| Autor: |
Zvi Schwartz, Barbara D. Boyan, Thomas W. Jacobs, D. Joshua Cohen, Anjali Verma |
| Rok vydání: |
2023 |
| DOI: |
10.1158/1541-7786.22513890 |
| Popis: |
Supplemental Table 1: Gene expression primers used in quantitative real-time PCR. Supplemental Table 2: Antibodies used in western blots. Figure S1: The effect of 24R,25(OH)2D3 on MDA-MB-231 cells. Figure S2: The effect of 24R,25(OH)2D3 on T-47D cells. Figure S3: Silencing CAV1 in HCC38 cells. Figure S4: Whole western blot of silencing of caveolin-1 in HCC38 cells from Supplemental Figure S3. Figure S5: Overexpression of ESR1 in HCC38 changes ERα isoform expression. Figure S6: Whole western blot of transient overexpression of ESR1 in HCC38 cells from Supplemental Figure S5. Figure S7: Overexpression of ESR1 in C2C12. Figure S8: Whole western blot of stable overexpression of ESR1 in C2C12 cells from Supplemental Figure 7. Figure S9: ERα66 was stably knocked down in MCF7 using a recombinant plasmid with a puromycin antibiotic resistant selection marker. Figure S10: Whole western blot of stable silencing of ERα66 in MCF7 cells from Supplemental Figure 9. Figure S11: Silencing the ERα66 isoform reversed the pro-apoptotic effect of 24R,25(OH)2D3 on MCF7 cells. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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