STRA6 anticorps (AA 151-250) (Cy7)

N° du produit ABIN1708370

L’anticorps Lapin Polyclonal anti-STRA6 a été validé pour IF (cc) et IF (p). Il convient pour détecter STRA6 dans des échantillons de Humain.

Aperçu rapide pour STRA6 anticorps (AA 151-250) (Cy7) (ABIN1708370)

Antigène: STRA6 (Stimulated By Retinoic Acid 6 (STRA6))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp STRA6 est conjugé à/à la Cy7

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-STRA6 anticorps (Cy7)

Épitope: AA 151-250

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human STRA6

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur STRA6

Antigène: STRA6 (Stimulated By Retinoic Acid 6 (STRA6))

Autre désignation: STRA6

Sujet:

Synonyms: Stimulated by retinoic acid gene 6 protein homolog, STRA6_HUMAN.

Background: STRA6 is a 667 amino acid, multi-pass cell membrane protein. Stra6 functions as a cell-surface receptor for the complex retinol-retinol binding protein (RBP/RBP4). Ultimately increasing cellular retinol uptake from the retinol-RBP complex, Stra6 removes retinol from RBP/RPB4 and transports it across the plasma membrane, where it is metabolized. Stra6 is broadly expressed, with 4 named isoforms that exist as a result of alternative splicing events. Mutations in the gene encoding Stra6 cause Matthew-Wood Syndrome, also known as Spear Syndrome. This syndrome is characterized by anophtalmia, mild facial dysmorphism and malformations of the heart, lung and diaphragm. The Stra6 gene maps to chromosome 15q24.1.

ID gène: 64220

UniProt: Q9BX79

Pathways: Feeding Behaviour