cation Search Results


antitrpm4 antibody  (Alomone Labs)
93
Alomone Labs antitrpm4 antibody
Antitrpm4 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
antitrpm4 antibody - by Bioz Stars, 2026-04
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dmt1  (Proteintech)
96
Proteintech dmt1
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Dmt1, supplied by Proteintech, 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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Average 96 stars, based on 1 article reviews
dmt1 - by Bioz Stars, 2026-04
96/100 stars
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bio rad 50w x8 resin  (Bio-Rad)
96
Bio-Rad bio rad 50w x8 resin
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Bio Rad 50w X8 Resin, supplied by Bio-Rad, 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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Average 96 stars, based on 1 article reviews
bio rad 50w x8 resin - by Bioz Stars, 2026-04
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cation exchange column chromatography  (Bio-Rad)
94
Bio-Rad cation exchange column chromatography
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Cation Exchange Column Chromatography, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
cation exchange column chromatography - by Bioz Stars, 2026-04
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cation exchange ag 50w x12 resin  (Bio-Rad)
95
Bio-Rad cation exchange ag 50w x12 resin
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Cation Exchange Ag 50w X12 Resin, supplied by Bio-Rad, 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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Average 95 stars, based on 1 article reviews
cation exchange ag 50w x12 resin - by Bioz Stars, 2026-04
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cation exchanger ag 50w x4  (Bio-Rad)
93
Bio-Rad cation exchanger ag 50w x4
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Cation Exchanger Ag 50w X4, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
cation exchanger ag 50w x4 - by Bioz Stars, 2026-04
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antibody against asic 3  (Novus Biologicals)
93
Novus Biologicals antibody against asic 3
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Antibody Against Asic 3, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antibody against asic 3/product/Novus Biologicals
Average 93 stars, based on 1 article reviews
antibody against asic 3 - by Bioz Stars, 2026-04
93/100 stars
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50w x2 resin  (Bio-Rad)
93
Bio-Rad 50w x2 resin
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
50w X2 Resin, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/50w x2 resin/product/Bio-Rad
Average 93 stars, based on 1 article reviews
50w x2 resin - by Bioz Stars, 2026-04
93/100 stars
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polygram ionex 25 sa na cation exchange tlc plates  (MACHEREY NAGEL)
85
MACHEREY NAGEL polygram ionex 25 sa na cation exchange tlc plates
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Polygram Ionex 25 Sa Na Cation Exchange Tlc Plates, supplied by MACHEREY NAGEL, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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benzyldimethyltetradecylammonium d7 chloride  (Toronto Research Chemicals)
88
Toronto Research Chemicals benzyldimethyltetradecylammonium d7 chloride
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Benzyldimethyltetradecylammonium D7 Chloride, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 88 stars, based on 1 article reviews
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anti trpv1  (Alomone Labs)
96
Alomone Labs anti trpv1
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Anti Trpv1, supplied by Alomone Labs, 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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cation exchange materials bio rex  (Bio-Rad)
94
Bio-Rad cation exchange materials bio rex
ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, <t>DMT1,</t> xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.
Cation Exchange Materials Bio Rex, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, DMT1, xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.

Journal: OncoTargets and Therapy

Article Title: Aloperine Induces Ferroptosis of Colorectal Cancer Cells via the Nrf2 Pathway

doi: 10.2147/OTT.S575500

Figure Lengend Snippet: ALO induces ferroptosis in CRC cells by inhibiting the Nrf2 pathway The binding conformation between ALO and the Nrf2 receptor was analyzed using AutoDock Tools. The lowest binding energy conformation was identified at the ALA-510 binding site, which interacts via a hydrogen bond with a length of 1.9 ( A ). Potential active pockets of ALO in the Nrf2 protein were evaluated using CavityPlus software; the GLY364-ALA670 domain was identified as the active binding pocket of Nrf2, and ALO bound to this pocket as expected ( B ). After treating HCT116 and SW480 cells with ALO (0 µM, 200 µM and 300 µM) for 24 hours, immunofluorescence was used to detect intracellular Nrf2 changes in HCT116 ( C and D ) and SW480 ( E and F ) cells treated with different concentrations of ALO. Western Blotting was used to detect the protein expression levels of Nrf2, DMT1, xCT and GPX4 ( G – J ). The data were expressed as mean ± SD (n = 3). * p < 0.05, compared with the control group (0 µM); # p < 0.05, compared with the 200 µM treatment group.

Article Snippet: DMT1 , 60-70 , 1:1000 , Rabbit , 20507-1-AP , Proteintech.

Techniques: Binding Assay, Software, Immunofluorescence, Western Blot, Expressing, Control