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cell culture human normal fibroblast bj cells  (ATCC)
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ATCC cell culture human normal fibroblast bj cells
Cell Culture Human Normal Fibroblast Bj Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bj normal human foreskin primary fibroblast cell line  (ATCC)
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TGC and/or unloaded CD NPs ameliorated the S. Typhimurium infected group induced histopathological alterations in mice’s liver tissues. Representative photomicrographs of the H&E-stained hepatic tissue sections showing the control (A), S. Typhimurium infected group (C), TGC (E), unloaded CD NPs (G), CD-TGC groups (I) and their respective higher magnifications (B, D, F, H, and J). A, B: control group displaying normal central vein (CV), hepatic cords (HC) with hepatocytes of eosinophilic granular cytoplasm (EC), rounded central single (SN) or double vesicular nuclei (DN), and kupffer cells (KC). C, D: S. Typhimurium infected group demonstrating multiple areas of variable-sized necrotic areas (NA) of coagulative necrosis (CN), severely dilated and congested sinusoid (SDS) with Kupffer cell hyperplasia (KCH). E, F: TGC group displaying moderately sized necrotic areas (MNA), moderately dilated and congested sinusoids (MDS), moderately hyperplastic Kupffer’s cells (MKC), interstitial mononuclear cell infiltration (MI), <t>fibroblast</t> proliferation (FP), and regenerated hepatocytes of stippling basophilic cytoplasm (BC) and pale nuclei (PN). G, H: unloaded CD NPs group showing a few scattered minute necrotic areas (mNA), intense mononuclear cell infiltration (IMI) around the portal area, and apparently normal hepatocytes (NH). I, J: CD-TGC group showed normal hepatocytes (NH), few dilated blood vessels (DBV), and a few interstitial lymphocytic aggregates (FL). Scale bars = 100 μm in A, C, E, G, I; and = 20 μm in B, D, F, H, and J. K: Bar charts demonstrate the statistical analysis of the comparative quantification of the hepatic injury scores in all studied groups. Bars carrying different superscript letters (a, b, c, d, and e) are significantly different as analyzed by the one-way ANOVA test, followed by the multiple comparisons by Duncan’s Post-hoc test ( p < 0.05). Values are the mean of 6 mice per group ± S.E.M.
Bj Normal Human Foreskin Primary Fibroblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bj normal human foreskin primary fibroblast cell line - by Bioz Stars, 2026-09
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bj normal human fibroplasts bj normal human foreskin primary fibroblast cell line  (ATCC)
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TGC and/or unloaded CD NPs ameliorated the S. Typhimurium infected group induced histopathological alterations in mice’s liver tissues. Representative photomicrographs of the H&E-stained hepatic tissue sections showing the control (A), S. Typhimurium infected group (C), TGC (E), unloaded CD NPs (G), CD-TGC groups (I) and their respective higher magnifications (B, D, F, H, and J). A, B: control group displaying normal central vein (CV), hepatic cords (HC) with hepatocytes of eosinophilic granular cytoplasm (EC), rounded central single (SN) or double vesicular nuclei (DN), and kupffer cells (KC). C, D: S. Typhimurium infected group demonstrating multiple areas of variable-sized necrotic areas (NA) of coagulative necrosis (CN), severely dilated and congested sinusoid (SDS) with Kupffer cell hyperplasia (KCH). E, F: TGC group displaying moderately sized necrotic areas (MNA), moderately dilated and congested sinusoids (MDS), moderately hyperplastic Kupffer’s cells (MKC), interstitial mononuclear cell infiltration (MI), <t>fibroblast</t> proliferation (FP), and regenerated hepatocytes of stippling basophilic cytoplasm (BC) and pale nuclei (PN). G, H: unloaded CD NPs group showing a few scattered minute necrotic areas (mNA), intense mononuclear cell infiltration (IMI) around the portal area, and apparently normal hepatocytes (NH). I, J: CD-TGC group showed normal hepatocytes (NH), few dilated blood vessels (DBV), and a few interstitial lymphocytic aggregates (FL). Scale bars = 100 μm in A, C, E, G, I; and = 20 μm in B, D, F, H, and J. K: Bar charts demonstrate the statistical analysis of the comparative quantification of the hepatic injury scores in all studied groups. Bars carrying different superscript letters (a, b, c, d, and e) are significantly different as analyzed by the one-way ANOVA test, followed by the multiple comparisons by Duncan’s Post-hoc test ( p < 0.05). Values are the mean of 6 mice per group ± S.E.M.
Bj Normal Human Fibroplasts Bj Normal Human Foreskin Primary Fibroblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine <t>fibroblast</t> L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).
Primary Human Dermal Fibroblast Bj Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine <t>fibroblast</t> L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).
Normal Skin Fibroblast Cell Bj, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine <t>fibroblast</t> L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).
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Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine <t>fibroblast</t> L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).
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Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine <t>fibroblast</t> L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).
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TGC and/or unloaded CD NPs ameliorated the S. Typhimurium infected group induced histopathological alterations in mice’s liver tissues. Representative photomicrographs of the H&E-stained hepatic tissue sections showing the control (A), S. Typhimurium infected group (C), TGC (E), unloaded CD NPs (G), CD-TGC groups (I) and their respective higher magnifications (B, D, F, H, and J). A, B: control group displaying normal central vein (CV), hepatic cords (HC) with hepatocytes of eosinophilic granular cytoplasm (EC), rounded central single (SN) or double vesicular nuclei (DN), and kupffer cells (KC). C, D: S. Typhimurium infected group demonstrating multiple areas of variable-sized necrotic areas (NA) of coagulative necrosis (CN), severely dilated and congested sinusoid (SDS) with Kupffer cell hyperplasia (KCH). E, F: TGC group displaying moderately sized necrotic areas (MNA), moderately dilated and congested sinusoids (MDS), moderately hyperplastic Kupffer’s cells (MKC), interstitial mononuclear cell infiltration (MI), fibroblast proliferation (FP), and regenerated hepatocytes of stippling basophilic cytoplasm (BC) and pale nuclei (PN). G, H: unloaded CD NPs group showing a few scattered minute necrotic areas (mNA), intense mononuclear cell infiltration (IMI) around the portal area, and apparently normal hepatocytes (NH). I, J: CD-TGC group showed normal hepatocytes (NH), few dilated blood vessels (DBV), and a few interstitial lymphocytic aggregates (FL). Scale bars = 100 μm in A, C, E, G, I; and = 20 μm in B, D, F, H, and J. K: Bar charts demonstrate the statistical analysis of the comparative quantification of the hepatic injury scores in all studied groups. Bars carrying different superscript letters (a, b, c, d, and e) are significantly different as analyzed by the one-way ANOVA test, followed by the multiple comparisons by Duncan’s Post-hoc test ( p < 0.05). Values are the mean of 6 mice per group ± S.E.M.

