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. 2020 Nov 16;4(22):5635–5643. doi: 10.1182/bloodadvances.2020002523

Figure 5.

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.