SLC27A3 anticorps (AA 192-683) (APC)

N° du produit ABIN7990055

Cet anticorps anti-SLC27A3 Polyclonal Lapin conjugué à APC (ABIN7990055) détecte spécifiquement SLC27A3 dans FACS. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour SLC27A3 anticorps (AA 192-683) (APC) (ABIN7990055)

Antigène: SLC27A3 (FATP3) (Fatty Acid Transport Protein 3 (FATP3))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC27A3 est conjugé à/à la APC

Application: Flow Cytometry (FACS)

Détail du produit anti-SLC27A3 anticorps (APC)

Épitope: AA 192-683

Fonction: Anti-FATP3/SLC27A3 Antibody APC Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human FATP3/SLC27A3 recombinant protein (Position: L192-I683).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur SLC27A3

Antigène: SLC27A3 (FATP3) (Fatty Acid Transport Protein 3 (FATP3))

Autre désignation: SLC27A3

Sujet:

Background: Long-chain fatty acid transport protein 3 is a protein that in humans is encoded by the SLC27A3 gene. This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants.

Gene Full Name: solute carrier family 27 member 3

ID gène: 11000

UniProt: Q5K4L6