Journal: Scientific Reports

Article Title: Chitosan-dextran sulfate nanocapsules for enhanced tigecycline efficacy against non-typhoidal Salmonella enterica

doi: 10.1038/s41598-026-35229-7

Figure Lengend Snippet: TGC and/or unloaded CD NPs ameliorated the S. Typhimurium infected group induced histopathological alterations in mice’s liver tissues. Representative photomicrographs of the H&E-stained hepatic tissue sections showing the control (A), S. Typhimurium infected group (C), TGC (E), unloaded CD NPs (G), CD-TGC groups (I) and their respective higher magnifications (B, D, F, H, and J). A, B: control group displaying normal central vein (CV), hepatic cords (HC) with hepatocytes of eosinophilic granular cytoplasm (EC), rounded central single (SN) or double vesicular nuclei (DN), and kupffer cells (KC). C, D: S. Typhimurium infected group demonstrating multiple areas of variable-sized necrotic areas (NA) of coagulative necrosis (CN), severely dilated and congested sinusoid (SDS) with Kupffer cell hyperplasia (KCH). E, F: TGC group displaying moderately sized necrotic areas (MNA), moderately dilated and congested sinusoids (MDS), moderately hyperplastic Kupffer’s cells (MKC), interstitial mononuclear cell infiltration (MI), fibroblast proliferation (FP), and regenerated hepatocytes of stippling basophilic cytoplasm (BC) and pale nuclei (PN). G, H: unloaded CD NPs group showing a few scattered minute necrotic areas (mNA), intense mononuclear cell infiltration (IMI) around the portal area, and apparently normal hepatocytes (NH). I, J: CD-TGC group showed normal hepatocytes (NH), few dilated blood vessels (DBV), and a few interstitial lymphocytic aggregates (FL). Scale bars = 100 μm in A, C, E, G, I; and = 20 μm in B, D, F, H, and J. K: Bar charts demonstrate the statistical analysis of the comparative quantification of the hepatic injury scores in all studied groups. Bars carrying different superscript letters (a, b, c, d, and e) are significantly different as analyzed by the one-way ANOVA test, followed by the multiple comparisons by Duncan’s Post-hoc test ( p < 0.05). Values are the mean of 6 mice per group ± S.E.M.

Article Snippet: BJ normal human foreskin primary fibroblast cell line (ATCC CRL-2522) was used for studying safety of CD-TGC nanocapsules.

Techniques: Infection, Staining, Control

Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine fibroblast L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).

Journal: International Journal of Molecular Sciences

Article Title: Green-Synthesized MgO Nanoparticles: Structural Insights and Antimicrobial Applications

doi: 10.3390/ijms26189021

Figure Lengend Snippet: Cytotoxicity assessment of green-synthesized MgO NPs after 4 days of incubation for ( a , c ) murine fibroblast L929 cells and ( b , d ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).

Article Snippet: Immortalized murine fibroblast L929 cells, primary human dermal fibroblast BJ cells (both from the American Type Culture Collection, ATCC, Manassas, VA, USA), and MG-63 osteoblast-like cells (Cell Lines Service GmbH, Heidelberg, Germany) were cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% Penicillin–Streptomycin antibiotic solution to assess cell viability and prepare cell cultures.

Techniques: Synthesized, Incubation, Negative Control

Cytotoxicity assessment of green-synthesized MgO NPs after 7 days of incubation for ( a ) murine fibroblast L929 cells and ( b ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).

Journal: International Journal of Molecular Sciences

Article Title: Green-Synthesized MgO Nanoparticles: Structural Insights and Antimicrobial Applications

doi: 10.3390/ijms26189021

Figure Lengend Snippet: Cytotoxicity assessment of green-synthesized MgO NPs after 7 days of incubation for ( a ) murine fibroblast L929 cells and ( b ) MG-63 osteoblast-like cells. The negative control consisted of cells incubated only with complete culture medium. Data are expressed as mean ± SD. Statistical analysis was performed using Student’s t -test (* p < 0.05, ** p ≤ 0.01, *** p ≤ 0.001).

Article Snippet: Immortalized murine fibroblast L929 cells, primary human dermal fibroblast BJ cells (both from the American Type Culture Collection, ATCC, Manassas, VA, USA), and MG-63 osteoblast-like cells (Cell Lines Service GmbH, Heidelberg, Germany) were cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% Penicillin–Streptomycin antibiotic solution to assess cell viability and prepare cell cultures.

Techniques: Synthesized, Incubation, Negative Control