PLOD1 anticorps

N° du produit ABIN7263961

Détail du produit anti-PLOD1 anticorps

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PLOD1 est non-conjugé

Application: Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human PLOD1 (NP_000293.2).

Isotype: IgG

Information d'application

Indications d'application: IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 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.

Stock: -20 °C

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

Détails sur PLOD1

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

Autre désignation: PLOD1 (PLOD1 Produits)

Synonymes: anticorps EDS6, anticorps LH, anticorps LH1, anticorps LLH, anticorps PLOD, anticorps Plod, anticorps procollagen-lysine, anticorps 2410042F05Rik, anticorps AI854890, anticorps AV007929, anticorps Lh1, anticorps plod1, anticorps ik:tdsubs_rzpd609-29b19, anticorps plod, anticorps wu:fc29c10, anticorps wu:fc95g08, anticorps wu:fi18a05, anticorps zgc:152876, anticorps procollagen-lysine,2-oxoglutarate 5-dioxygenase 1, anticorps procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1, anticorps procollagen-lysine,2-oxoglutarate 5-dioxygenase 3, anticorps procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 L homeolog, anticorps procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a, anticorps PLOD1, anticorps Plod1, anticorps PLOD3, anticorps plod1.L, anticorps plod1a

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.

ID gène: 5351

UniProt: Q02809