4 hydroxynonenal polyclonal antibody Search Results


96
Bioss ferritin
Ferritin, supplied by Bioss, 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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Bioss alexa fluor 647
Alexa Fluor 647, supplied by Bioss, 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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Bioss alexa fluor 488
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92
Bioss unconjugated rabbit polyclonal antibodies
Unconjugated Rabbit Polyclonal Antibodies, supplied by Bioss, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Bioss anti 4 hydroxynonenal 4 hne polyclonal antibody
Characterization and antioxidant activity of samples. ( A ) Three types of sponges: vacuum-heated (150 °C, 16 h) gelatin sponges containing β-tricalcium phosphate (β-TCP) granules (vh-GSβ), vacuum-heated chemically synthesized gelatin sponges containing β-TCP (vhc-GSβ), and vacuum-heated chemically synthesized gelatin sponges containing EGCG and β-TCP (vhEc-GSβ). Macroscopic appearances ( left ; scale bar = 5 mm) and field-emission scanning electron microscopic appearances ( middle ; scale bar = 500 µm, right ; scale bar = 200 µm). ( B ) Quantitative analysis of pore size based on the average of the maximum Feret diameter. n = 6; one-way ANOVA with Tukey’s multiple comparisons test; ns: not significant; * p < 0.05. ( C ) X-ray powder diffraction patterns. Arrow heads: the characteristic diffraction peaks of β-TCP. ( D ) ATR-FTIR spectra of the samples. Arrows: the characteristic peaks of amide bands. ( E ) DPPH assay. ( F ) Quantitative analysis of DPPH scavenging activity using Welch’s ANOVA followed by Dunnett’s T3 multiple comparisons test. n = 4, ns: not significant, **** p < 0.0001. ( G ) Immunofluorescence staining <t>for</t> <t>4-Hydroxynonenal</t> <t>(4-HNE)</t> in rat calvarial bone defects implanted with or without samples. Scale bars: top = 50 µm; bottom = 500 µm. ( H ) Quantitative analysis of the ratio of 4-HNE to 4′,6-diamidino-2-phenylindole (DAPI) fluorescence area. n = 4; Welch’s ANOVA followed by Dunnett’s T3 multiple comparisons test; ns: not significant; ** p < 0.01.
Anti 4 Hydroxynonenal 4 Hne Polyclonal Antibody, supplied by Bioss, 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/anti 4 hydroxynonenal 4 hne polyclonal antibody/product/Bioss
Average 93 stars, based on 1 article reviews
anti 4 hydroxynonenal 4 hne polyclonal antibody - by Bioz Stars, 2026-04
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90
Bioss rabbit anti 4 hne polyclonal antibodies conjugated
Antioxidant effects of EGCG in bone defects. ( A ) Immunohistochemical staining of defects with <t>anti-4-hydroxynonenal</t> (4-HNE) antibodies (red). ( B ) Fluorescently stained area of 4-HNE. ( A ) Purple: merge of 4-HNE and DAPI image. ** p < 0.01 ( n = 3, ANOVA with Tukey-Kramer tests).
Rabbit Anti 4 Hne Polyclonal Antibodies Conjugated, supplied by Bioss, 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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93
Bioss anti 4 hydroxynonenal antibody
Antioxidant effects of EGCG in bone defects. ( A ) Immunohistochemical staining of defects with <t>anti-4-hydroxynonenal</t> (4-HNE) antibodies (red). ( B ) Fluorescently stained area of 4-HNE. ( A ) Purple: merge of 4-HNE and DAPI image. ** p < 0.01 ( n = 3, ANOVA with Tukey-Kramer tests).
Anti 4 Hydroxynonenal Antibody, supplied by Bioss, 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/anti 4 hydroxynonenal antibody/product/Bioss
Average 93 stars, based on 1 article reviews
anti 4 hydroxynonenal antibody - by Bioz Stars, 2026-04
93/100 stars
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cy3  (Bioss)
90
Bioss cy3
Antioxidant effects of EGCG in bone defects. ( A ) Immunohistochemical staining of defects with <t>anti-4-hydroxynonenal</t> (4-HNE) antibodies (red). ( B ) Fluorescently stained area of 4-HNE. ( A ) Purple: merge of 4-HNE and DAPI image. ** p < 0.01 ( n = 3, ANOVA with Tukey-Kramer tests).
Cy3, supplied by Bioss, 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
Merck KGaA rabbit polyclonal antibody against 4-hydroxynonenal (4-hne)
Antioxidant effects of EGCG in bone defects. ( A ) Immunohistochemical staining of defects with <t>anti-4-hydroxynonenal</t> (4-HNE) antibodies (red). ( B ) Fluorescently stained area of 4-HNE. ( A ) Purple: merge of 4-HNE and DAPI image. ** p < 0.01 ( n = 3, ANOVA with Tukey-Kramer tests).
Rabbit Polyclonal Antibody Against 4 Hydroxynonenal (4 Hne), supplied by Merck KGaA, 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/rabbit polyclonal antibody against 4-hydroxynonenal (4-hne)/product/Merck KGaA
Average 90 stars, based on 1 article reviews
rabbit polyclonal antibody against 4-hydroxynonenal (4-hne) - by Bioz Stars, 2026-04
90/100 stars
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N/A
Aldehydic products of lipid peroxidation, such as 4 hydroxynonenal (4 HNE), have been implicated in the etiology of pathological changes under oxidative stress as a key mediator of oxidative stress induced cell death. It is
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N/A
Aldehydic products of lipid peroxidation, such as 4 hydroxynonenal (4 HNE), have been implicated in the etiology of pathological changes under oxidative stress as a key mediator of oxidative stress induced cell death. It is
  Buy from Supplier

