rabbit polyclonal anti atp2c1  (Thermo Fisher)

Journal: iScience

Article Title: Genome-wide CRISPR-Cas9 screens identify mechanisms of BET bromodomain inhibitor sensitivity

doi: 10.1016/j.isci.2021.103323

Figure Lengend Snippet: Validation of whole-genome JQ1 sensitivity screen (A) Growth of HCT116- WT , HCT116- ATP2C1 , HCT116- DUSP5 , and HCT116- FERMT2 in the presence of control medium or medium supplemented with JQ1 using the IncuCyte ZOOM live cell imaging system over 132 h. Cell growth is displayed as phase object confluence (percent) analyzed with the IncuCyte ZOOM Basic Analyzer. (B) Dose response of JQ1 on cell proliferation of HCT116- WT and HCT116- ATP2C1 cells. Cell number is measured using the CellTiter-Glo luminescence assay. Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3). (C) Dose response of Paclitaxel on cell proliferation of HCT116- WT , HCT116- ATP2C1 , HCT116- DUSP5 , and HCT116- FERMT2 cells. Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3)

Article Snippet: Rabbit polyclonal anti-ATP2C1 , Invitrogen , Cat#PA5-109430.

Techniques: Live Cell Imaging, Luminescence Assay

Journal: iScience

Article Title: Genome-wide CRISPR-Cas9 screens identify mechanisms of BET bromodomain inhibitor sensitivity

doi: 10.1016/j.isci.2021.103323

Figure Lengend Snippet: Manganese modulates cellular sensitivity to JQ1 (A) Genome wide CRISPR-Cas9 screen profiles highlighting ATP2C1 and TMEM165, in HCT116 -WT cells. The left panel shows the relative abundance of ATP2C1 and TMEM165 sgRNAs compared with the initial library. The next two panels show the relative abundance of ATP2C1 and TMEM165 sgRNAs upon JQ1 treatment at IC 20 (0.2 μM) (middle panel) and IC 50 (1 μM) (right panel) compared with untreated cells. (B) Dose response effects of JQ1, JQ1 (−), or OTX015 on cell proliferation of HCT116- WT cells in the presence of different concentrations of CaCl 2 . Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3). (C) Dose response of JQ1, JQ1 (−), or OTX015 on cell proliferation of HCT116- WT cells in the presence of different concentrations of MnCl 2 . Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3). (D) Dose response of JQ1 on cell proliferation of HT-29 cells in the presence of different concentrations of MnCl 2 . Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3). (E) Dose response of JQ1 on cell proliferation of SUM159PT cells in the presence of different concentrations of MnCl 2 . Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3). (F) Dose response of JQ1, JQ1 (−), and OTX015 on cell proliferation of HCT116- ATP2C1 cells in the presence of different concentrations of MnCl 2 . (Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3). (G) Dose response of JQ1, JQ1 (−), and OTX015 on cell proliferation of HCT116- ATP2C1 cells in the presence of different concentrations of CaCl 2 . (Luminescence values are normalized to 100% in control medium to enable comparison between different cell lines. Mean ± S.D. (n = 3).

Article Snippet: Rabbit polyclonal anti-ATP2C1 , Invitrogen , Cat#PA5-109430.

Techniques: Genome Wide, CRISPR

Journal: iScience

Article Title: Genome-wide CRISPR-Cas9 screens identify mechanisms of BET bromodomain inhibitor sensitivity

doi: 10.1016/j.isci.2021.103323

Figure Lengend Snippet: BET bromodomain inhibitors increase intracellular manganese levels (A) Intracellular levels of manganese measured with the Fura-2 assay in HCT116- WT cells grown in either control medium or with an additional 50 μM MnCl 2 . Dose response effects of JQ1, JQ1 (−), the inactive enantiomer of JQ1, OTX015, I-BET762, and I-BET151. Values are normalized to control medium without compound (two-way ANOVA with Dunnett's multiple comparisons test). Mean ± S.D., n = 8. ∗ p = 0.0151, ∗∗ p = 0.0058, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (B) Intracellular levels of manganese measured with the Fura-2 assay in Caco-2 cells grown in either control medium or with an additional 50 μM MnCl 2 . Dose response effects of JQ1 or I-BET151. Values are normalized to control medium without compound (two-way ANOVA with Dunnett's multiple comparisons test) Mean ± S.D., n = 8, ∗p = 0.0208, ∗∗p = 0.0056, ∗∗∗∗p < 0.0001. (C) Intracellular levels of manganese measured with the Fura-2 assay in HCT116- WT compared with HCT116- ATP2C1 cells in 50 μM MnCl 2 . Dose response effects of JQ1. Values are normalized to HCT116- WT in control medium without compound (two-way ANOVA with Dunnett's multiple comparisons test). Mean ± S.D., n = 8. #### p < 0.0001, ∗ p = 0.0136, ∗∗∗∗ p < 0.0001. (D) Metal ion analysis using ICP-MS (Inductively Coupled Plasma Mass Spectrometry) was performed on pellets of HCT116- WT cells after overnight exposure to either DMSO, 1 μM JQ1, or 1 μM JQ1 (−), the inactive enantiomer (two-way ANOVA with Dunnett's multiple comparisons test). Mean ± S.D., n = 3. ∗∗∗∗ p < 0.0001.

Article Snippet: Rabbit polyclonal anti-ATP2C1 , Invitrogen , Cat#PA5-109430.

Techniques: Mass Spectrometry

Journal: iScience

Article Title: Genome-wide CRISPR-Cas9 screens identify mechanisms of BET bromodomain inhibitor sensitivity

doi: 10.1016/j.isci.2021.103323

Figure Lengend Snippet:

Article Snippet: Rabbit polyclonal anti-ATP2C1 , Invitrogen , Cat#PA5-109430.

Techniques: Recombinant, Synthesized, Cell Viability Assay, dsDNA Assay, Bicinchoninic Acid Protein Assay, CRISPR, Sequencing, Software