FGG Antikörper (AA 420-449)

Produktnummer ABIN7874931

Der Kaninchen Polyklonal anti-FGG Antikörper wird verwendet zum Nachweis von FGG in Proben von Human. Er wurde validiert für WB, IF und IHC (p).

Kurzübersicht für FGG Antikörper (AA 420-449) (ABIN7874931)

Target: FGG (Fibrinogen gamma Chain (FGG))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FGG Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Produktdetails anti-FGG Antikörper

Bindungsspezifität: AA 420-449

Verwendungszweck: FGG Antibody / Fibrinogen gamma chain / FIBG

Aufreinigung: Purified

Immunogen: A portion of amino acids 420-449 from the human protein was used as the immunogen for the FGG antibody.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: The stated application concentrations are suggested starting points. Titration of the FGG antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % 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: Aliquot the FGG antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Details zu FGG

Target: FGG (Fibrinogen gamma Chain (FGG))

Andere Bezeichnung: FGG

Hintergrund: FIBG is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in its gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia.

UniProt: P02679