tripan blue exclusion test Search Results


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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
Tripan Blue, supplied by Nacalai, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
Tripan Blue, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells <t>(DMSO,</t> <t>PTX-short,</t> ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) <t>Tripan</t> blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.
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The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells (DMSO, PTX-short, ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) Tripan blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.

Journal: Scientific Reports

Article Title: Eribulin induces micronuclei and enhances the nuclear localization of cGAS in triple-negative breast cancer cells

doi: 10.1038/s41598-024-64651-y

Figure Lengend Snippet: The effects of KD-cGAS on cell proliferation was evaluated. MM231 cells (DMSO, PTX-short, ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI) were used ( a ) Proliferation assay was performed. 24 h after knockdown of cGAS was defined as 0 h, and cell proliferation was evaluated every 12 h. ( b ) Tripan blue stain was used to evaluate the percentage of live and dead cells 24 h after treatment. ( c ) We evaluated the effects of knocking down of cGAS on RAD51 expression. Vinculin was used as loading control. ( d ) Immunofluorescence with RAD51 and γH2Ax was performed. DAPI was used for nuclear staining. The white line is 10 μm. ( e ) We counted the number of nuclear foci in each cell stained with γH2Ax and RAD51 on average. The meaning of the asterisks are as follows: *p < 0.05, **p < 0.01.

Article Snippet: The cell lysates from MM231 cell lines (DMSO, PTX-short, ERI-short, KD-cGAS-DMSO, KD-cGAS-PTX, KD-cGAS-ERI), which were 24 h after PTX or ERI treatment, were extracted and diluted equally by tripan blue (Nacalai, #20577-34).

Techniques: Proliferation Assay, Knockdown, Staining, Expressing, Control, Immunofluorescence