Gpr98 antibody

Catalog No. ABIN7228760

The Rabbit Polyclonal anti-Gpr98 antibody is suitable to detect Gpr98 in samples from Human and Mouse. It has been validated for IHC and IF.

Quick Overview for Gpr98 antibody (ABIN7228760)

Target: Gpr98 (G Protein-Coupled Receptor 98 (Gpr98))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Gpr98 antibody is un-conjugated

Application: Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-Gpr98 Antibody

Purpose: Rabbit Anti-GPR98 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of GPR98 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human GPR98 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC 1:50-300,IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

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

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for Gpr98

Target: Gpr98 (G Protein-Coupled Receptor 98 (Gpr98))

Alternative Name: GPR98

Background: G-protein coupled receptor 98, Monogenic audiogenic seizure susceptibility protein 1 homolog, Usher syndrome type-2C protein, Very large G-protein coupled receptor 1ADGRV1 encodes a member of the G-protein coupled receptor superfamily. The encoded protein contains a 7-transmembrane receptor domain, binds calcium and is expressed in the central nervous system. Mutations in ADGRV1 are associated with Usher syndrome 2 and familial febrile seizures. Several alternatively spliced transcripts have been described.

Molecular Weight: 693kD

Gene ID: 84059

UniProt: Q8WXG9

Pathways: Sensory Perception of Sound