Thrombomodulin anticorps (AA 500-580)

N° du produit ABIN7224688

Cet anticorps Lapin Polyclonal détecte spécifiquement Thrombomodulin dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour Thrombomodulin anticorps (AA 500-580) (ABIN7224688)

Antigène: Thrombomodulin (THBD)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Thrombomodulin est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Thrombomodulin anticorps

Épitope: AA 500-580

Fonction: Rabbit Anti-CD141 Polyclonal Antibody

Specificité: CD141 Polyclonal Antibody detects endogenous levels of CD141 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the C-terminal region of human CD141 at AA range: 500-580

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,ELISA 1:5000,Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Thrombomodulin

Antigène: Thrombomodulin (THBD)

Autre désignation: CD141

Sujet: THBD, THRM, Thrombomodulin, TM, Fetomodulin, CD antigen CD141The protein encoded by this intronless gene THBD (thrombomodulin) is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in THBD are a cause of thromboembolic disease, also known as inherited thrombophilia.

Poids moléculaire: 100kD

ID gène: 7056

UniProt: P07204