FERMT3 anticorps

N° du produit ABIN7232050

Cet anticorps Lapin Polyclonal détecte spécifiquement FERMT3 dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour FERMT3 anticorps (ABIN7232050)

Antigène: FERMT3 (Fermitin Family Member 3 (FERMT3))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FERMT3 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-FERMT3 anticorps

Fonction: Rabbit Anti-URP2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of URP2 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 URP2 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 FERMT3

Antigène: FERMT3 (Fermitin Family Member 3 (FERMT3))

Autre désignation: URP2

Sujet: Fermitin family homolog 3, Kindlin-3, MIG2-like protein, Unc-112-related protein 2Kindlins are a small family of proteins that mediate protein-protein interactions involved in integrin activation and thereby have a role in cell adhesion, migration, differentiation, and proliferation. The protein encoded by this gene has a key role in the regulation of hemostasis and thrombosis. This protein may also help maintain the membrane skeleton of erythrocytes. Mutations in this gene cause the autosomal recessive leukocyte adhesion deficiency syndrome-III (LAD-III). Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Poids moléculaire: 73kD

ID gène: 83706

UniProt: Q86UX7