USH1G antibody

Catalog No. ABIN7469142

This Rabbit Polyclonal antibody specifically detects USH1G in WB and IHC (p). It exhibits reactivity toward Human.

Quick Overview for USH1G antibody (ABIN7469142)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This USH1G antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-USH1G Antibody

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human USH1G. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: A431

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for USH1G

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

Alternative Name: USH1 protein network component sans

Background:

Synonyms: USH1 protein network component sans , ANKS4A , SANS

Background: This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). [provided by RefSeq]

Molecular Weight: 51 kDa

Gene ID: 124590

UniProt: Q495M9

Pathways: Sensory Perception of Sound