SLC27A3 Antikörper (AA 192-683) (PE)

Produktnummer ABIN7990056

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch SLC27A3 in FACS. Es zeigt Reaktivität gegenüber Proben von Human und Maus.

Kurzübersicht für SLC27A3 Antikörper (AA 192-683) (PE) (ABIN7990056)

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC27A3 Antikörper ist konjugiert mit PE

Applikation: Flow Cytometry (FACS)

Produktdetails anti-SLC27A3 Antikörper (PE)

Bindungsspezifität: AA 192-683

Verwendungszweck: Anti-FATP3/SLC27A3 Antibody PE Conjugated

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

Aufreinigung: Immunogen affinity purified.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, Optimal dilutions should be determined by end users.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Haltbarkeit: 12 months

Details zu SLC27A3

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

Andere Bezeichnung: SLC27A3

Hintergrund:

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

Gen-ID: 11000

UniProt: Q5K4L6