immunofluorescence staining kit Search Results


90
Beyotime immunol fluorescence staining kit
Immunol Fluorescence Staining Kit, supplied by Beyotime, 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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immunol fluorescence staining kit - by Bioz Stars, 2026-03
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baseclick GmbH 5-ethynyl-2′-deoxyuridine (edu)-click 647 kit baseclick bck-edu647
( A ) Experimental scheme indicating EdU intraperitoneal (IP) injections used to label cycling osteoblasts harvested at different time points for the data presented in panels B–D. ( B ) <t>Proliferation</t> timeline of bglap :GFP+ osteoblasts in segment –1 as determined by EdU incorporation. N (experiments)=1, n (fins)=4 (0 hpa), 10 (1 day post amputation [dpa]), 9 (2 dpa); n (rays)=14 (0, 2 dpa), 10 (1 dpa). Error bars represent 95% CI. Kruskal-Wallis test. ( C ) Proliferation of bglap :GFP+ osteoblasts in segment –2, segment –1, and segment 0 at 2 dpa. N (experiments)=1, n (fins)=9, n (rays)=14. Error bars represent 95% CI. Dunn’s test. ( D ) bglap RNAscope expression levels of EdU+ cells in segment –1 at 2 dpa. bglap -expressing osteoblasts were categorised based on RNAscope signal intensity into ‘high’ (yellow), ‘medium’ (cyan), and ‘low’ (red) using a look-up table, with ‘high’ threshold corresponding to expression levels in segment –2. N (experiments)=1, n (fins)=9, n (rays)=12, n (cells)=62. Error bars repesent SD. Scale bar, 10 µm.
5 Ethynyl 2′ Deoxyuridine (Edu) Click 647 Kit Baseclick Bck Edu647, supplied by baseclick GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/5-ethynyl-2′-deoxyuridine (edu)-click 647 kit baseclick bck-edu647/product/baseclick GmbH
Average 90 stars, based on 1 article reviews
5-ethynyl-2′-deoxyuridine (edu)-click 647 kit baseclick bck-edu647 - by Bioz Stars, 2026-03
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Porvair Sciences double-staining immunofluorescence kit the vectafluor duet kit
( A ) Experimental scheme indicating EdU intraperitoneal (IP) injections used to label cycling osteoblasts harvested at different time points for the data presented in panels B–D. ( B ) <t>Proliferation</t> timeline of bglap :GFP+ osteoblasts in segment –1 as determined by EdU incorporation. N (experiments)=1, n (fins)=4 (0 hpa), 10 (1 day post amputation [dpa]), 9 (2 dpa); n (rays)=14 (0, 2 dpa), 10 (1 dpa). Error bars represent 95% CI. Kruskal-Wallis test. ( C ) Proliferation of bglap :GFP+ osteoblasts in segment –2, segment –1, and segment 0 at 2 dpa. N (experiments)=1, n (fins)=9, n (rays)=14. Error bars represent 95% CI. Dunn’s test. ( D ) bglap RNAscope expression levels of EdU+ cells in segment –1 at 2 dpa. bglap -expressing osteoblasts were categorised based on RNAscope signal intensity into ‘high’ (yellow), ‘medium’ (cyan), and ‘low’ (red) using a look-up table, with ‘high’ threshold corresponding to expression levels in segment –2. N (experiments)=1, n (fins)=9, n (rays)=12, n (cells)=62. Error bars repesent SD. Scale bar, 10 µm.
Double Staining Immunofluorescence Kit The Vectafluor Duet Kit, supplied by Porvair Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/double-staining immunofluorescence kit the vectafluor duet kit/product/Porvair Sciences
Average 90 stars, based on 1 article reviews
double-staining immunofluorescence kit the vectafluor duet kit - by Bioz Stars, 2026-03
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Ribobio co edu immunofluorescence staining kit
( A ) Experimental scheme indicating EdU intraperitoneal (IP) injections used to label cycling osteoblasts harvested at different time points for the data presented in panels B–D. ( B ) <t>Proliferation</t> timeline of bglap :GFP+ osteoblasts in segment –1 as determined by EdU incorporation. N (experiments)=1, n (fins)=4 (0 hpa), 10 (1 day post amputation [dpa]), 9 (2 dpa); n (rays)=14 (0, 2 dpa), 10 (1 dpa). Error bars represent 95% CI. Kruskal-Wallis test. ( C ) Proliferation of bglap :GFP+ osteoblasts in segment –2, segment –1, and segment 0 at 2 dpa. N (experiments)=1, n (fins)=9, n (rays)=14. Error bars represent 95% CI. Dunn’s test. ( D ) bglap RNAscope expression levels of EdU+ cells in segment –1 at 2 dpa. bglap -expressing osteoblasts were categorised based on RNAscope signal intensity into ‘high’ (yellow), ‘medium’ (cyan), and ‘low’ (red) using a look-up table, with ‘high’ threshold corresponding to expression levels in segment –2. N (experiments)=1, n (fins)=9, n (rays)=12, n (cells)=62. Error bars repesent SD. Scale bar, 10 µm.
Edu Immunofluorescence Staining Kit, supplied by Ribobio co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/edu immunofluorescence staining kit/product/Ribobio co
