anti nf h Search Results


98
AvesLabs anti neurofilament
Anti Neurofilament, supplied by AvesLabs, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Proteintech antibodies against nf 200
Antibodies Against Nf 200, supplied by Proteintech, 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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93
Santa Cruz Biotechnology nfh
ATX-101 inhibits stemness phenotype and induces a reversion of Neural/proneural to mesenchymal phenotype. ( A ) Confocal analyses of Ki67- and Sox2-stained GSCs-5 cells treated with ATX-101 (1.0 and 2.5 μM) for 48 h. Bar indicates 25 μm. ( B ) FACS analyses for mesenchymal markers CD44 and CD90 in GSCs-5 cells after treatment with ATX-101 (1.0, 2.5, and 5 μM) for 48 h. Percentages of cells positive for CD44, CD90, GAP43, and βIII tubulin after treatment with ATX-101 are summarized in the table below the histograms. ( C ) ICC analyses performed on GSCs-5 cells for CD44, Stro1, <t>NFH,</t> OCT3/4, <t>and</t> <t>GFAP</t> after treatment with ATX-101 (1.0, 2.5, and 5 μM) for 48 h. Bar indicates 10 μm.
Nfh, supplied by Santa Cruz Biotechnology, 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/product/anti+nf+h/NF-H+Antibody/pmc08773508-48-21-29
Average 93 stars, based on 1 article reviews
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93
Novus Biologicals rabbit anti mouse neurofilament heavy chain nf h antibody
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Rabbit Anti Mouse Neurofilament Heavy Chain Nf H Antibody, supplied by Novus Biologicals, 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/product/anti+nf+h/NF-H+Antibody/pmc12717242-93-8-15
Average 93 stars, based on 1 article reviews
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94
Novus Biologicals mouse monoclonal anti nfh conjugated to alexafluor 488
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Mouse Monoclonal Anti Nfh Conjugated To Alexafluor 488, supplied by Novus Biologicals, 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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Novus Biologicals rt 97
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Rt 97, supplied by Novus Biologicals, 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+nf+h/NF-H+Antibody+(RT97)/pm37996528-557-11-13
Average 94 stars, based on 1 article reviews
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94
Novus Biologicals antibodies against neurofilament heavy protein nf h
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Antibodies Against Neurofilament Heavy Protein Nf H, supplied by Novus Biologicals, 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+nf+h/NF-H+Antibody/pm37462535-244-13-23
Average 94 stars, based on 1 article reviews
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94
Novus Biologicals mouse anti nf
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Mouse Anti Nf, supplied by Novus Biologicals, 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+nf+h/NF-H+Antibody+(RT97)/bio_rxiv__64898__2026__03__22__713398-101-76-78
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94
Novus Biologicals rabbit anti neurofilament h
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Rabbit Anti Neurofilament H, supplied by Novus Biologicals, 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+nf+h/NF-H+Antibody/pmc04312875-107-22-26
Average 94 stars, based on 1 article reviews
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90
Biorbyt mouse neuro lament nf h antibody
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Mouse Neuro Lament Nf H Antibody, supplied by Biorbyt, 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/product/anti+nf+h/NF-H+antibody/ppr0129676-206-23-29
Average 90 stars, based on 1 article reviews
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93
Novus Biologicals anti nfh chicken polyclonal
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Anti Nfh Chicken Polyclonal, supplied by Novus Biologicals, 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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93
Novus Biologicals neurofilament heavy chain nf h primary antibody
Fluorescence staining of myelin and <t>neurofilament</t> heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain <t>(NF-H)</t> for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)
Neurofilament Heavy Chain Nf H Primary Antibody, supplied by Novus Biologicals, 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/product/anti+nf+h/NF-H+Antibody+(RNF402)/pm34445504-137-42-48
Average 93 stars, based on 1 article reviews
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Image Search Results


