Receptor Accessory Protein 1 antibody (AA 61-110)

Catalog No. ABIN7230988

This Rabbit Polyclonal antibody specifically detects Receptor Accessory Protein 1 in WB and ELISA. It exhibits reactivity toward Mouse and Human.

Quick Overview for Receptor Accessory Protein 1 antibody (AA 61-110) (ABIN7230988)

Target: Receptor Accessory Protein 1 (REEP1)

Reactivity: Mouse, Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Receptor Accessory Protein 1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-Receptor Accessory Protein 1 Antibody

Binding Specificity: AA 61-110

Purpose: Rabbit Anti-REEP1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of REEP1 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 REEP1 protein at AA range: 61-110

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

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 Receptor Accessory Protein 1

Target: Receptor Accessory Protein 1 (REEP1)

Alternative Name: REEP1

Background: Receptor expression-enhancing protein 1, Spastic paraplegia 31 proteinREEP1 encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in REEP1 cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants.

Molecular Weight: 22kD

Gene ID: 65055

UniProt: Q9H902