Figure 5.
Western blot for A1AT in liver lysates. (A) Liver lysates prepared from Lman1cgt/cgt, Lman1gt1/gt1, Lman1−/−, and Lman1+/+ mice were analyzed by western blotting using an anti-A1AT antibody. The lower A1AT band corresponds to ER-retained A1AT (and was previously shown to be endoglycosidase H sensitive28). The upper A1AT band corresponds to post-ER A1AT and is comparable in molecular weight to secreted plasma A1AT. Each lane corresponds to an individual mouse. (B) The ratio of post-ER A1AT:ER-retained A1AT (upper band:lower band) in the hepatic lysates of each mouse as determined by densitometry; a ratio >1 indicates that the majority of the A1AT has been secreted beyond the ER, whereas a ratio <1 indicates that the majority of the A1AT is retained in the ER. Horizontal lines indicate the mean, and error bars indicate the standard error of the mean for each genotype.

Western blot for A1AT in liver lysates. (A) Liver lysates prepared from Lman1cgt/cgt, Lman1gt1/gt1, Lman1−/−, and Lman1+/+ mice were analyzed by western blotting using an anti-A1AT antibody. The lower A1AT band corresponds to ER-retained A1AT (and was previously shown to be endoglycosidase H sensitive28 ). The upper A1AT band corresponds to post-ER A1AT and is comparable in molecular weight to secreted plasma A1AT. Each lane corresponds to an individual mouse. (B) The ratio of post-ER A1AT:ER-retained A1AT (upper band:lower band) in the hepatic lysates of each mouse as determined by densitometry; a ratio >1 indicates that the majority of the A1AT has been secreted beyond the ER, whereas a ratio <1 indicates that the majority of the A1AT is retained in the ER. Horizontal lines indicate the mean, and error bars indicate the standard error of the mean for each genotype.

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