SLC27A3 anticorps (AA 192-683)

N° du produit ABIN7600438

L’anticorps anti-SLC27A3 Polyclonal Lapin est utilisé pour la détection de SLC27A3 dans des échantillons de Humain et Souris. Il a été validé pour WB, ELISA et IHC.

Aperçu rapide pour SLC27A3 anticorps (AA 192-683) (ABIN7600438)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC27A3 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Détail du produit anti-SLC27A3 anticorps

Épitope: AA 192-683

Fonction: Anti-FATP3/SLC27A3 Antibody

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

Attributs du produit: Anti-FATP3/SLC27A3 Antibody. Tested in ELISA, IHC, WB applications. This antibody reacts with Human, Mouse.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human, Mouse Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

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

Poids moléculaire: 70-79 kDa

ID gène: 11000

UniProt: Q5K4L6