N/A
Aldehydic products of lipid peroxidation, such as 4 hydroxynonenal (4 HNE), have been implicated in the etiology of pathological changes under oxidative stress as a key mediator of oxidative stress induced cell death. It is
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Image Search Results


Characterization and antioxidant activity of samples. ( A ) Three types of sponges: vacuum-heated (150 °C, 16 h) gelatin sponges containing β-tricalcium phosphate (β-TCP) granules (vh-GSβ), vacuum-heated chemically synthesized gelatin sponges containing β-TCP (vhc-GSβ), and vacuum-heated chemically synthesized gelatin sponges containing EGCG and β-TCP (vhEc-GSβ). Macroscopic appearances ( left ; scale bar = 5 mm) and field-emission scanning electron microscopic appearances ( middle ; scale bar = 500 µm, right ; scale bar = 200 µm). ( B ) Quantitative analysis of pore size based on the average of the maximum Feret diameter. n = 6; one-way ANOVA with Tukey’s multiple comparisons test; ns: not significant; * p < 0.05. ( C ) X-ray powder diffraction patterns. Arrow heads: the characteristic diffraction peaks of β-TCP. ( D ) ATR-FTIR spectra of the samples. Arrows: the characteristic peaks of amide bands. ( E ) DPPH assay. ( F ) Quantitative analysis of DPPH scavenging activity using Welch’s ANOVA followed by Dunnett’s T3 multiple comparisons test. n = 4, ns: not significant, **** p < 0.0001. ( G ) Immunofluorescence staining for 4-Hydroxynonenal (4-HNE) in rat calvarial bone defects implanted with or without samples. Scale bars: top = 50 µm; bottom = 500 µm. ( H ) Quantitative analysis of the ratio of 4-HNE to 4′,6-diamidino-2-phenylindole (DAPI) fluorescence area. n = 4; Welch’s ANOVA followed by Dunnett’s T3 multiple comparisons test; ns: not significant; ** p < 0.01.

