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δnp63 flag

Manufactured by Merck Group

ΔNp63-Flag is a protein that functions as a transcription factor. It is used in research applications to study gene expression and cellular processes.

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2 protocols using δnp63 flag

1

Shp2 Regulates ΔNp63 Stability

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HEK293 cells (ATCC® CRL-1573™) cultured in six-well plates with DMEM medium containing 10% fetal bovine serum were co-transfected with a various amounts of CMV-Shp2WT (Addgene, #8381) and ΔNp63-Flag (Addgene, #26979) at 70% confluence as indicated in Fig.5A using calcium phosphate transfection kit (Thermal-Fisher Cat: K278001) according to the manufactural protocol. 48hrs post-transfection, total protein isolated from cell lysates was subjected to western blotting to detect the expression of Shp2 and ΔNp63. To test whether Shp2 regulates ΔNp63 protein stability, HEK293 cells seeded in six-well plates were co-transfected with 1µg/well CMV-Shp2WT and 2µg/well ΔNp63-Flag and treated with a different amount of MG132 (Sigma-Aldrich, Cat:1211877–36-9) as indicated in Fig.5B. 48hrs after transfection, protein level of Shp2 and ΔNp63 was examined by western blotting analysis.
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2

Shp2 Regulates ΔNp63 Stability

Check if the same lab product or an alternative is used in the 5 most similar protocols
HEK293 cells (ATCC® CRL-1573™) cultured in six-well plates with DMEM medium containing 10% fetal bovine serum were co-transfected with a various amounts of CMV-Shp2WT (Addgene, #8381) and ΔNp63-Flag (Addgene, #26979) at 70% confluence as indicated in Fig.5A using calcium phosphate transfection kit (Thermal-Fisher Cat: K278001) according to the manufactural protocol. 48hrs post-transfection, total protein isolated from cell lysates was subjected to western blotting to detect the expression of Shp2 and ΔNp63. To test whether Shp2 regulates ΔNp63 protein stability, HEK293 cells seeded in six-well plates were co-transfected with 1µg/well CMV-Shp2WT and 2µg/well ΔNp63-Flag and treated with a different amount of MG132 (Sigma-Aldrich, Cat:1211877–36-9) as indicated in Fig.5B. 48hrs after transfection, protein level of Shp2 and ΔNp63 was examined by western blotting analysis.
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