USH1G antibody

Catalog No. ABIN7120659

This anti-USH1G antibody is a Rabbit Polyclonal antibody detecting USH1G in ELISA and IP. Suitable for Human.

Quick Overview for USH1G antibody (ABIN7120659)

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)

Product Details anti-USH1G Antibody

Purification: Immunogen affinity purified

Purity: ≥95 % as determined by SDS-PAGE

Immunogen: Usher syndrome 1G(autosomal recessive)

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

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.

Storage: -20 °C

Storage Comment: -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

Expiry Date: 12 months

Target Details for USH1G

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

Alternative Name: USH1G

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: 52 kDa

Gene ID: 124590

UniProt: Q495M9

Pathways: Sensory Perception of Sound