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. 2012 Sep 4;2:255–259. doi: 10.1016/j.fob.2012.08.005

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© 2012 Published by Elsevier B.V. on behalf of Federation of European Biochemical Societies.

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non- commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig. 1 — Tespa1 protein exists in the microsomal fraction in lymphocytes. (A) Western blot analysis and immunoprecipitations by using anti-Tespa1 antibody for Tespa1 protein expression in the 12 kinds of adult mouse tissues. ERK is used as a loading control. WAT, white adipose tissue. (B) Western blot analysis for Tespa1 protein expression in CD19⁺, CD4⁺, CD8⁺, and CD11b⁺ cells isolated from the adult mouse spleen. Actin is used as a loading control. (C) Western blot analysis of Tespa1, IP₃R1, IP₃R3, ATP synthase (ATP syn), and actin expressions in the subcellular fractions from the adult mouse thymus. S3, soluble cytoplasmic fraction; P2, crude mitochondrial fraction; P3, crude microsomal fraction; total, total lysate; IP, immunoprecipitations.