PYGM Antikörper (AA 390-804) (Fluoro647)

Produktnummer ABIN8022443

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

Kurzübersicht für PYGM Antikörper (AA 390-804) (Fluoro647) (ABIN8022443)

Target: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PYGM Antikörper ist konjugiert mit Fluoro647

Applikation: Flow Cytometry (FACS)

Produktdetails anti-PYGM Antikörper (Fluoro647)

Bindungsspezifität: AA 390-804

Verwendungszweck: Anti-PYGM Antibody Fluoro647 Conjugated

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

Homologie: Human PYGMshares 95.9%,94.2% amino acid (aa) sequence identity with mouse,rat PYGM,respectively.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human PYGM recombinant protein (Position: V390-R804). Human PYGMshares 95.9% and 94.2% amino acid (aa) sequence identity with mouse and rat PYGM, 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 PYGM

Target: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Andere Bezeichnung: PYGM

Hintergrund:

Background: This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.

Gene Full Name: glycogen phosphorylase, muscle associated

Gen-ID: 5837

UniProt: P11217

Pathways: Cellular Glucan Metabolic Process