ATX-101 inhibits stemness phenotype and induces a reversion of Neural/proneural to mesenchymal phenotype. ( A ) Confocal analyses of Ki67- and Sox2-stained GSCs-5 cells treated with ATX-101 (1.0 and 2.5 μM) for 48 h. Bar indicates 25 μm. ( B ) FACS analyses for mesenchymal markers CD44 and CD90 in GSCs-5 cells after treatment with ATX-101 (1.0, 2.5, and 5 μM) for 48 h. Percentages of cells positive for CD44, CD90, GAP43, and βIII tubulin after treatment with ATX-101 are summarized in the table below the histograms. ( C ) ICC analyses performed on GSCs-5 cells for CD44, Stro1, NFH, OCT3/4, and GFAP after treatment with ATX-101 (1.0, 2.5, and 5 μM) for 48 h. Bar indicates 10 μm.

Journal: Cancers

Article Title: ATX-101, a Peptide Targeting PCNA, Has Antitumor Efficacy Alone or in Combination with Radiotherapy in Murine Models of Human Glioblastoma

doi: 10.3390/cancers14020289

Figure Lengend Snippet: ATX-101 inhibits stemness phenotype and induces a reversion of Neural/proneural to mesenchymal phenotype. ( A ) Confocal analyses of Ki67- and Sox2-stained GSCs-5 cells treated with ATX-101 (1.0 and 2.5 μM) for 48 h. Bar indicates 25 μm. ( B ) FACS analyses for mesenchymal markers CD44 and CD90 in GSCs-5 cells after treatment with ATX-101 (1.0, 2.5, and 5 μM) for 48 h. Percentages of cells positive for CD44, CD90, GAP43, and βIII tubulin after treatment with ATX-101 are summarized in the table below the histograms. ( C ) ICC analyses performed on GSCs-5 cells for CD44, Stro1, NFH, OCT3/4, and GFAP after treatment with ATX-101 (1.0, 2.5, and 5 μM) for 48 h. Bar indicates 10 μm.

Article Snippet: Antibodies against β-actin (sc-69879), PCNA (sc-56), p-Histone H2AX (Ser 139) (γH2A, sc-517348), DNA-PKcs (sc-390849), GFAP (sc-3673), Oct-3/4 (sc-5279), β3 Tubulin (sc-80005), NFH (sc-133237), and Sox2 (sc-365823) were purchased from Santa Cruz (Santa Cruz, CA, USA).

Techniques: Staining

Fluorescence staining of myelin and neurofilament heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain (NF-H) for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)

Journal: Journal of Neuroimmune Pharmacology

Article Title: Histamine H3 Receptor Antagonist, Thioperamide, Improves Behavioral and Neuropathological Changes Associated with Subclinical Hypersensitivity to a Cow’s Milk Allergen

doi: 10.1007/s11481-025-10256-9

Figure Lengend Snippet: Fluorescence staining of myelin and neurofilament heavy chain in the anterior cingulate. Brain sections from male ( a ) and female ( b ) sham and BLG mice with vehicle (Veh) and thioperamide (Thio) treatment were stained with FluoroMyelin™ (FM) and neurofilament heavy chain (NF-H) for myelin sheath (red) and axonal structure (green), respectively. DAPI nuclear counterstain was used to identify cell bodies (blue). Representative photomicrographs were taken from the anterior cingulate region of the frontal cortex using a 10× objective. Scale bar = 200 μm. Staining differences among the experimental groups were compared by randomly selecting three samples from each group and quantifying the optical density (OD) of FM staining ( c ) and NF-H immunostaining ( d ) within the anterior cingulate cortex. The bars indicate the relative OD value for each treatment group ± SEM ( n = 3). Sex-disaggregated analyses were performed by 2-way ANOVA, and asterisks between two bars indicate significance (** p < 0.01, *** p < 0.001, **** p < 0.0001)

Article Snippet: The brain sections were subsequently incubated with a rabbit anti-mouse neurofilament heavy chain (NF-H) antibody (Novus Biologicals, Centennial, CO, USA; Catalog # NB300-135, RRID: AB_350460) at a 1:3,000 dilution overnight at 4 °C.

Techniques: Fluorescence, Staining, Immunostaining