anti elane antibody Search Results


93
Atlas Antibodies anti elane antibody
Fig. 3. Rapid thawing increased cryoablation-induced neutrophil infiltration and NETosis in vivo. (a) Representative images of NETs shown by immunofluorescence staining of Hoechst-positive DNA (blue), <t>histone</t> <t>H2B-positive</t> histone (green), and <t>ELANE-positive</t> NE (red) in the skin at 1 day after cryoablation. Scale bar = 5 μm. White arrows indicate NETs identified by the co-localization of Hoechst, histone H2B, and ELANE. (b) Representative images of immunofluorescence staining for Hoechst-positive DNA (blue), histone H2B-positive chromatin (green), and ELANE-positive neutrophils (red) in the skin at 1 day after cryoablation, with or without rapid thawing. Scale bar = 40 μm. (c) Quantification of infiltrating neutrophils and NETs in the skin at 1 day after cryoablation, with or without rapid thawing, performed by counting ELANE-positive cells for neutrophils and cells positive for Hoechst, histone H2B, and ELANE for NETs, respectively. Values were determined in 6 random microscopic fields in n = 3 per group. Values represent mean ± SEM. * *P < 0.01. One-way ANOVA followed by Tukey-Kramer test was used for c. NET, neutrophil extracellular trap; NE, neutrophil elastase; Ctl, control; Cryo, cryoablation.
Anti Elane Antibody, supplied by Atlas Antibodies, 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
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94
Boster Bio anti ne boster pb10058
Fig. 3. Rapid thawing increased cryoablation-induced neutrophil infiltration and NETosis in vivo. (a) Representative images of NETs shown by immunofluorescence staining of Hoechst-positive DNA (blue), <t>histone</t> <t>H2B-positive</t> histone (green), and <t>ELANE-positive</t> NE (red) in the skin at 1 day after cryoablation. Scale bar = 5 μm. White arrows indicate NETs identified by the co-localization of Hoechst, histone H2B, and ELANE. (b) Representative images of immunofluorescence staining for Hoechst-positive DNA (blue), histone H2B-positive chromatin (green), and ELANE-positive neutrophils (red) in the skin at 1 day after cryoablation, with or without rapid thawing. Scale bar = 40 μm. (c) Quantification of infiltrating neutrophils and NETs in the skin at 1 day after cryoablation, with or without rapid thawing, performed by counting ELANE-positive cells for neutrophils and cells positive for Hoechst, histone H2B, and ELANE for NETs, respectively. Values were determined in 6 random microscopic fields in n = 3 per group. Values represent mean ± SEM. * *P < 0.01. One-way ANOVA followed by Tukey-Kramer test was used for c. NET, neutrophil extracellular trap; NE, neutrophil elastase; Ctl, control; Cryo, cryoablation.
Anti Ne Boster Pb10058, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+elane+antibody/Anti-Neutrophil+Elastase%2FELANE+Antibody+Picoband/pm41764726-69-18-19
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94
Bioss neutrophil elastase polyclonal antibody
Fig. 3. Rapid thawing increased cryoablation-induced neutrophil infiltration and NETosis in vivo. (a) Representative images of NETs shown by immunofluorescence staining of Hoechst-positive DNA (blue), <t>histone</t> <t>H2B-positive</t> histone (green), and <t>ELANE-positive</t> NE (red) in the skin at 1 day after cryoablation. Scale bar = 5 μm. White arrows indicate NETs identified by the co-localization of Hoechst, histone H2B, and ELANE. (b) Representative images of immunofluorescence staining for Hoechst-positive DNA (blue), histone H2B-positive chromatin (green), and ELANE-positive neutrophils (red) in the skin at 1 day after cryoablation, with or without rapid thawing. Scale bar = 40 μm. (c) Quantification of infiltrating neutrophils and NETs in the skin at 1 day after cryoablation, with or without rapid thawing, performed by counting ELANE-positive cells for neutrophils and cells positive for Hoechst, histone H2B, and ELANE for NETs, respectively. Values were determined in 6 random microscopic fields in n = 3 per group. Values represent mean ± SEM. * *P < 0.01. One-way ANOVA followed by Tukey-Kramer test was used for c. NET, neutrophil extracellular trap; NE, neutrophil elastase; Ctl, control; Cryo, cryoablation.
Neutrophil Elastase Polyclonal Antibody, 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
https://www.bioz.com/product/anti+elane+antibody/Neutrophil+Elastase+Polyclonal+Antibody/custom%40bs-6982r%4027904056
Average 94 stars, based on 1 article reviews
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86
Elan Drug Technologies anti a antibody isotypes on plaque removal
Fig. 3. Rapid thawing increased cryoablation-induced neutrophil infiltration and NETosis in vivo. (a) Representative images of NETs shown by immunofluorescence staining of Hoechst-positive DNA (blue), <t>histone</t> <t>H2B-positive</t> histone (green), and <t>ELANE-positive</t> NE (red) in the skin at 1 day after cryoablation. Scale bar = 5 μm. White arrows indicate NETs identified by the co-localization of Hoechst, histone H2B, and ELANE. (b) Representative images of immunofluorescence staining for Hoechst-positive DNA (blue), histone H2B-positive chromatin (green), and ELANE-positive neutrophils (red) in the skin at 1 day after cryoablation, with or without rapid thawing. Scale bar = 40 μm. (c) Quantification of infiltrating neutrophils and NETs in the skin at 1 day after cryoablation, with or without rapid thawing, performed by counting ELANE-positive cells for neutrophils and cells positive for Hoechst, histone H2B, and ELANE for NETs, respectively. Values were determined in 6 random microscopic fields in n = 3 per group. Values represent mean ± SEM. * *P < 0.01. One-way ANOVA followed by Tukey-Kramer test was used for c. NET, neutrophil extracellular trap; NE, neutrophil elastase; Ctl, control; Cryo, cryoablation.
Anti A Antibody Isotypes On Plaque Removal, supplied by Elan Drug Technologies, 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/anti+elane+antibody/a+anti+antibody+isotypes+on+plaque+removal/10__1016_slash_s0197___4580_ascii40_02_ascii41_00052___0-5554-4-35
Average 86 stars, based on 1 article reviews
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Rabbit anti-Human ELANE Polyclonal Antibody
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N/A
This antibody is specificfor neutrophil elastase as demonstrated by immunoelectrophoresis and ELISA.Elastasesform a subfamily of serine proteases that hydrolyze many proteins in additionto elastin. Humans have six elastase genes which encode the structurallysimilar proteins. The
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Boster Bio Anti-Neutrophil elastase ELANE Antibody catalog # A01607. Tested in WB,IHC,ICC/IF applications. This antibody reacts with Human,Mouse,Rat.
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N/A
Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode structurally similar proteins. The encoded preproprotein is proteolytically processed to generate the active
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Image Search Results


