POMGNT1 Antikörper (AA 96-394) (Fluoro488)

Produktnummer ABIN8027757

Der Kaninchen Polyklonal anti-POMGNT1 Antikörper wird verwendet zum Nachweis von POMGNT1 in Proben von Human, Maus und Ratte. Er wurde validiert für FACS.

Kurzübersicht für POMGNT1 Antikörper (AA 96-394) (Fluoro488) (ABIN8027757)

Target: POMGNT1 (Protein O-Linked Mannose Beta1,2-N-Acetylglucosaminyltransferase (POMGNT1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser POMGNT1 Antikörper ist konjugiert mit Fluoro488

Applikation: Flow Cytometry (FACS)

Produktdetails anti-POMGNT1 Antikörper (Fluoro488)

Bindungsspezifität: AA 96-394

Verwendungszweck: Anti-POMGNT1 Antibody Fluoro488 Conjugated

Homologie: Human POMGNT1 shares 99.7% amino acid (aa) sequence identity with both mouse,rat POMGNT1.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human POMGNT1 recombinant protein (Position: R96-E394). Human POMGNT1 shares 99.7% amino acid (aa) sequence identity with both mouse and rat POMGNT1.

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 POMGNT1

Target: POMGNT1 (Protein O-Linked Mannose Beta1,2-N-Acetylglucosaminyltransferase (POMGNT1))

Andere Bezeichnung: POMGNT1

Hintergrund:

Background: Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 is an enzyme that in humans is encoded by the POMGNT1 gene. This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.

Gene Full Name: protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)

Gen-ID: 55624

UniProt: Q8WZA1