treatment rat renal fibroblast cell line nrk 49f Search Results


96
ATCC normal rat kidney nrk fibroblast cell

Normal Rat Kidney Nrk Fibroblast Cell, supplied by ATCC, 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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DSMZ rat renal interstitial fibroblasts

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Anhui Medical University rat kidney fibroblasts nrk-49f

Rat Kidney Fibroblasts Nrk 49f, supplied by Anhui Medical University, 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
Bio-Rad anti a6

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BioResource International Inc normal rat kidney interstitial fibroblast cells nrk-49f
Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal <t>interstitial</t> <t>fibroblast</t> <t>NRK-49F.</t> NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.
Normal Rat Kidney Interstitial Fibroblast Cells Nrk 49f, supplied by BioResource International Inc, 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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cells  (ATCC)
93
ATCC cells
Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal <t>interstitial</t> <t>fibroblast</t> <t>NRK-49F.</t> NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.
Cells, supplied by ATCC, 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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ATCC cell culturing normal rat kidney fibroblasts
Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal <t>interstitial</t> <t>fibroblast</t> <t>NRK-49F.</t> NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.
Cell Culturing Normal Rat Kidney Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
LGC Standards nrk 49f normal rat kidney fibroblasts
Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal <t>interstitial</t> <t>fibroblast</t> <t>NRK-49F.</t> NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.
Nrk 49f Normal Rat Kidney Fibroblasts, supplied by LGC Standards, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
China Center for Type Culture Collection normal rat kidney interstitial fibroblast line (nrk-49f)
Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal <t>interstitial</t> <t>fibroblast</t> <t>NRK-49F.</t> NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.
Normal Rat Kidney Interstitial Fibroblast Line (Nrk 49f), supplied by China Center for Type Culture Collection, 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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86
LGC Standards normal rat kidney fibroblast nrk 49f cells
A , C‐terminal of fibronectin (FBN‐C) turnover marker secretion by HK‐2 proximal tubular epithelial cells on HG and RAASi treatment. B , type IV collagen formation biomarker (PRO‐C4) secretion by HK‐2 cells on HG and RAASi treatment. C and D , PRO‐C4 secretion by <t>NRK‐49F</t> cells treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF; D ). Values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05 vs . control; §§ P < 0.01 vs . HG.
Normal Rat Kidney Fibroblast Nrk 49f Cells, supplied by LGC Standards, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
LGC Promochem nrk-49f normal rat kidney fibroblasts
A , C‐terminal of fibronectin (FBN‐C) turnover marker secretion by HK‐2 proximal tubular epithelial cells on HG and RAASi treatment. B , type IV collagen formation biomarker (PRO‐C4) secretion by HK‐2 cells on HG and RAASi treatment. C and D , PRO‐C4 secretion by <t>NRK‐49F</t> cells treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF; D ). Values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05 vs . control; §§ P < 0.01 vs . HG.
Nrk 49f Normal Rat Kidney Fibroblasts, supplied by LGC Promochem, 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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JCRB Cell Bank nrk-49f rat renal fibroblasts jcrb9067
A , C‐terminal of fibronectin (FBN‐C) turnover marker secretion by HK‐2 proximal tubular epithelial cells on HG and RAASi treatment. B , type IV collagen formation biomarker (PRO‐C4) secretion by HK‐2 cells on HG and RAASi treatment. C and D , PRO‐C4 secretion by <t>NRK‐49F</t> cells treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF; D ). Values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05 vs . control; §§ P < 0.01 vs . HG.
Nrk 49f Rat Renal Fibroblasts Jcrb9067, supplied by JCRB Cell Bank, 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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Image Search Results


Journal: eLife

Article Title: The spatial separation of processing and transport functions to the interior and periphery of the Golgi stack

doi: 10.7554/eLife.41301

Figure Lengend Snippet:

Article Snippet: Cell line ( Rattus norvegicus ) , Normal rat kidney (NRK) fibroblast cell , ATCC , ATCC: CRL-1570; RRID: CVCL_2144 , .

Techniques: Recombinant, Plasmid Preparation, Antibody Labeling, Software

Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal interstitial fibroblast NRK-49F. NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.

Journal: Journal of Cellular and Molecular Medicine

Article Title: Conditioned mesenchymal stem cells attenuate progression of chronic kidney disease through inhibition of epithelial-to-mesenchymal transition and immune modulation

doi: 10.1111/j.1582-4934.2012.01610.x

Figure Lengend Snippet: Effects of conditioned MSCs on expression of α-SMA and fibronectin in renal interstitial fibroblast NRK-49F. NRK-49F cells were cultured without or with 15 ng/ml TGF-β1 alone or co-culture with conditioned MSCs and/or ascorbic acid 2- phosphate for 3 days. ( A ) Representative Western blot analysis and relative bar graph analysis for α-SMA and β-tubulin level. ( B ) Representative Western blot and relative bar graph analysis of fibronectin protein level in NRK-49F after various treatments. * P < 0.05 versus normal control; ** P < 0.05 versus TGF-β1 treated.

