USH1G antibody

Catalog No. ABIN5705181

Product Details anti-USH1G Antibody

Target: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This USH1G antibody is un-conjugated

Application: ELISA, Immunoprecipitation (IP)

Immunogen: Usher syndrome 1G (autosomal recessive)

Isotype: IgG

Application Details

Application Notes: IP:1:200-1:2000

Restrictions: For Research Use only

Handling

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.

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Expiry Date: 12 months

Target Details for USH1G

Target: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Alternative Name: USH1G (USH1G Products)

Synonyms: ANKS4A antibody, SANS antibody, Sans antibody, js antibody, USH1 protein network component sans antibody, USH1G antibody, Ush1g antibody

Background: Synonyms:ANKS4A, FLJ33924, SANS, USH1G, Usher syndrome type 1G protein Background:Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.

Molecular Weight: 40kDa

Gene ID: 124590

UniProt: Q495M9

Pathways: Sensory Perception of Sound