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Fibrinogen gamma chain(FGG) Contains 2 sets of 3 non-identical chains (alpha, beta and gamma),A long coiled coil structure connects the central nodule to the C-terminal domains . The long C-terminal ends of the alpha chains fold back to contributing a fourth strand to the coiled coil structure.Defects in FGG are a cause of congenital afibrinogenemia (CAFBN) . CAFBN is a rare autosomal recessive disorder,it is characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen.Patients with congenital fibrinogen abnormalities can manifest different clinical pictures,including tendency toward bleeding, clinically silent and predisposition for thrombosis with or without bleeding.
Purity: Greater than 90.0% as determined by: Endotoxin:Less than 0.1ng/μg (1EU/μg) of Fibrinogen gamma chain/FGG (Human)
·Formulation ·Reconstitution ·Storage
Please avoid freeze-thaw cycles. |