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2 protocols using bsm 33218 m

1

Quantification of Signaling Pathway Proteins

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MSCs or ECs were lysed using ice-cold lysis buffer containing 1% protease inhibitors and phosphatase inhibitors (Roche Applied Science, Penzberg, Germany). Proteins were fractionated by sodium dodecyl sulfate (SDS)–polyacrylamide gel electrophoresis and then transferred to polyvinylidene difluoride (PVDF) membranes. Protein expression was detected by incubation with antibodies against CXCR4 (D1S7W; Cell Signaling Technology), phospho-VEGFR2 (bs-2674R; Bioss), integrin αvβ3 (bs-1310R; Bioss), p-FAK (bsm-52155R; Bioss), FAK (bs-20735R; Bioss), p-JAK2 (SY24-03; Novus), JAK2 (bs-23003R; Bioss), p-STAT3 (bs-1658R; Bioss), STAT3 (bsm-33218 M; Bioss), ATF3 (bs-0519R; Bioss), CHOP (bs-20669R; Bioss), p-ERK1/2 (D13.14.4E; Cell Signaling Technology), ERK1/2 (137F5; Cell Signaling Technology) or β-actin (AF0003; Beyotime).
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2

Western Blot Analysis of Cell Signaling

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Western blot analysis was performed as described previously. The antibodies used were as follows: rabbit anti-human DCP2 (1:1000; ab28658; abcam, Ltd), rabbit anti-human STAT3 (1:500; bsm-33218M; Bioss, Ltd), rabbit antihuman p-STAT3 (1:800; AP0248), mouse anti-human BIRC3 (1:500; MB0129), rabbit anti-human Bax (1:500; BS6420), Bcl2 (1:500; BS70205), rabbit anti-human Caspase 3 (1:1000; BS61583), rabbit anti-human Caspase 8(1:1000; AP0258), rabbit anti-human Caspase 9 (1:1000; AP0359), and rabbit anti-human GAPDH (1:3000; MB001) all from Bioworld Technology, Ltd).
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