Fig. 3. Rapid thawing increased cryoablation-induced neutrophil infiltration and NETosis in vivo. (a) Representative images of NETs shown by immunofluorescence staining of Hoechst-positive DNA (blue), histone H2B-positive histone (green), and ELANE-positive NE (red) in the skin at 1 day after cryoablation. Scale bar = 5 μm. White arrows indicate NETs identified by the co-localization of Hoechst, histone H2B, and ELANE. (b) Representative images of immunofluorescence staining for Hoechst-positive DNA (blue), histone H2B-positive chromatin (green), and ELANE-positive neutrophils (red) in the skin at 1 day after cryoablation, with or without rapid thawing. Scale bar = 40 μm. (c) Quantification of infiltrating neutrophils and NETs in the skin at 1 day after cryoablation, with or without rapid thawing, performed by counting ELANE-positive cells for neutrophils and cells positive for Hoechst, histone H2B, and ELANE for NETs, respectively. Values were determined in 6 random microscopic fields in n = 3 per group. Values represent mean ± SEM. * *P < 0.01. One-way ANOVA followed by Tukey-Kramer test was used for c. NET, neutrophil extracellular trap; NE, neutrophil elastase; Ctl, control; Cryo, cryoablation.

Journal: Journal of dermatological science

Article Title: Rapid thawing enhances tissue destruction in a mouse model of cutaneous cryoablation: Insights into oxidative stress and neutrophil activation.

doi: 10.1016/j.jdermsci.2025.02.003

Figure Lengend Snippet: Fig. 3. Rapid thawing increased cryoablation-induced neutrophil infiltration and NETosis in vivo. (a) Representative images of NETs shown by immunofluorescence staining of Hoechst-positive DNA (blue), histone H2B-positive histone (green), and ELANE-positive NE (red) in the skin at 1 day after cryoablation. Scale bar = 5 μm. White arrows indicate NETs identified by the co-localization of Hoechst, histone H2B, and ELANE. (b) Representative images of immunofluorescence staining for Hoechst-positive DNA (blue), histone H2B-positive chromatin (green), and ELANE-positive neutrophils (red) in the skin at 1 day after cryoablation, with or without rapid thawing. Scale bar = 40 μm. (c) Quantification of infiltrating neutrophils and NETs in the skin at 1 day after cryoablation, with or without rapid thawing, performed by counting ELANE-positive cells for neutrophils and cells positive for Hoechst, histone H2B, and ELANE for NETs, respectively. Values were determined in 6 random microscopic fields in n = 3 per group. Values represent mean ± SEM. * *P < 0.01. One-way ANOVA followed by Tukey-Kramer test was used for c. NET, neutrophil extracellular trap; NE, neutrophil elastase; Ctl, control; Cryo, cryoablation.

Article Snippet: The antibodies used and their sources were as follows: anti-CD3 antibody (ab5690; Abcam), anti-CD8 antibody (Abcam), anti-ELANE antibody (HPA066836; Atlas antibodies), and anti-Histone H2B antibody (ab134211; Abcam).

Techniques: In Vivo, Immunofluorescence, Staining, Control