Coagulation Factor IX anticorps

N° du produit ABIN7258664

Détail du produit anti-Coagulation Factor IX anticorps

Antigène: Coagulation Factor IX (F9)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Coagulation Factor IX est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human Factor IX / F9 (NP_000124.1).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 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 Coagulation Factor IX

Antigène: Coagulation Factor IX (F9)

Autre désignation: Factor IX / F9 (F9 Produits)

Synonymes: anticorps AA407498, anticorps AI506714, anticorps AK-3, anticorps Ak3l, anticorps Ak3l1, anticorps Akl3l, anticorps FIX, anticorps HEMB, anticorps P19, anticorps PTC, anticorps THPH8, anticorps AW111646, anticorps Cf-9, anticorps Cf9, anticorps f9, anticorps zgc:109775, anticorps fix, anticorps ptc, anticorps hemb, anticorps FIXA, anticorps zgc:136807, anticorps adenylate kinase 3, anticorps coagulation factor IX, anticorps coagulation factor IXa, anticorps coagulation factor 9, anticorps coagulation factor 9 S homeolog, anticorps Coagulation factor IX, anticorps coagulation factor IXb, anticorps Ak3, anticorps F9, anticorps f9a, anticorps f9, anticorps CpipJ_CPIJ003776, anticorps CpipJ_CPIJ009129, anticorps CpipJ_CPIJ013063, anticorps CpipJ_CPIJ013624, anticorps Tsp_01441, anticorps f9.S, anticorps fa9, anticorps f9b

Sujet: This gene encodes vitamin K-dependent coagulation factor IX that 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. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.

Poids moléculaire:

Observed_MW: 50 kDa

Calculated_MW: 47 kDa/51 kDa

ID gène: 2158

UniProt: P00740