Coagulation Factor IX anticorps (AA 266-295)

N° du produit ABIN1538212

Cet anticorps Lapin Polyclonal détecte spécifiquement Coagulation Factor IX dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour Coagulation Factor IX anticorps (AA 266-295) (ABIN1538212)

Antigène: Coagulation Factor IX (F9)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Coagulation Factor IX est non-conjugé

Application: Western Blotting (WB)

Clone: RB36658

Détail du produit anti-Coagulation Factor IX anticorps

Épitope: AA 266-295

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This F9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 266-295 amino acids from the Central region of human F9.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:2000. WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: F9 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur Coagulation Factor IX

Antigène: Coagulation Factor IX (F9)

Autre désignation: F9

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.

Poids moléculaire: 51778

ID gène: 2158

NCBI Accession: NP_000124

UniProt: P00740