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: REEP1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of REEP1 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: 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.

Target Details for Receptor Accessory Protein 1

Target: Receptor Accessory Protein 1 (REEP1)

Alternative Name: REEP1

Background: Rabbit Anti-REEP1 Polyclonal Antibody,Receptor expression-enhancing protein 1, Spastic paraplegia 31 protein,REEP1 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.,REEP1

Molecular Weight: observerd band 22kDa

Gene ID: 65055

UniProt: Q9H902