Average 90 stars, based on 1 article reviews
edu immunofluorescence staining kit - by Bioz Stars, 2026-03
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Cytelligen Inc ctc immunofluorescence staining kit
( A ) Experimental scheme indicating EdU intraperitoneal (IP) injections used to label cycling osteoblasts harvested at different time points for the data presented in panels B–D. ( B ) <t>Proliferation</t> timeline of bglap :GFP+ osteoblasts in segment –1 as determined by EdU incorporation. N (experiments)=1, n (fins)=4 (0 hpa), 10 (1 day post amputation [dpa]), 9 (2 dpa); n (rays)=14 (0, 2 dpa), 10 (1 dpa). Error bars represent 95% CI. Kruskal-Wallis test. ( C ) Proliferation of bglap :GFP+ osteoblasts in segment –2, segment –1, and segment 0 at 2 dpa. N (experiments)=1, n (fins)=9, n (rays)=14. Error bars represent 95% CI. Dunn’s test. ( D ) bglap RNAscope expression levels of EdU+ cells in segment –1 at 2 dpa. bglap -expressing osteoblasts were categorised based on RNAscope signal intensity into ‘high’ (yellow), ‘medium’ (cyan), and ‘low’ (red) using a look-up table, with ‘high’ threshold corresponding to expression levels in segment –2. N (experiments)=1, n (fins)=9, n (rays)=12, n (cells)=62. Error bars repesent SD. Scale bar, 10 µm.
Ctc Immunofluorescence Staining Kit, supplied by Cytelligen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/ctc immunofluorescence staining kit/product/Cytelligen Inc
Average 90 stars, based on 1 article reviews
ctc immunofluorescence staining kit - by Bioz Stars, 2026-03
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MEDIPAN GmbH primary antibodies binding to γh2ax and 53bp1
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
Primary Antibodies Binding To γh2ax And 53bp1, supplied by MEDIPAN GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies binding to γh2ax and 53bp1/product/MEDIPAN GmbH
Average 90 stars, based on 1 article reviews
primary antibodies binding to γh2ax and 53bp1 - by Bioz Stars, 2026-03
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Quantum Dot Inc quantum dot immunofluorescent double staining reagent kit
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
Quantum Dot Immunofluorescent Double Staining Reagent Kit, supplied by Quantum Dot Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/quantum dot immunofluorescent double staining reagent kit/product/Quantum Dot Inc
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quantum dot immunofluorescent double staining reagent kit - by Bioz Stars, 2026-03
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MEDIPAN GmbH ch2ax immunofluorescence staining kit
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
Ch2ax Immunofluorescence Staining Kit, supplied by MEDIPAN GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/ch2ax immunofluorescence staining kit/product/MEDIPAN GmbH
Average 90 stars, based on 1 article reviews
ch2ax immunofluorescence staining kit - by Bioz Stars, 2026-03
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MEDIPAN GmbH immunofluorescence staining kit
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
Immunofluorescence Staining Kit, supplied by MEDIPAN GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/immunofluorescence staining kit/product/MEDIPAN GmbH
Average 90 stars, based on 1 article reviews
immunofluorescence staining kit - by Bioz Stars, 2026-03
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Becton Dickinson direct immunofluorescence staining kit
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
Direct Immunofluorescence Staining Kit, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/direct immunofluorescence staining kit/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
direct immunofluorescence staining kit - by Bioz Stars, 2026-03
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Beyotime antimouse cy3 immunofluorescence staining kit
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
Antimouse Cy3 Immunofluorescence Staining Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antimouse cy3 immunofluorescence staining kit/product/Beyotime
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antimouse cy3 immunofluorescence staining kit - by Bioz Stars, 2026-03
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Abmart Inc 4-color multiplex immunofluorescence staining kit mfihc04a
Time-dependent studies on <t>53BP1-specific</t> staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of <t>53BP1</t> focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.
4 Color Multiplex Immunofluorescence Staining Kit Mfihc04a, supplied by Abmart Inc, 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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Image Search Results


