CABP4 antibody

Catalog No. ABIN7227560

The Rabbit Polyclonal anti-CABP4 antibody is suitable to detect CABP4 in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for CABP4 antibody (ABIN7227560)

Target: CABP4 (Calcium Binding Protein 4 (CABP4))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CABP4 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CABP4 Antibody

Purpose: Rabbit Anti-CABP4 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of CABP4 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 CABP4 protein

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 CABP4

Target: CABP4 (Calcium Binding Protein 4 (CABP4))

Alternative Name: CABP4

Background: Calcium-binding protein 4, CaBP4CABP4 (Calcium Binding Protein 4) is a Protein Coding gene. Diseases associated with CABP4 include Cone-Rod Synaptic Disorder, Congenital Nonprogressive and Congenital Stationary Night Blindness, Type 2B. Among its related pathways are Visual Cycle in Retinal Rods. CABP4 encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in CABP4 are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for CABP4.

Molecular Weight: 30kD

Gene ID: 57010

UniProt: P57796