Fukutin Antikörper (Middle Region)

Produktnummer ABIN952403

Der Kaninchen Polyklonal Anti-Fukutin-Antikörper wurde für WB, IHC (p) und EIA validiert. Er ist geeignet, Fukutin in Proben von Human und Maus zu detektieren.

Kurzübersicht für Fukutin Antikörper (Middle Region) (ABIN952403)

Target: Fukutin (FKTN)

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Fukutin Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Produktdetails anti-Fukutin Antikörper

Bindungsspezifität: AA 184-214, Middle Region

Spezifität: This antibody recognizes Human and Mouse FKTN (Center).

Aufreinigung: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 184-214 amino acids from the Central region of Human Fukutin. Genename: FKTN

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu Fukutin

Target: Fukutin (FKTN)

Andere Bezeichnung: Fukutin

Hintergrund: The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.Synonyms: FCMD, FKTN, Fukuyama-type congenital muscular dystrophy protein

Molekulargewicht: 53724 Da

Gen-ID: 2218

NCBI Accession: NP_001073270

Pathways: Regulation of Carbohydrate Metabolic Process