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Az3146

Manufactured by Merck Group
Sourced in United States

The AZ3146 is a precision laboratory instrument designed for specialized applications in scientific research and analysis. It is a highly versatile and accurate device that can perform various measurement and testing functions. The core function of the AZ3146 is to provide reliable and consistent data collection and analysis, catering to the needs of researchers and scientists across various disciplines. Further details on the intended use of this product are not available.

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4 protocols using az3146

1

HeLa Cell Line Characterization and Maintenance

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All cell lines used in this study were derived from HeLa Flp‐in cells (a gift from S Taylor, University of Manchester, UK) (Tighe et al, 2008 (link)), which were authenticated by STR profiling (Eurofins). Cells were cultured in full‐growth media—DMEM supplemented with 9% FBS and 50 μg/ml penicillin/streptomycin. While doing fluorescence time‐lapse analysis, cells were cultured in Leibovitz's L‐15 media (900 mg/L D+ galactose, 5 mM Sodium pyruvate and no phenol red) supplemented with 9% FBS and 50 μg/ml penicillin/streptomycin, or DMEM (no phenol red) supplemented with 9% FBS and 50 μg/ml penicillin/streptomycin. Every 4–8 weeks, cells were screened to ensure a mycoplasma‐free culture.
Doxycycline (1 μg/ml), STLC (S‐trityl‐L‐cysteine: 10 μM), thymidine (2 mM), nocodazole (3.3 μM), MG132 (10 μM) and the MPS1 inhibitor AZ‐3146 (2.5 μM) were purchased from Sigma Aldrich; puromycin (1 mg/ml) and hygromycin B (200 μg/ml) from Santa Cruz Biotechnology; RO‐3306 (10 μM) from Tocris; the PLK1 inhibitor BI‐2536 (100 nM) from SelleckBio; the BUB1 inhibitor BAY‐1816032 (5 μM) from MedChemExpress; the SiR‐DNA far‐red DNA probe (1:10,000) from Spirochrome.
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2

Antibody Sources and Reagents for Cell Analysis

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Antibodies were obtained from the following sources: anti-Cdc20 (14866), anti-securin (13445), anti-phospho-p53 (9284), anti-γ-H2A.X (9718), Apc2 (12301), and anti-Rad21 (4321) IgGs were from Cell Signaling Technologies; anti-β-actin (mAb C4), anti-p21 (F-5), anti-p53 (6243); anti-c-myc (mAb 9E10) IgGs were from Santa Cruz Biotechnology; anti-p16 ARC (mAb EP1551Y) was from Abcam; anti-Caspase-3 (ADI-AAP-113) IgG was from Enzo Life Sciences, Inc. Apcin, pro-TAME, and TDZD-8 were from Cayman Chemical. 5-FU, cisplatin, etoposide, AZ3146, lithium chloride, and chloroquine were from Sigma–Aldrich. Lamba protein phosphatase was from New England Biolabs. MG-132 was from EMD Millipore. Silencer Select negative control siRNA, Silencer Select Cdc20 siRNA, and Silencer Select Securin siRNAs were from Thermo Fisher Scientific. All other biochemical reagents were of the highest available purity and were commercially obtained.
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3

Microtubule-Targeting Agents and Inhibitors

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Microtubule‐targeting agents taxol, epothilone B and vincristine, Aurora inhibitor VX‐680, spindle assembly checkpoint inhibitor AZ3146, and cytokinesis inhibitor blebbistatin were from Sigma‐Aldrich (St Louis, MO, USA). Hydroxycamptothecin and mitomycin C were from Selleck Chemicals (Houston, TX, USA).
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4

Analyzing Mitotic Chromosome Segregation

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Chromosome segregation analysis was performed on MEFs stably expressing H2B-RFP, as previously described (Malureanu et al., 2009 (link)). In mitotic timing experiments, the time interval between nuclear envelope breakdown (NEBD) and anaphase onset was measured in H2B-mRFP positive cells by monitoring unchallenged mitoses. Briefly, cells undergoing NEBD were marked and monitored at two minute intervals until anaphase onset. For SAC sensitivity experiments, cells were treated with nocodazole (Sigma-Aldrich) at a final concentration of either 20 or 10 ng/ml and then monitored from NEBD to anaphase onset. nocodazole challenge experiments were performed as previously described (Malureanu et al., 2009 (link)). Briefly, nocodazole was added to a final concentration of 100 ng/ml. Cells undergoing NEBD were marked and monitored at 10 min intervals to determine when they decondensed their chromosomes. The duration of arrest in mitosis, which is defined as the interval between NEBD (onset of mitosis) and chromatin decondensation (exit from mitosis without cytokinesis), was then calculated and plotted. For checkpoint silencing and sensitivity experiments, 500 nM or 2 µM AZ3146 (Sigma-Aldrich) was added either concurrently or in sequence with nocodazole. All experiments were performed on at least three independently generated MEF lines unless stated.
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