Protocol to measure inter-centrosome distance in adherent cells using epifluorescence microscopy
We present here a protocol to assay the centrosome separation events at late-G2 phase of the cell cycle by immunofluorescence microscopy. We describe the steps required for imaging and measurement of inter-centrosome distance. Here, we use GAS2L1 as an example, but the protocol can be used to test a...
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Veröffentlicht in: | STAR protocols 2022-03, Vol.3 (1), p.101227-101227, Article 101227 |
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Zusammenfassung: | We present here a protocol to assay the centrosome separation events at late-G2 phase of the cell cycle by immunofluorescence microscopy. We describe the steps required for imaging and measurement of inter-centrosome distance. Here, we use GAS2L1 as an example, but the protocol can be used to test any protein for a role in centrosome separation and cohesion. The steps below are specific for hTERT RPE-1 cell lines, but other adherent cell lines (e.g., U2OS, MRC-5) are also amenable for this protocol.
For complete details on the use and execution of this protocol, please refer to Au et al. (2017) and Au et al. (2020).
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•Protocol to measure inter-centrosome distance in adherent cells•Approach to analyze protein involvement in centrosome separation at late G2 phase•Applicable to the analysis of centrosome cohesion and separation
We present here a protocol to assay the centrosome separation events at late-G2 phase of the cell cycle by immunofluorescence microscopy. We describe the steps required for imaging and measurement of inter-centrosome distance. Here, we use GAS2L1 as an example, but the protocol can be used to test any protein for a role in centrosome separation and cohesion. The steps below are specific for hTERT RPE-1 cell lines, but other adherent cell lines (e.g., U2OS, MRC-5) are also amenable for this protocol. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2022.101227 |