LOXL1 anticorps

N° du produit ABIN7115988

Cet anticorps anti-LOXL1 est un anticorps Lapin Polyclonal détectant LOXL1 dans WB et ELISA. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour LOXL1 anticorps (ABIN7115988)

Antigène: LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LOXL1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-LOXL1 anticorps

Fonction: LOXL1 antibody

Purification: Immunogen affinity purified

Pureté: ≥95 % as determined by SDS-PAGE

Immunogène: lysyl oxidase-like 1

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur LOXL1

Antigène: LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

Autre désignation: LOXL1

Sujet:

Synonyms: Lysyl oxidase homolog 1|Lysyl oxidase-like protein 1 (LOL)|LOXL1|LOXL

Background: This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome.

Poids moléculaire: 70 kDa

ID gène: 4016

UniProt: Q08397