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cas12157-sup-0001-FigS1.tifimage/tif4292KFig. S1. Paraffin embedded normal kidney tissue was subjected to in situ hybridization using LRP1B probe (A). Sense probe was used as control (B).
cas12157-sup-0002-FigS2.tifimage/tif3844KFig. S2. Depletion of LRP1B showed no effects on anchorage-dependent growth.
cas12157-sup-0003-FigS3.tifimage/tif2745KFig. S3. LRP1B silencing enhanced the cell proliferation on soft agar.
cas12157-sup-0004-FigS4.tifimage/tif588KFig. S4. LRP1B silencing enhanced the anchorage-independent proliferation of HEK293 cells.
cas12157-sup-0005-FigS5.tifimage/tif771KFig. S5. HEK293 cells expressing LRP1B shRNA or control vector were subjected to immunostaining with FITC-conjugated phalloidine.
cas12157-sup-0006-TableS1.docWord document36K Table S1. Sequences of oligonucleotides usded in real-time PCR, DNA bisulfite sequencing and RNAi.
cas12157-sup-0007-TableS2.docWord document208KTable S2. Summary of ISH and clinical pathologic features in 64 cases of RCC.

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