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Fig. 5 | BMC Medical Genetics

Fig. 5

From: The identification and characterization of the p.G91 deletion in CRYBA1 in a Chinese family with congenital cataracts

Fig. 5

Immunofluorescence staining of exogenous WT and mutated CRYBA1 in 2 cell lines. After the WT and deleted forms of CRYBA1 cDNA constructs were transfected into 293 T and SRA lines, cells were stained with FLAG primary antibody. p.G91del mutation led to greater aggregation of the protein at the cell membrane. Blue: nuclear; green: exogenous CRYBA1, scale bar: 20 μM

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