Journal: Journal of Functional Biomaterials

Article Title: Physicochemical and Antioxidant Alterations of Modified and Free Epigallocatechin Gallate Under Thermal Treatment in Air and Vacuum

doi: 10.3390/jfb17010018

Figure Lengend Snippet: Characterization and antioxidant activity of samples. ( A ) Three types of sponges: vacuum-heated (150 °C, 16 h) gelatin sponges containing β-tricalcium phosphate (β-TCP) granules (vh-GSβ), vacuum-heated chemically synthesized gelatin sponges containing β-TCP (vhc-GSβ), and vacuum-heated chemically synthesized gelatin sponges containing EGCG and β-TCP (vhEc-GSβ). Macroscopic appearances ( left ; scale bar = 5 mm) and field-emission scanning electron microscopic appearances ( middle ; scale bar = 500 µm, right ; scale bar = 200 µm). ( B ) Quantitative analysis of pore size based on the average of the maximum Feret diameter. n = 6; one-way ANOVA with Tukey’s multiple comparisons test; ns: not significant; * p < 0.05. ( C ) X-ray powder diffraction patterns. Arrow heads: the characteristic diffraction peaks of β-TCP. ( D ) ATR-FTIR spectra of the samples. Arrows: the characteristic peaks of amide bands. ( E ) DPPH assay. ( F ) Quantitative analysis of DPPH scavenging activity using Welch’s ANOVA followed by Dunnett’s T3 multiple comparisons test. n = 4, ns: not significant, **** p < 0.0001. ( G ) Immunofluorescence staining for 4-Hydroxynonenal (4-HNE) in rat calvarial bone defects implanted with or without samples. Scale bars: top = 50 µm; bottom = 500 µm. ( H ) Quantitative analysis of the ratio of 4-HNE to 4′,6-diamidino-2-phenylindole (DAPI) fluorescence area. n = 4; Welch’s ANOVA followed by Dunnett’s T3 multiple comparisons test; ns: not significant; ** p < 0.01.

Article Snippet: Frozen sections of animal tissues were blocked and permeabilized in phosphate-buffered saline (164-28713; FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan) containing 5% goat serum (S-1000, Vector Laboratories, Inc., Newark, CA, USA) and 0.3% Triton X-100 (Code 12967-32, Nacalai, Kyoto, Japan) for 30 min. Immunostaining was performed using an anti-4-hydroxynonenal (4-HNE) polyclonal antibody (bs-6313R-Cy5, Bioss Antibodies, Woburn, MA, USA; 1:100) in the dark at 4 °C overnight.

Techniques: Antioxidant Activity Assay, Synthesized, Pore Size, DPPH Assay, Activity Assay, Immunofluorescence, Staining, Fluorescence

Antioxidant effects of EGCG in bone defects. ( A ) Immunohistochemical staining of defects with anti-4-hydroxynonenal (4-HNE) antibodies (red). ( B ) Fluorescently stained area of 4-HNE. ( A ) Purple: merge of 4-HNE and DAPI image. ** p < 0.01 ( n = 3, ANOVA with Tukey-Kramer tests).

Journal: International Journal of Molecular Sciences

Article Title: Integration of Epigallocatechin Gallate in Gelatin Sponges Attenuates Matrix Metalloproteinase-Dependent Degradation and Increases Bone Formation

doi: 10.3390/ijms20236042

Figure Lengend Snippet: Antioxidant effects of EGCG in bone defects. ( A ) Immunohistochemical staining of defects with anti-4-hydroxynonenal (4-HNE) antibodies (red). ( B ) Fluorescently stained area of 4-HNE. ( A ) Purple: merge of 4-HNE and DAPI image. ** p < 0.01 ( n = 3, ANOVA with Tukey-Kramer tests).

Article Snippet: Rabbit anti-4-HNE polyclonal antibodies conjugated with Alexa Fluor 647 (cat. No. bs-6313r-a647; Bioss Inc., MA, USA; 1:200) were used to detect oxidation in the defects.

Techniques: Immunohistochemical staining, Staining