PLOD1 anticorps (AA 23-640)

N° du produit ABIN7872549

L’anticorps anti-PLOD1 Polyclonal Lapin est utilisé pour la détection de PLOD1 dans des échantillons de Humain. Il a été validé pour WB et ELISA.

Aperçu rapide pour PLOD1 anticorps (AA 23-640) (ABIN7872549)

Antigène: PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PLOD1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-PLOD1 anticorps

Épitope: AA 23-640

Fonction: PLOD1 Antibody / Lysyl hydroxylase 1 / LH1

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (amino acids K23-A640) was used as the immunogen for the PLOD1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the PLOD1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the PLOD1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur PLOD1

Antigène: PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))

Autre désignation: PLOD1

Sujet: Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. Two transcript variants encoding different isoforms have been found for this gene.

UniProt: Q02809