COX4NB anticorps

N° du produit ABIN7234922

Détail du produit anti-COX4NB anticorps

Antigène: COX4NB (COX4 Neighbor (COX4NB))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COX4NB est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human EMC8

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur COX4NB

Antigène: COX4NB (COX4 Neighbor (COX4NB))

Autre désignation: EMC8 (COX4NB Produits)

Synonymes: anticorps COX4NB, anticorps NOC4, anticorps MGC75783, anticorps cox4nb, anticorps fb54g02, anticorps noc4, anticorps wu:fb54g02, anticorps zgc:56331, anticorps C16orf2, anticorps C16orf4, anticorps FAM158B, anticorps Cox4nb, anticorps Fam158b, anticorps Noc4, anticorps ER membrane protein complex subunit 8, anticorps ER membrane protein complex subunit 8 S homeolog, anticorps ER membrane protein complex subunit 9, anticorps EMC8, anticorps emc8, anticorps emc8.S, anticorps EMC9, anticorps Emc8

Sujet: COX4NB (Neighbor of COX4) is a 210 amino acid protein encoded by the human gene COX4NB. COX4NB belongs to the UPF0172 (NOC4) family and is found on chromosome 16, adjacent to the gene that encodes COX4. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other auto-immune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

Poids moléculaire: 24 kDa

UniProt: O43402