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tunel staining  (Vazyme Biotech Co)
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Vazyme Biotech Co tunel staining
YBX1 regulates angiogenesis <t>and</t> <t>apoptosis</t> in HUVECs through the HIF-1α pathway. ( A–H ) Western blot results and quantification of HIF-1α, VEGFA, Bcl-2, Bax, cleaved PARP, and cleaved Caspase-3 expression levels after overexpression of HIF-1α in the context of YBX1 knockdown. ( I ) <t>TUNEL</t> staining of control, H/R and different treatment groups evaluating by fluorescence microscope. Magnification = 40×; Scale bar = 50 µm. ( J ) Double ICC labeling for VEGFA and CD31 in HUVECs with YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 50 µm. ( K ) Scratch wound healing assay showing changes in cell migration ability among different treatment groups. Magnification = 100×; Scale bar = 500 µm. ( L ) Transwell migration assay assessing invasion capacity after YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 125 µm. * P < 0.05 versus the control group, # P < 0.05 versus the H/R group, ◆ P < 0.05 versus the H/R + siNC group, & P < 0.05 versus the H/R + siYBX1. Data are presented as mean ± SEM ( n = 6). Means were compared by 1-way ANOVA with Tukey's multiple comparison post hoc tests.
Tunel Staining, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tunel staining/product/Vazyme Biotech Co
Average 96 stars, based on 1 article reviews
tunel staining - by Bioz Stars, 2026-03
96/100 stars
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tunel staining kit  (TaKaRa)
96
TaKaRa tunel staining kit
YBX1 regulates angiogenesis <t>and</t> <t>apoptosis</t> in HUVECs through the HIF-1α pathway. ( A–H ) Western blot results and quantification of HIF-1α, VEGFA, Bcl-2, Bax, cleaved PARP, and cleaved Caspase-3 expression levels after overexpression of HIF-1α in the context of YBX1 knockdown. ( I ) <t>TUNEL</t> staining of control, H/R and different treatment groups evaluating by fluorescence microscope. Magnification = 40×; Scale bar = 50 µm. ( J ) Double ICC labeling for VEGFA and CD31 in HUVECs with YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 50 µm. ( K ) Scratch wound healing assay showing changes in cell migration ability among different treatment groups. Magnification = 100×; Scale bar = 500 µm. ( L ) Transwell migration assay assessing invasion capacity after YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 125 µm. * P < 0.05 versus the control group, # P < 0.05 versus the H/R group, ◆ P < 0.05 versus the H/R + siNC group, & P < 0.05 versus the H/R + siYBX1. Data are presented as mean ± SEM ( n = 6). Means were compared by 1-way ANOVA with Tukey's multiple comparison post hoc tests.
Tunel Staining Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tunel staining kit/product/TaKaRa
Average 96 stars, based on 1 article reviews
tunel staining kit - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier
terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining  (Vazyme Biotech Co)
96
Vazyme Biotech Co terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining
YBX1 regulates angiogenesis <t>and</t> <t>apoptosis</t> in HUVECs through the HIF-1α pathway. ( A–H ) Western blot results and quantification of HIF-1α, VEGFA, Bcl-2, Bax, cleaved PARP, and cleaved Caspase-3 expression levels after overexpression of HIF-1α in the context of YBX1 knockdown. ( I ) <t>TUNEL</t> staining of control, H/R and different treatment groups evaluating by fluorescence microscope. Magnification = 40×; Scale bar = 50 µm. ( J ) Double ICC labeling for VEGFA and CD31 in HUVECs with YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 50 µm. ( K ) Scratch wound healing assay showing changes in cell migration ability among different treatment groups. Magnification = 100×; Scale bar = 500 µm. ( L ) Transwell migration assay assessing invasion capacity after YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 125 µm. * P < 0.05 versus the control group, # P < 0.05 versus the H/R group, ◆ P < 0.05 versus the H/R + siNC group, & P < 0.05 versus the H/R + siYBX1. Data are presented as mean ± SEM ( n = 6). Means were compared by 1-way ANOVA with Tukey's multiple comparison post hoc tests.
