GLYCTK Antikörper (AA 251-350) (AbBy Fluor® 750)

Produktnummer ABIN5004268

Der Kaninchen Polyklonal Anti-GLYCTK-Antikörper wurde für WB, IF (cc) und IF (p) validiert. Er ist geeignet, GLYCTK in Proben von Maus zu detektieren.

Kurzübersicht für GLYCTK Antikörper (AA 251-350) (AbBy Fluor® 750) (ABIN5004268)

Target: GLYCTK (Glycerate Kinase (GLYCTK))

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GLYCTK Antikörper ist konjugiert mit AbBy Fluor® 750

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-GLYCTK Antikörper (AbBy Fluor® 750)

Bindungsspezifität: AA 251-350

Kreuzreaktivität: Maus

Homologie: Human,Rat

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HBEBP2/GLYCTK

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu GLYCTK

Target: GLYCTK (Glycerate Kinase (GLYCTK))

Andere Bezeichnung: HBEBP2/GLYCTK

Hintergrund:

Synonyms: CG9886 like, GLCTK_HUMAN, Glycerate kinase, Glyctk, GLYCTK1, HBeAg binding protein 2, HBeAg binding protein 4, HBeAg-binding protein 4, HBeAgBP4A, HBEBP2, HBEBP4.

Background: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.

Gen-ID: 132158