end-labeling reactions Search Results


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  • 97
    Millipore dig dutp end labeling reaction
    Dig Dutp End Labeling Reaction, supplied by Millipore, used in various techniques. Bioz Stars score: 97/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher end labeling reactions
    End Labeling Reactions, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 85/100, based on 25 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    80
    Boehringer Mannheim end labeling reaction mixture
    End Labeling Reaction Mixture, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 80/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    Roche end labeling tunel reaction
    End Labeling Tunel Reaction, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche end labelling tunel reaction
    End Labelling Tunel Reaction, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Roche dutp nick end labeling tunel reaction
    Dutp Nick End Labeling Tunel Reaction, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Roche deoxynucleotidyl transferase mediated dutp nick end labeling reaction mixture
    Deoxynucleotidyl Transferase Mediated Dutp Nick End Labeling Reaction Mixture, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche deoxynucleotidyl transferase dutp nick end labeling tunel reaction reagent
    Chronic ethanol consumption increases hepatic terminal <t>deoxynucleotidyl</t> transferase <t>dUTP</t> nick-end labeling <t>(TUNEL)</t> staining. TUNEL-positive nuclei were visualized in formalin-fixed liver sections for control- ( A ) and ethanol-fed rats ( B ). Images are representative of at least 6 rats/treatment group taken at ×40 magnification. C : for quantification, the number of TUNEL-positive cells per liver sample was counted from 20 random high-powered fields (×40 magnification). Data are expressed as the mean ± SE for 6 pairs of control- and ethanol-fed rats. * P
    Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Reaction Reagent, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche transferase dutp nick end labeling tunel reaction mixture
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Transferase Dutp Nick End Labeling Tunel Reaction Mixture, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    98
    Millipore deoxynucleotidyl transferase mediated dutp nick end labeling tunel reaction mixture
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Deoxynucleotidyl Transferase Mediated Dutp Nick End Labeling Tunel Reaction Mixture, supplied by Millipore, used in various techniques. Bioz Stars score: 98/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    89
    Roche terminal deoxynucleotidyl transferase dutp nick end labeling tunel reaction mixture
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Terminal Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Reaction Mixture, supplied by Roche, used in various techniques. Bioz Stars score: 89/100, based on 89 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Roche deoxynucleotidyl transferase dutp nick end labeling tunel reaction mix
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Reaction Mix, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche deoxynucleotidyl transferase mediated dutp nick end labeling reaction
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Deoxynucleotidyl Transferase Mediated Dutp Nick End Labeling Reaction, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche deoxynucleotidyltransferase mediated dutp biotin nick end labeling tunel reaction mixture
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Deoxynucleotidyltransferase Mediated Dutp Biotin Nick End Labeling Tunel Reaction Mixture, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche tdt mediated dutp x nick end labeling tunel reaction mixture
    Terminal transferase <t>dUTP</t> nick end labeling <t>(TUNEL)</t> assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.
    Tdt Mediated Dutp X Nick End Labeling Tunel Reaction Mixture, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Promega terminal deoxynucleotidyl transferase dutp nick end labeling tunel reaction mixture
    Apoptosis in the transplanted liver tissues (magnification, ×200). (A and B) Terminal <t>deoxynucleotidyl</t> transferase <t>dUTP</t> nick end labeling staining positive cells appear green and represent apoptotic cells, and DAPI-labeled nuclei appear blue. Apoptotic cells were scattered in the transplanted liver on POD 0 and POD 1, with no significant differences between the three groups. The numbers of apoptotic cells in the HO-1/BM-MSCs-treated group were significantly lower than those in the normal saline (NS)-treated group on POD 5, POD 7, POD 10 and POD 14. * P
    Terminal Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Reaction Mixture, supplied by Promega, used in various techniques. Bioz Stars score: 91/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche terminal deoxynucleotidyl transferase mediated nick end labeling tunel reaction
    Apoptosis in the transplanted liver tissues (magnification, ×200). (A and B) Terminal <t>deoxynucleotidyl</t> transferase <t>dUTP</t> nick end labeling staining positive cells appear green and represent apoptotic cells, and DAPI-labeled nuclei appear blue. Apoptotic cells were scattered in the transplanted liver on POD 0 and POD 1, with no significant differences between the three groups. The numbers of apoptotic cells in the HO-1/BM-MSCs-treated group were significantly lower than those in the normal saline (NS)-treated group on POD 5, POD 7, POD 10 and POD 14. * P
    Terminal Deoxynucleotidyl Transferase Mediated Nick End Labeling Tunel Reaction, supplied by Roche, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche terminal deoxynucleotidyl transferase dutp nick end labeling tunel reaction
    Apoptosis in the transplanted liver tissues (magnification, ×200). (A and B) Terminal <t>deoxynucleotidyl</t> transferase <t>dUTP</t> nick end labeling staining positive cells appear green and represent apoptotic cells, and DAPI-labeled nuclei appear blue. Apoptotic cells were scattered in the transplanted liver on POD 0 and POD 1, with no significant differences between the three groups. The numbers of apoptotic cells in the HO-1/BM-MSCs-treated group were significantly lower than those in the normal saline (NS)-treated group on POD 5, POD 7, POD 10 and POD 14. * P
    Terminal Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Reaction, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Chronic ethanol consumption increases hepatic terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining. TUNEL-positive nuclei were visualized in formalin-fixed liver sections for control- ( A ) and ethanol-fed rats ( B ). Images are representative of at least 6 rats/treatment group taken at ×40 magnification. C : for quantification, the number of TUNEL-positive cells per liver sample was counted from 20 random high-powered fields (×40 magnification). Data are expressed as the mean ± SE for 6 pairs of control- and ethanol-fed rats. * P