Terminal Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Staining, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining/product/Vazyme Biotech Co
Average 96 stars, based on 1 article reviews
terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier
terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining kit  (Vazyme Biotech Co)
96
Vazyme Biotech Co terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining kit
YBX1 regulates angiogenesis <t>and</t> <t>apoptosis</t> in HUVECs through the HIF-1α pathway. ( A–H ) Western blot results and quantification of HIF-1α, VEGFA, Bcl-2, Bax, cleaved PARP, and cleaved Caspase-3 expression levels after overexpression of HIF-1α in the context of YBX1 knockdown. ( I ) <t>TUNEL</t> staining of control, H/R and different treatment groups evaluating by fluorescence microscope. Magnification = 40×; Scale bar = 50 µm. ( J ) Double ICC labeling for VEGFA and CD31 in HUVECs with YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 50 µm. ( K ) Scratch wound healing assay showing changes in cell migration ability among different treatment groups. Magnification = 100×; Scale bar = 500 µm. ( L ) Transwell migration assay assessing invasion capacity after YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 125 µm. * P < 0.05 versus the control group, # P < 0.05 versus the H/R group, ◆ P < 0.05 versus the H/R + siNC group, & P < 0.05 versus the H/R + siYBX1. Data are presented as mean ± SEM ( n = 6). Means were compared by 1-way ANOVA with Tukey's multiple comparison post hoc tests.
Terminal Deoxynucleotidyl Transferase Dutp Nick End Labeling Tunel Staining Kit, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining kit/product/Vazyme Biotech Co
Average 96 stars, based on 1 article reviews
terminal deoxynucleotidyl transferase dutp nick end labeling tunel staining kit - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier
terminal deoxynucleotidyl transferase mediated dutp nick end labeling tunel staining  (Vazyme Biotech Co)
96
Vazyme Biotech Co terminal deoxynucleotidyl transferase mediated dutp nick end labeling tunel staining
A . Representative and the corresponding local enlarged images of H&E, <t>TUNEL</t> (Green), CD11b (Red), Ly6G (Cyan), Ly6C (Magenta) staining of mice tumor from each treatment group, counterstained with DAPI (Blue). B-E . Quantification of TUNEL positive ( B ), CD11b + ( C ), Ly6G + ( D ), Ly6C + ( E ) cells in tumor tissue (n=3). F . Representative (left) and the corresponding local enlarged (right) images of H&E and CD11b (Red) staining of mice tumor from naïve and vaccine-cured mice tumor, counterstained with DAPI (Blue). G . Quantification of CD11b + cells in tumor tissue (n=3). All error bars represent means ± s.e.m. Statistical significance was determined by one-way ANOVA. * p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns means no significance.
Terminal Deoxynucleotidyl Transferase Mediated Dutp Nick End Labeling Tunel Staining, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/terminal deoxynucleotidyl transferase mediated dutp nick end labeling tunel staining/product/Vazyme Biotech Co
Average 96 stars, based on 1 article reviews
terminal deoxynucleotidyl transferase mediated dutp nick end labeling tunel staining - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier

Image Search Results


YBX1 regulates angiogenesis and apoptosis in HUVECs through the HIF-1α pathway. ( A–H ) Western blot results and quantification of HIF-1α, VEGFA, Bcl-2, Bax, cleaved PARP, and cleaved Caspase-3 expression levels after overexpression of HIF-1α in the context of YBX1 knockdown. ( I ) TUNEL staining of control, H/R and different treatment groups evaluating by fluorescence microscope. Magnification = 40×; Scale bar = 50 µm. ( J ) Double ICC labeling for VEGFA and CD31 in HUVECs with YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 50 µm. ( K ) Scratch wound healing assay showing changes in cell migration ability among different treatment groups. Magnification = 100×; Scale bar = 500 µm. ( L ) Transwell migration assay assessing invasion capacity after YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 125 µm. * P < 0.05 versus the control group, # P < 0.05 versus the H/R group, ◆ P < 0.05 versus the H/R + siNC group, & P < 0.05 versus the H/R + siYBX1. Data are presented as mean ± SEM ( n = 6). Means were compared by 1-way ANOVA with Tukey's multiple comparison post hoc tests.

Journal: Investigative Ophthalmology & Visual Science

Article Title: YBX1 Modulated Corneal Neovascularization Induced by Alkali Burn via m 5 C-Dependent Regulation of the STAT3/HIF-1α/VEGFA Axis

doi: 10.1167/iovs.67.2.42

Figure Lengend Snippet: YBX1 regulates angiogenesis and apoptosis in HUVECs through the HIF-1α pathway. ( A–H ) Western blot results and quantification of HIF-1α, VEGFA, Bcl-2, Bax, cleaved PARP, and cleaved Caspase-3 expression levels after overexpression of HIF-1α in the context of YBX1 knockdown. ( I ) TUNEL staining of control, H/R and different treatment groups evaluating by fluorescence microscope. Magnification = 40×; Scale bar = 50 µm. ( J ) Double ICC labeling for VEGFA and CD31 in HUVECs with YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 50 µm. ( K ) Scratch wound healing assay showing changes in cell migration ability among different treatment groups. Magnification = 100×; Scale bar = 500 µm. ( L ) Transwell migration assay assessing invasion capacity after YBX1 knockdown and HIF-1α overexpression. Magnification = 400×; Scale bar = 125 µm. * P < 0.05 versus the control group, # P < 0.05 versus the H/R group, ◆ P < 0.05 versus the H/R + siNC group, & P < 0.05 versus the H/R + siYBX1. Data are presented as mean ± SEM ( n = 6). Means were compared by 1-way ANOVA with Tukey's multiple comparison post hoc tests.

Article Snippet: Cell apoptosis was assessed via TUNEL staining (Vazyme, Cat #A112).

Techniques: Western Blot, Expressing, Over Expression, Knockdown, TUNEL Assay, Staining, Control, Fluorescence, Microscopy, Labeling, Wound Healing Assay, Migration, Transwell Migration Assay, Comparison

A . Representative and the corresponding local enlarged images of H&E, TUNEL (Green), CD11b (Red), Ly6G (Cyan), Ly6C (Magenta) staining of mice tumor from each treatment group, counterstained with DAPI (Blue). B-E . Quantification of TUNEL positive ( B ), CD11b + ( C ), Ly6G + ( D ), Ly6C + ( E ) cells in tumor tissue (n=3). F . Representative (left) and the corresponding local enlarged (right) images of H&E and CD11b (Red) staining of mice tumor from naïve and vaccine-cured mice tumor, counterstained with DAPI (Blue). G . Quantification of CD11b + cells in tumor tissue (n=3). All error bars represent means ± s.e.m. Statistical significance was determined by one-way ANOVA. * p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns means no significance.

Journal: bioRxiv

Article Title: In vivo vaccine generation with a topical small molecule cocktail to eradicates AML and PDAC

doi: 10.1101/2025.10.19.683274

Figure Lengend Snippet: A . Representative and the corresponding local enlarged images of H&E, TUNEL (Green), CD11b (Red), Ly6G (Cyan), Ly6C (Magenta) staining of mice tumor from each treatment group, counterstained with DAPI (Blue). B-E . Quantification of TUNEL positive ( B ), CD11b + ( C ), Ly6G + ( D ), Ly6C + ( E ) cells in tumor tissue (n=3). F . Representative (left) and the corresponding local enlarged (right) images of H&E and CD11b (Red) staining of mice tumor from naïve and vaccine-cured mice tumor, counterstained with DAPI (Blue). G . Quantification of CD11b + cells in tumor tissue (n=3). All error bars represent means ± s.e.m. Statistical significance was determined by one-way ANOVA. * p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns means no significance.

Article Snippet: The terminal Deoxynucleotidyl Transferase-Mediated dUTP Nick End Labeling (TUNEL) staining was carried out on mouse tumors using the TUNEL Bright Green Apoptosis Detection Kit (A112-03, Vazyme), according to the manufacturer’s instructions.

Techniques: TUNEL Assay, Staining