Coagulation Factor IX anticorps

N° du produit ABIN951595

Cet anticorps Mouton Polyclonal détecte spécifiquement Coagulation Factor IX dans IHC (p), EIA et ID. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour Coagulation Factor IX anticorps (ABIN951595)

Antigène: Coagulation Factor IX (F9)

Reactivité: Humain

Hôte: Mouton

Clonalité: Polyclonal

Conjugué: Cet anticorp Coagulation Factor IX est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA), Immunodiffusion (ID)

Détail du produit anti-Coagulation Factor IX anticorps

Specificité: Recognizes Human Factor IX as demonstrated by Immunodiffusion. A single positive reactivity band was observed with Normal Human Plasma. No reaction was observed against Factor IX-deficient plasma.

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

Purification: Ammonium Sulfate Precipitation

Immunogène: Human Factor IX purified from plasma.

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Concentration: 10 mg/mL

Buffer: 0.01 M HEPES, pH 7.4, 0.1 M Sodium Chloride and 50 % Glycerol.

Agent conservateur: Azide free

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur Coagulation Factor IX

Antigène: Coagulation Factor IX (F9)

Sujet: Coagulation Factor IX (F9) circulates in the blood as an inactive zymogen. 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 Ca+2 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.Synonyms: Christmas factor, PTC, Plasma thromboplastin component

ID gène: 2158

NCBI Accession: NP_000124