CX3CL1 anticorps (AA 40-120)

N° du produit ABIN7227144

Cet anticorps Lapin Polyclonal détecte spécifiquement CX3CL1 dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour CX3CL1 anticorps (AA 40-120) (ABIN7227144)

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

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CX3CL1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CX3CL1 anticorps

Épitope: AA 40-120

Fonction: Rabbit Anti-ABCD3 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of ABCD3 protein

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

Immunogène: Synthesized peptide derived from part region of human ABCD3 protein at AA range: 40-120

Isotype: IgG

Information d'application

Indications d'application: 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

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Date de péremption: 12 months

Détails sur CX3CL1

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

Autre désignation: ABCD3

Sujet: 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.

Poids moléculaire: 72kD

ID gène: 5825

UniProt: P28288

Pathways: Synaptic Membrane