ATL1 Antikörper (AA 24-552) (PE)

Produktnummer ABIN7970719

Der Kaninchen Polyklonal anti-ATL1 Antikörper wird verwendet zum Nachweis von ATL1 in Proben von Human. Er wurde validiert für FACS.

Kurzübersicht für ATL1 Antikörper (AA 24-552) (PE) (ABIN7970719)

Target: ATL1 (Atlastin GTPase 1 (ATL1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ATL1 Antikörper ist konjugiert mit PE

Applikation: Flow Cytometry (FACS)

Produktdetails anti-ATL1 Antikörper (PE)

Bindungsspezifität: AA 24-552

Verwendungszweck: Anti-ATL1 Antibody PE Conjugated

Homologie: Human ATL1 shares 97.5%,98.3% amino acid (aa) sequence identity with mouse,rat ATL1,respectively.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human ATL1 recombinant protein (Position: E24-Q552). Human ATL1 shares 97.5% and 98.3% amino acid (aa) sequence identity with mouse and rat ATL1, respectively.

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 ATL1

Target: ATL1 (Atlastin GTPase 1 (ATL1))

Andere Bezeichnung: ATL1

Hintergrund:

Background: Atlastin, or Atlastin-1, is a protein that in humans is encoded by the ATL1 gene. The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene.

Gene Full Name: atlastin GTPase 1

Gen-ID: 51062

UniProt: Q8WXF7