multiple dna sequence alignment feature Search Results


t 47d  (ATCC)
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ATCC t 47d
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New England Biolabs assays q5 high fidelity dna polymerase neb
Assays Q5 High Fidelity Dna Polymerase Neb, supplied by New England Biolabs, 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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Ribobio co cell-lighttmedu dna cell proliferation kit
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Thermo Fisher magmax dna multi sample ultra 2 0 kit
Magmax Dna Multi Sample Ultra 2 0 Kit, 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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zr  (ATCC)
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ATCC zr
Zr, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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New England Biolabs t4 dna ligase reaction buffer
T4 Dna Ligase Reaction Buffer, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Beyotime dna damage assay kit
a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) <t>using</t> <t>Annexin</t> V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing <t>DNA</t> double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.
Dna Damage Assay Kit, 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
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Beyotime terminal deoxynucleotidyl transferase dutp nick end labeling
a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) <t>using</t> <t>Annexin</t> V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing <t>DNA</t> double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.
Terminal Deoxynucleotidyl Transferase Dutp Nick End Labeling, 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
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TATAA Biocenter AB protein±dna interactions
a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) <t>using</t> <t>Annexin</t> V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing <t>DNA</t> double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.
Protein±Dna Interactions, supplied by TATAA Biocenter AB, 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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Becton Dickinson multiple tissue cdna (mtctm) panel ii
a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) <t>using</t> <t>Annexin</t> V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing <t>DNA</t> double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.
Multiple Tissue Cdna (Mtctm) Panel Ii, 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
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ATCC cancer cell lines du 145
a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) <t>using</t> <t>Annexin</t> V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing <t>DNA</t> double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.
Cancer Cell Lines Du 145, supplied by ATCC, 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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Vazyme Biotech Co overlapping pcr
a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) <t>using</t> <t>Annexin</t> V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing <t>DNA</t> double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.
Overlapping Pcr, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) using Annexin V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing DNA double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: Efficient active hydrogen delivery for drug-free radiation enteritis therapy in mice

doi: 10.1038/s41467-025-64270-9

Figure Lengend Snippet: a Schematic illustration of the radioprotective mechanism of H x MoO 3 @SA@COS nanomachines. b Cell viability of HIEC-6, MODEK and RAW264.7 cells treated with different concentrations of H x MoO 3 @SA@COSs. c Radioprotective effects of H x MoO 3 @SA@COSs on HIEC-6 cells at various radiation doses, with significance compared to controls. d − i Representative fluorescence images showing the uptake profile of H x MoO 3 @SA@COSs ( d ) and intracellular ROS levels ( e ) in HIEC-6 cells under different treatments, flow cytometry analysis ( f ) using Annexin V-FITC/PI staining was performed to assess apoptosis and necrosis, with corresponding quantitative results for mean fluorescence intensity (MFI) of FITC ( g ) and DCFH-DA ( h ), along with cell apoptosis percentages ( i ). Experiments were independently repeated three times ( d ) or five times ( e ) with similar results. j , l Immunofluorescence images of γ-H2AX showing DNA double-strand breaks ( j ), with corresponding quantification ( l ). k − n Macrophage polarization, visualized via CD86 (M1) and CD206 (M2) expression ( k ), with quantitative results ( m, n ). n = 3 ( b − n ) or n = 5 ( h , l ) biologically independent replicates, data are presented as mean ± SD (one way ANOVA and Tukey′s multiple comparisons tests). Source data are provided as a Source Data file.

Article Snippet: Total Antioxidant Capacity Assay Kit with ABTS method, Total Superoxide Dismutase Assay Kit with WST-8, Lipid Peroxidation MDA Assay Kit, Reactive Oxygen Species Assay Kit, Annexin V-FITC Apoptosis Detection Kit, DNA Damage Assay Kit by γ-H2AX Immunofluorescence, Cell Counting Kit-8, and Hoechst 33342 were acquired from Beyotime Biotechnology (Shanghai, China).

Techniques: Fluorescence, Flow Cytometry, Staining, Immunofluorescence, Expressing