secondary conjugated antibodies containing dapi Search Results


96
Vector Laboratories 1x pbs
1x Pbs, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories vectashield mounting medium with dapi
Vectashield Mounting Medium With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Solarbio Inc anti-fade solution (containing dapi
Anti Fade Solution (Containing Dapi, supplied by Solarbio 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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96
SouthernBiotech secondary alexa fluor
Secondary Alexa Fluor, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
Beyotime dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
Dapi, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secondary+conjugated+antibodies+containing+dapi/DAPI/pm28779993-48-4-13
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90
FUJIFILM 1 μg/ml dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
1 μg/Ml Dapi, supplied by FUJIFILM, 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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Average 90 stars, based on 1 article reviews
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90
Carl Roth GmbH nuclear label dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
Nuclear Label Dapi, supplied by Carl Roth 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/product/secondary+conjugated+antibodies+containing+dapi/4++6+diamidino+2+phenylindole++dapi+/pm34646120-90-14-18
Average 90 stars, based on 1 article reviews
nuclear label dapi - by Bioz Stars, 2026-09
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99
Thermo Fisher 4 6 diamidino 2 phenylindole
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
4 6 Diamidino 2 Phenylindole, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
Thermo Fisher 4 6 diamidino 2 phenylindole dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
4 6 Diamidino 2 Phenylindole Dapi, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secondary+conjugated+antibodies+containing+dapi/4'%2C6'-Diamidino-2-phenylindole+dihydrochloride%2C+98%25/pmc08638109-64-54-48
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86
Nacalai dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
Dapi, supplied by Nacalai, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secondary+conjugated+antibodies+containing+dapi/dapi/bio_rxiv__64898__2025__12__22__695864-80-28-29
Average 86 stars, based on 1 article reviews
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99
Thermo Fisher pbs dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
Pbs Dapi, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/secondary+conjugated+antibodies+containing+dapi/PBS/pm39662461-62-22-24
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95
Tocris antibody with dapi
Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained <t>with</t> <t>antibodies</t> against LC3 (red color) and <t>DAPI</t> (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.
Antibody With Dapi, supplied by Tocris, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained with antibodies against LC3 (red color) and DAPI (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.

Journal: Journal of pharmacological sciences

Article Title: The Class I PI3K inhibitor S14161 induces autophagy in malignant blood cells by modulating the Beclin 1/Vps34 complex.

doi: 10.1016/j.jphs.2017.07.001

Figure Lengend Snippet: Fig. 2. S14161 induces LC3-II expression in myeloma and leukemia cells. AeB, S14161 induced LC3-II expression in a concentration-dependent manner. RPMI-8226 cells were treated with S14161 (0, 10, 20 mM) or Idelalisib (0, 100, 200 mM), or Wortmannin (0, 1, 2 mM) for 24 h, LC3 expression were detected by Western blot. C, S14161 induced LC3-II expression in various cancer cells. MM cells (OPM2, RPMI-8226, KMS11) and leukemia cells (K562) were treated with 20 mM S14161 or DMSO for 10 h. After incubation, cells were processed for analysis of LC3 and GAPDH by Western blot. D, S14161 induced LC3-II expression in a time-dependent manner. KMS11 and K562 cells were treated with 10 mM S14161 at 0, 12, 24 or 36 h, and then LC3 was detected by Western blot. E, S14161 induced LC3-II expression analyzed by a confocal microscope. K562 and OPM2 cells were starved or treated with S14161 (20 mM) alone or combination with 3-MA (0.2 mM) or BafA1 (20 nM) for 10 h. Then, cells were fixed and stained with antibodies against LC3 (red color) and DAPI (blue color) before being applied to analyze on a confocal microscope. Autophagosome formation was defined by the accumulation of LC3, arrows indicate autophagosomes. The expression ratio of LC3II over GAPDH was analyzed by densitometry.

Article Snippet: Horseradish peroxidase-conjugate secondary antibodies, DAPI (40,6-diamidino-2-phenylindole), Cy3-labeled goat anti-rabbit IgG were purchased from Beyotime Institute of Biotechnology (Nantong, China).

Techniques: Expressing, Concentration Assay, Western Blot, Incubation, Microscopy, Staining