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. 2018 Jul 23;115(32):E7642–E7649. doi: 10.1073/pnas.1721418115

Fig. 1.

Fig. 1.

Analysis of Slc30a8 RNA and protein in islets from male R138X mice on chow diet. (A) Slc30a8 RNA in situ hybridization of pancreatic islets isolated from wild-type, knockout, and R138X mice. KO islets were used as negative control. Red, glucagon RNA; green, insulin RNA; white, Slc30a8 RNA. (B) Quantification of islet Slc30a8 RNA levels using qPCR analysis. n.d., not detected. (C) Western blot of islets isolated from chow-fed WT, KO, and R138X mice. KO islets were used as negative control. The arrow indicates SLC30A8 protein; asterisks denote unspecific bands. (D) Dithizone staining of pancreatic islets isolated from WT, KO, and R138X mice.