Article Snippet: Rat renal proximal tubular cells (NRK-52E) and normal rat kidney interstitial fibroblast cells (NRK-49F) were purchased from the Bioresource Collection and Research Center of the Food Industry Research Institute, Taiwan.

Techniques: Expressing, Cell Culture, Co-Culture Assay, Western Blot, Control

A , C‐terminal of fibronectin (FBN‐C) turnover marker secretion by HK‐2 proximal tubular epithelial cells on HG and RAASi treatment. B , type IV collagen formation biomarker (PRO‐C4) secretion by HK‐2 cells on HG and RAASi treatment. C and D , PRO‐C4 secretion by NRK‐49F cells treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF; D ). Values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05 vs . control; §§ P < 0.01 vs . HG.

Journal: The Journal of Physiology

Article Title: RAAS inhibitors directly reduce diabetes‐induced renal fibrosis via growth factor inhibition

doi: 10.1113/JP277002

Figure Lengend Snippet: A , C‐terminal of fibronectin (FBN‐C) turnover marker secretion by HK‐2 proximal tubular epithelial cells on HG and RAASi treatment. B , type IV collagen formation biomarker (PRO‐C4) secretion by HK‐2 cells on HG and RAASi treatment. C and D , PRO‐C4 secretion by NRK‐49F cells treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF; D ). Values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05 vs . control; §§ P < 0.01 vs . HG.

Article Snippet: Human kidney 2 proximal tubular epithelial (HK‐2) cells (LGC Standards, ATCC Cat. No. CRL‐2190, RRID:CVCL_0302) were cultured in DMEM containing 5.5 mM glucose (Gibco, supplied by Life Technologies, Carlsbad, CA, USA) and normal rat kidney fibroblast (NRK‐49F) cells (LGC Standards, ATCC Cat. No. CRL‐1570, RRID:CVCL_2144) were maintained in DMEM containing 25 mM glucose (Gibco), both supplemented with 10% FBS (Gibco), 1% penicillin/streptomycin and 1% L‐glutamine, and incubated at 5% CO 2 and 37°C.

Techniques: Marker, Biomarker Assay, Derivative Assay

A , representative picture of platelet‐derived growth factor receptor β (PDGFR‐β) stained NRK‐49F cells. 1000× magnification; red, PDGFRβ; blue, nucleus; scale bar = 20 μm. B – D , representative pictures of phalloidin‐TRITC immunostained NRK‐49F cells (control, B ) treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF/CCN2; D ). 1000× magnification; red, F‐actin; blue, nucleus; scale bar = 20 μm. E and F , alpha‐smooth muscle actin (αSMA) protein levels in NRK‐49F cells treated with PDGF ( E ) or CTGF/CCN2r ( F ) and RAASi. Representative gel image examples shown above the panels. Samples might be from different gels but were derived at the same time and processed in parallel. On each graph values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05, *** P < 0.001 vs . control; § P < 0.05, §§§ P < 0.001 vs . PDGF or CTGF.

Journal: The Journal of Physiology

Article Title: RAAS inhibitors directly reduce diabetes‐induced renal fibrosis via growth factor inhibition

doi: 10.1113/JP277002

Figure Lengend Snippet: A , representative picture of platelet‐derived growth factor receptor β (PDGFR‐β) stained NRK‐49F cells. 1000× magnification; red, PDGFRβ; blue, nucleus; scale bar = 20 μm. B – D , representative pictures of phalloidin‐TRITC immunostained NRK‐49F cells (control, B ) treated with platelet‐derived growth factor (PDGF; C ) or connective tissue growth factor (CTGF/CCN2; D ). 1000× magnification; red, F‐actin; blue, nucleus; scale bar = 20 μm. E and F , alpha‐smooth muscle actin (αSMA) protein levels in NRK‐49F cells treated with PDGF ( E ) or CTGF/CCN2r ( F ) and RAASi. Representative gel image examples shown above the panels. Samples might be from different gels but were derived at the same time and processed in parallel. On each graph values are presented as means ± 95% confidence intervals; n = 6 wells/group; one‐way ANOVA followed by Bonferroniʹs multiple‐comparison post hoc test; * P < 0.05, *** P < 0.001 vs . control; § P < 0.05, §§§ P < 0.001 vs . PDGF or CTGF.

Article Snippet: Human kidney 2 proximal tubular epithelial (HK‐2) cells (LGC Standards, ATCC Cat. No. CRL‐2190, RRID:CVCL_0302) were cultured in DMEM containing 5.5 mM glucose (Gibco, supplied by Life Technologies, Carlsbad, CA, USA) and normal rat kidney fibroblast (NRK‐49F) cells (LGC Standards, ATCC Cat. No. CRL‐1570, RRID:CVCL_2144) were maintained in DMEM containing 25 mM glucose (Gibco), both supplemented with 10% FBS (Gibco), 1% penicillin/streptomycin and 1% L‐glutamine, and incubated at 5% CO 2 and 37°C.

Techniques: Derivative Assay, Staining