PROS1 anticorps (AA 20-100)

N° du produit ABIN7230792

L’anticorps anti-PROS1 Polyclonal Lapin est utilisé pour la détection de PROS1 dans des échantillons de Humain, Rat et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour PROS1 anticorps (AA 20-100) (ABIN7230792)

Antigène: PROS1 (PROS) (Protein S (PROS))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PROS1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-PROS1 anticorps

Épitope: AA 20-100

Fonction: Rabbit Anti-PROS Polyclonal Antibody

Specificité: The antibody detects endogenous levels of PROS protein

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

Immunogène: Synthesized peptide derived from part region of human PROS protein at AA range: 20-100

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 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: 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 PROS1

Antigène: PROS1 (PROS) (Protein S (PROS))

Autre désignation: PROS

Sujet: Vitamin K-dependent protein SPROS1 encodes a vitamin K-dependent plasma protein that functions as a cofactor for the anticoagulant protease, activated protein C (APC) to inhibit blood coagulation. It is found in plasma in both a free, functionally active form and also in an inactive form complexed with C4b-binding protein. Mutations in PROS1 result in autosomal dominant hereditary thrombophilia. An inactive pseudogene of this locus is located at an adjacent region on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein.

Poids moléculaire: 74kD

ID gène: 5627

UniProt: P07225