Coagulation Factor IX anticorps

N° du produit ABIN452591

L’anticorps anti-Coagulation Factor IX Monoclonal Souris est utilisé pour la détection de Coagulation Factor IX dans des échantillons de Humain. Il a été validé pour EIA.

Aperçu rapide pour Coagulation Factor IX anticorps (ABIN452591)

Antigène: Coagulation Factor IX (F9)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Coagulation Factor IX est non-conjugé

Application: Enzyme Immunoassay (EIA)

Clone: F9-1

Détail du produit anti-Coagulation Factor IX anticorps

Specificité: Human Factor IX.

Réactivité croisée (Details): Species reactivity (tested):Human.

Attributs du produit: Synonyms: Christmas factor, PTC, Plasma thromboplastin component

Purification: Affinity Chromatography on Protein G.

Immunogène: Human Factor IX.

Isotype: IgG1

Information d'application

Indications d'application: ELISA.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Reconstitution: Restore with Double distillated water to a final concentration of 1.0 mg/mL.

Buffer: 0.01 M PBS, pH 7.2 without preservatives.

Agent conservateur: Without preservative

Stock: -20 °C

Stockage commentaire: Store the antibody (in aliquots) at -20 °C. Avoid repeated freezing and thawing.
Shelf life: one year from despatch.

Date de péremption: 12 months

Détails sur Coagulation Factor IX

Antigène: Coagulation Factor IX (F9)

Sujet: Factor IX circulates in the blood as an inactive zymogen at the normal concentration of approximately 3 μg/mL. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca2+ ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X linked disorder, also called hemophilia B or Christmas disease. The disease affects approximately 1 in 50,000 of the population (almost exclusively males).Synonyms: Christmas factor, PTC, Plasma thromboplastin component

ID gène: 2158

UniProt: P00740