PROZ anticorps (Cy7)

N° du produit ABIN1421030

L’anticorps anti-PROZ Polyclonal Lapin est utilisé pour la détection de PROZ dans des échantillons de Humain. Il a été validé pour IF.

Aperçu rapide pour PROZ anticorps (Cy7) (ABIN1421030)

Antigène: PROZ (Protein Z, Vitamin K-Dependent Plasma Glycoprotein (PROZ))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PROZ est conjugé à/à la Cy7

Application: Immunofluorescence (IF)

Détail du produit anti-PROZ anticorps (Cy7)

Fonction: Protein Z Polyclonal Antibody, Cy7 Conjugated

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human Protein Z

Isotype: IgG

Information d'application

Indications d'application: IF()

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur PROZ

Antigène: PROZ (Protein Z, Vitamin K-Dependent Plasma Glycoprotein (PROZ))

Autre désignation: Protein Z

Sujet:

Synonyms: Protein Z, vitamin K dependent plasma glycoprotein, PROZ, PROZ_HUMAN, PZ antibody Vitamin K-dependent protein Z.

Background: This gene encodes a liver vitamin K-dependent glycoprotein that is synthesized in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012].

ID gène: 8858