    Journal: American Journal of Physiology - Gastrointestinal and Liver Physiology

    Article Title: Chronic ethanol consumption enhances sensitivity to Ca2+-mediated opening of the mitochondrial permeability transition pore and increases cyclophilin D in liver

    doi: 10.1152/ajpgi.00246.2010

    Figure Lengend Snippet: Chronic ethanol consumption increases hepatic terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining. TUNEL-positive nuclei were visualized in formalin-fixed liver sections for control- ( A ) and ethanol-fed rats ( B ). Images are representative of at least 6 rats/treatment group taken at ×40 magnification. C : for quantification, the number of TUNEL-positive cells per liver sample was counted from 20 random high-powered fields (×40 magnification). Data are expressed as the mean ± SE for 6 pairs of control- and ethanol-fed rats. * P

    Article Snippet: Fifty microliters of the terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) reaction reagent (Roche, Indianapolis, IN) was added, and liver sections were incubated for 60 min in the dark at 37°C in a humidified atmosphere.

    Techniques: TUNEL Assay, Staining

    Terminal transferase dUTP nick end labeling (TUNEL) assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Induction of Thioredoxin Reductase 1 by Korean Red Ginseng Water Extract Regulates Cytoprotective Effects on Human Endothelial Cells

    doi: 10.1155/2015/972040

    Figure Lengend Snippet: Terminal transferase dUTP nick end labeling (TUNEL) assay of TrxR1 inhibition in KRG-stimulated HUVECs. KRG 1 mg/mL treated HUVECs were pretreated for 1 h with or without 2 μ M auranofin, followed 1 h by treatment with 100 μ M H 2 O 2 . After 18 h of incubation, the protective effect of KRG on H 2 O 2 -induced cell death in HUVECs and its blockage by the TrxR1 inhibitor, auranofin, were determined by the TUNEL assay DAPI, 4′,6-diamidino-2-phenylindole.

    Article Snippet: Cells were then incubated with the terminal transferase dUTP nick end labeling (TUNEL) reaction mixture (Roche, Mannheim, Germany) for 1 h at 37°C in the dark.

