SLC6A17 Antikörper (AA 1-694) (HRP)

Produktnummer ABIN8040526

Der HRP-konjugierte Kaninchen Polyklonal anti-SLC6A17 Antikörper (ABIN8040526) detektiert spezifisch SLC6A17 in WB, ELISA und IHC. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.

Kurzübersicht für SLC6A17 Antikörper (AA 1-694) (HRP) (ABIN8040526)

Target: SLC6A17 (Solute Carrier Family 6, Member 17 (SLC6A17))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC6A17 Antikörper ist konjugiert mit HRP

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

Produktdetails anti-SLC6A17 Antikörper (HRP)

Bindungsspezifität: AA 1-694

Verwendungszweck: Anti-SLC6A17 Antibody HRP Conjugated

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

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human SLC6A17 recombinant protein (Position: M1-Y694).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, 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.

Lagerung: -20 °C

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

Haltbarkeit: 12 months

Details zu SLC6A17

Target: SLC6A17 (Solute Carrier Family 6, Member 17 (SLC6A17))

Andere Bezeichnung: SLC6A17

Hintergrund:

Background: The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability.

Gene Full Name: solute carrier family 6 member 17

Gen-ID: 388662

UniProt: Q9H1V8