cadherin Related 23 (CDH23) Antibody, Abbexa, abx003739

CDH23 Antibody is a Rabbit Polyclonal antibody against CDH23. 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. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described.

Host

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB

Conjugation

Unconjugated

Cadherin Related 23 (CDH23) Antibody Brand Logo
ID: BAB531206033

Cadherin Related 23 (CDH23) Antibody, Abbexa, abx002090

CDH23 Antibody is a Rabbit Polyclonal antibody against CDH23. 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.

Host

Rabbit

Reactivity

Human, Mouse

Applications

ELISA, WB, IHC

Conjugation

Unconjugated

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