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Fig. 2 | Hereditas

Fig. 2

From: A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype

Fig. 2

a By using SDS-PAGE to characterize the purified fibrinogens (3 μg), there were three bands compatible with the Aα, Bβ, and γ chains in the healthy donor and patients. b By using western blotting with anti-FGG polyclonal antibody, the single band position in the patients was consistent with that of the γ-chain from the healthy donor

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Hereditas

ISSN: 1601-5223

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