( A ) Experimental scheme indicating EdU intraperitoneal (IP) injections used to label cycling osteoblasts harvested at different time points for the data presented in panels B–D. ( B ) Proliferation timeline of bglap :GFP+ osteoblasts in segment –1 as determined by EdU incorporation. N (experiments)=1, n (fins)=4 (0 hpa), 10 (1 day post amputation [dpa]), 9 (2 dpa); n (rays)=14 (0, 2 dpa), 10 (1 dpa). Error bars represent 95% CI. Kruskal-Wallis test. ( C ) Proliferation of bglap :GFP+ osteoblasts in segment –2, segment –1, and segment 0 at 2 dpa. N (experiments)=1, n (fins)=9, n (rays)=14. Error bars represent 95% CI. Dunn’s test. ( D ) bglap RNAscope expression levels of EdU+ cells in segment –1 at 2 dpa. bglap -expressing osteoblasts were categorised based on RNAscope signal intensity into ‘high’ (yellow), ‘medium’ (cyan), and ‘low’ (red) using a look-up table, with ‘high’ threshold corresponding to expression levels in segment –2. N (experiments)=1, n (fins)=9, n (rays)=12, n (cells)=62. Error bars repesent SD. Scale bar, 10 µm.

Journal: eLife

Article Title: Zebrafish fin regeneration involves generic and regeneration-specific osteoblast injury responses

doi: 10.7554/eLife.77614

Figure Lengend Snippet: ( A ) Experimental scheme indicating EdU intraperitoneal (IP) injections used to label cycling osteoblasts harvested at different time points for the data presented in panels B–D. ( B ) Proliferation timeline of bglap :GFP+ osteoblasts in segment –1 as determined by EdU incorporation. N (experiments)=1, n (fins)=4 (0 hpa), 10 (1 day post amputation [dpa]), 9 (2 dpa); n (rays)=14 (0, 2 dpa), 10 (1 dpa). Error bars represent 95% CI. Kruskal-Wallis test. ( C ) Proliferation of bglap :GFP+ osteoblasts in segment –2, segment –1, and segment 0 at 2 dpa. N (experiments)=1, n (fins)=9, n (rays)=14. Error bars represent 95% CI. Dunn’s test. ( D ) bglap RNAscope expression levels of EdU+ cells in segment –1 at 2 dpa. bglap -expressing osteoblasts were categorised based on RNAscope signal intensity into ‘high’ (yellow), ‘medium’ (cyan), and ‘low’ (red) using a look-up table, with ‘high’ threshold corresponding to expression levels in segment –2. N (experiments)=1, n (fins)=9, n (rays)=12, n (cells)=62. Error bars repesent SD. Scale bar, 10 µm.

Article Snippet: To analyse cell proliferation, 5-ethynyl-2′-deoxyuridine (EdU)-Click 647 kit (baseclick GmbH BCK-EdU647) was used.

Techniques: RNAscope, Expressing

Time-dependent studies on 53BP1-specific staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of 53BP1 focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.

Journal: Cancers

Article Title: Heterogeneous Formation of DNA Double-Strand Breaks and Cell-Free DNA in Leukemia T-Cell Line and Human Peripheral Blood Mononuclear Cells in Response to Topoisomerase II Inhibitors

doi: 10.3390/cancers16223798

Figure Lengend Snippet: Time-dependent studies on 53BP1-specific staining in PBMCs and Jurkat cells after treatment with either ETP (25 µM) or DOX (1.0 µM): Automated quantification of cellular immunofluorescence between 0 and 8 h of incubation with topoisomerase II inhibitors using the AKLIDES ® system. DMSO-treated cells were used as a control. Percentage of 53BP1 focus-positive cells in ( A ) PBMCs and ( B ) Jurkat cells were determined at the indicated time points; quantification of 53BP1 foci number per cell in ( C ) PBMCs and ( D ) Jukat cells. Bars represent the mean and standard deviation of four independent experiments. Numbers of asterisks indicate increasing significance levels: * p ≤ 0.05. ETP: etoposide; DOX: doxorubicin.

Article Snippet: The cells were incubated with a commercially provided admixture of two primary antibodies, binding to γH2AX and 53BP1 (Medipan, Germany) in PBS with 1% BSA at the indicated dilutions for 1 h at room temperature.

Techniques: Staining, Immunofluorescence, Incubation, Control, Standard Deviation