USH1G antibody (AA 1-300)

Catalog No. ABIN7175154

Product Details anti-USH1G Antibody

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

Binding Specificity: AA 1-300

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This USH1G antibody is un-conjugated

Application: ELISA

Cross-Reactivity: Human

Purification: >95%, Protein G purified

Immunogen: Recombinant Human Usher syndrome type-1G protein (1-300AA)

Isotype: IgG

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Preservative: 0.03 % Proclin 300
Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

Preservative: ProClin

Precaution of Use: This product contains ProClin: 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 Details for USH1G

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

Alternative Name: USH1G (USH1G Products)

Background:

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.

Aliases: ANKS 4A antibody, ANKS4A antibody, FLJ33924 antibody, SANS antibody, Scaffold protein containing ankyrin repeats and SAM domain antibody, USH 1G antibody, USH1G antibody, USH1G_HUMAN antibody, Usher syndrome 1G (autosomal recessive) antibody, Usher syndrome type 1G protein antibody, Usher syndrome type-1G protein antibody

UniProt: Q495M9

Pathways: Sensory Perception of Sound