GBE1 Antikörper (AA 79-515) (Cy3)

Produktnummer ABIN7993390

Der Kaninchen Polyklonal anti-GBE1 Antikörper wird verwendet zum Nachweis von GBE1 in Proben von Human, Maus und Ratte. Er wurde validiert für FACS.

Kurzübersicht für GBE1 Antikörper (AA 79-515) (Cy3) (ABIN7993390)

Target: GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GBE1 Antikörper ist konjugiert mit Cy3

Applikation: Flow Cytometry (FACS)

Produktdetails anti-GBE1 Antikörper (Cy3)

Bindungsspezifität: AA 79-515

Verwendungszweck: Anti-GBE1 Antibody Cy3 Conjugated

Homologie: Human GBE1 shares 92.4% amino acid (aa) sequence identity with mouse GBE1.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human GBE1 recombinant protein (Position: H79-R515). Human GBE1 shares 92.4% amino acid (aa) sequence identity with mouse GBE1.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, 1-3 μg/1x10⁶ cells

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 GBE1

Target: GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

Andere Bezeichnung: GBE1

Hintergrund:

Background: 1,4-alpha-glucan-branching enzyme, also known as brancher enzyme or glycogen-branching enzyme is an enzyme that in humans is encoded by the GBE1 gene. The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease).

Gene Full Name: 1,4-alpha-glucan branching enzyme 1

Gen-ID: 2632

UniProt: Q04446

Pathways: Cellular Glucan Metabolic Process