CX3CL1 antibody (AA 40-120)

Catalog No. ABIN7227144

This Rabbit Polyclonal antibody specifically detects CX3CL1 in WB and ELISA. It exhibits reactivity toward Human, Rat and Mouse.

Quick Overview for CX3CL1 antibody (AA 40-120) (ABIN7227144)

Target: CX3CL1 (Chemokine (C-X3-C Motif) Ligand 1 (CX3CL1))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CX3CL1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CX3CL1 Antibody

Binding Specificity: AA 40-120

Purpose: Rabbit Anti-ABCD3 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of ABCD3 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 ABCD3 protein at AA range: 40-120

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 CX3CL1

Target: CX3CL1 (Chemokine (C-X3-C Motif) Ligand 1 (CX3CL1))

Alternative Name: ABCD3

Background: ATP-binding cassette sub-family D member 3, 70 kDa peroxisomal membrane protein, PMP70ABCD3 (ATP Binding Cassette Subfamily D Member 3) is a Protein Coding gene. Diseases associated with ABCD3 include Bile Acid Synthesis Defect, Congenital, 5 and Zellweger Syndrome. Among its related pathways are Nuclear Receptors in Lipid Metabolism and Toxicity and CDK-mediated phosphorylation and removal of Cdc6.

Molecular Weight: 72kD

Gene ID: 5825

UniProt: P28288

Pathways: Synaptic Membrane