LOX anticorps (AA 22-168)

N° du produit ABIN2725060

Détail du produit anti-LOX anticorps

Antigène: LOX (Lysyl Oxidase (LOX))

Épitope: AA 22-168

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp LOX est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (IF)

Attributs du produit: Homo sapiens lysyl oxidase (LOX), transcript variant 1

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogène: Human recombinant protein fragment corresponding to amino acids 22-168 of human LOX (NP_002308) produced in HEK293T cell.

Clone: 9G2

Isotype: IgG1

Information d'application

Indications d'application: WB 1:500, IHC 1:150, IF 1:100, FLOW 1:100,

Commentaires:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS ( pH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

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

Détails sur LOX

Antigène: LOX (Lysyl Oxidase (LOX))

Autre désignation: LOX (LOX Produits)

Synonymes: anticorps LOX, anticorps Xlox, anticorps MGC146507, anticorps lox, anticorps zgc:77447, anticorps AI893619, anticorps TSC-160, anticorps H-rev142, anticorps Rrg1, anticorps lysyl oxidase, anticorps lysyl oxidase a, anticorps lysyl oxidase L homeolog, anticorps LOX, anticorps lox, anticorps loxa, anticorps lox.L, anticorps Lox

Sujet: The protein encoded by this gene is an extracellular copper enzyme that initiates the crosslinking of collagens and elastin. The enzyme catalyzes oxidative deamination of the epsilon-amino group in certain lysine and hydroxylysine residues of collagens and lysine residues of elastin. In addition to crosslinking extracellular matrix proteins, the encoded protein may have a role in tumor suppression. Defects in this gene are a cause of autosomal recessive cutis laxa type I (CL type I). Two transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire: 46.8 kDa

ID gène: 4015

NCBI Accession: NM_002317

HGNC: 4015

Pathways: SARS-CoV-2 Protein Interactome