    Techniques: End Labeling, TUNEL Assay, Inhibition, Incubation

    Apoptosis in the transplanted liver tissues (magnification, ×200). (A and B) Terminal deoxynucleotidyl transferase dUTP nick end labeling staining positive cells appear green and represent apoptotic cells, and DAPI-labeled nuclei appear blue. Apoptotic cells were scattered in the transplanted liver on POD 0 and POD 1, with no significant differences between the three groups. The numbers of apoptotic cells in the HO-1/BM-MSCs-treated group were significantly lower than those in the normal saline (NS)-treated group on POD 5, POD 7, POD 10 and POD 14. * P

    Journal: International Journal of Molecular Medicine

    Article Title: Protective effects of heme oxygenase-1-transduced bone marrow-derived mesenchymal stem cells on reduced-size liver transplantation: Role of autophagy regulated by the ERK/mTOR signaling pathway

    doi: 10.3892/ijmm.2017.3121

    Figure Lengend Snippet: Apoptosis in the transplanted liver tissues (magnification, ×200). (A and B) Terminal deoxynucleotidyl transferase dUTP nick end labeling staining positive cells appear green and represent apoptotic cells, and DAPI-labeled nuclei appear blue. Apoptotic cells were scattered in the transplanted liver on POD 0 and POD 1, with no significant differences between the three groups. The numbers of apoptotic cells in the HO-1/BM-MSCs-treated group were significantly lower than those in the normal saline (NS)-treated group on POD 5, POD 7, POD 10 and POD 14. * P

    Article Snippet: Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) reaction mixture (Promega) was added dropwise and incubated at 37°C for 1 h. The average number of apoptotic cells was analyzed in 10 randomly selected visual fields using fluorescence microscopy (magnification, ×200; Nikon Ni-U; Nikon Corp., Tokyo, Japan), and the mean number of apoptotic cells was measured by staining cell nuclei wih DAPI (Beijing Solarbio Science & Technology Co., Ltd., Beijing, China) to determine the total number of cells.

    Techniques: TUNEL Assay, Staining, Labeling

    Fluoxetine treatment of 1 μM had no effect on cell differentiation or apoptosis of NPCs. (A) After 7 days cultured in differentiation condition, cells were collected for immunostaining detection. βIII-tubulin- and GFAP-positive cells were shown green and red, respectively. Blue DAPI staining showed the nuclei. Scale bars = 20 μm. (B) Quantitative analyses of βIII-tubulin- and GFAP-positive cells. The percentages of positive cells were shown. Values represent means ± SD (n = 6). (C) After 48h incubation, NPCs were used for TUNEL/DAPI staining. TUNEL-positive cells were green. Scale bars = 20 μm. (D) Quantitative analyses of TUNEL-positive cells. Values represent means ± SD (n = 6). DAPI, 4,6-diamidino-2-phenylindole; GFAP, anti-glial fibrillary acidic protein; NPCs, neural precursor cells; SD, standard deviation; TUNEL, transferase-mediated dUTP nick end labeling.

    Journal: International Journal of Neuropsychopharmacology

    Article Title: Fluoxetine Regulates Neurogenesis In Vitro Through Modulation of GSK-3β/β-Catenin Signaling

    doi: 10.1093/ijnp/pyu099

    Figure Lengend Snippet: Fluoxetine treatment of 1 μM had no effect on cell differentiation or apoptosis of NPCs. (A) After 7 days cultured in differentiation condition, cells were collected for immunostaining detection. βIII-tubulin- and GFAP-positive cells were shown green and red, respectively. Blue DAPI staining showed the nuclei. Scale bars = 20 μm. (B) Quantitative analyses of βIII-tubulin- and GFAP-positive cells. The percentages of positive cells were shown. Values represent means ± SD (n = 6). (C) After 48h incubation, NPCs were used for TUNEL/DAPI staining. TUNEL-positive cells were green. Scale bars = 20 μm. (D) Quantitative analyses of TUNEL-positive cells. Values represent means ± SD (n = 6). DAPI, 4,6-diamidino-2-phenylindole; GFAP, anti-glial fibrillary acidic protein; NPCs, neural precursor cells; SD, standard deviation; TUNEL, transferase-mediated dUTP nick end labeling.

    Article Snippet: After washing in PBS, the cells were permeabilized with 0.1% Triton X-100 in 0.1% sodium citrate for 2min on ice and incubated with 50 μL terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) reaction mixture (Promega) for 1h at 37°C.

    Techniques: Cell Differentiation, Cell Culture, Immunostaining, Staining, Incubation, TUNEL Assay, Standard Deviation, End Labeling