VWA1 anticorps

N° du produit ABIN7232128

Cet anticorps Lapin Polyclonal détecte spécifiquement VWA1 dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour VWA1 anticorps (ABIN7232128)

Antigène: VWA1 (Von Willebrand Factor A Domain Containing 1 (VWA1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp VWA1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-VWA1 anticorps

Fonction: Rabbit Anti-VWA1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of VWA1 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 VWA1 protein

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 VWA1

Antigène: VWA1 (Von Willebrand Factor A Domain Containing 1 (VWA1))

Autre désignation: VWA1

Sujet: Von Willebrand factor A domain-containing protein 1VWA1 belongs to the von Willebrand factor (VWF, MIM 613160) A (VWFA) domain superfamily of extracellular matrix proteins and appears to play a role in cartilage structure and function. VWA1 (Von Willebrand Factor A Domain Containing 1) is a Protein Coding gene. Diseases associated with VWA1 include Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant and Acrofacial Dysostosis 1, Nager Type.

Poids moléculaire: 48kD

ID gène: 64856

UniProt: Q6PCB0