normal human foreskin fibroblast cells nhf Search Results


mrc 5  (ATCC)
99
ATCC mrc 5
Mrc 5, 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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ccd 27sk  (ATCC)
93
ATCC ccd 27sk
Ccd 27sk, 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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primary dermal fibroblast normal; human, neonatal  (ATCC)
98
ATCC primary dermal fibroblast normal; human, neonatal
Primary Dermal Fibroblast Normal; Human, Neonatal, supplied by ATCC, 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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primary dermal fibroblast; normal, human, adult  (ATCC)
99
ATCC primary dermal fibroblast; normal, human, adult
Primary Dermal Fibroblast; Normal, Human, Adult, 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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primary dermal fibroblast; normal, human, adult - by Bioz Stars, 2026-03
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primary gingival fibroblast; normal, human, adult  (ATCC)
99
ATCC primary gingival fibroblast; normal, human, adult
Primary Gingival Fibroblast; Normal, Human, Adult, 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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normal human fibroblast (nhf) cell lines  (Coriell Institute for Medical Research)
90
Coriell Institute for Medical Research normal human fibroblast (nhf) cell lines
Normal Human Fibroblast (Nhf) Cell Lines, supplied by Coriell Institute for Medical Research, 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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normal human fibroblast cells crl1554  (ATCC)
93
ATCC normal human fibroblast cells crl1554
Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells <t>(CRL1554)</t> (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.
Normal Human Fibroblast Cells Crl1554, 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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normal human fibroblast cells crl1554 - by Bioz Stars, 2026-03
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non-fetal human skinfibroblasts (nhf)  (Coriell Institute for Medical Research)
90
Coriell Institute for Medical Research non-fetal human skinfibroblasts (nhf)
Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells <t>(CRL1554)</t> (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.
Non Fetal Human Skinfibroblasts (Nhf), supplied by Coriell Institute for Medical Research, 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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normal human fibroblast cell lines  (ATCC)
96
ATCC normal human fibroblast cell lines
Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells <t>(CRL1554)</t> (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.
Normal Human Fibroblast Cell Lines, 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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primary lung fibroblast, normal, human  (ATCC)
99
ATCC primary lung fibroblast, normal, human
Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells <t>(CRL1554)</t> (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.
Primary Lung Fibroblast, Normal, Human, 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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celltiter-glo  (Promega)
90
Promega celltiter-glo
Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells <t>(CRL1554)</t> (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.
Celltiter Glo, supplied by Promega, 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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ws1 normal human fibroblast cell line  (ATCC)
96
ATCC ws1 normal human fibroblast cell line
Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells <t>(CRL1554)</t> (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.
Ws1 Normal Human Fibroblast Cell Line, 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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Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells (CRL1554) (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.

Journal: Cancer Cell International

Article Title: Growth inhibitory and chemo-sensitization effects of naringenin, a natural flavanone purified from Thymus vulgaris , on human breast and colorectal cancer

doi: 10.1186/s12935-015-0194-0

Figure Lengend Snippet: Time and dose-dependent anti-proliferative effects and inhibition of colony formation of Nar on human colorectal and breast cancer cell lines. Human colorectal cancer cells (SW1116, SW837) (A a- e) , human breast cancer cells (HTB 26, HTB132) (B a- e) and normal human fibroblast cells (CRL1554) (A, B a- e) were plated (27 × 10 3 cells/well) in 96-well plates in CO 2 and non-CO 2 incubators, depending on type of media and cells, at 37°C for 18 h. The cells were then treated with various concentrations of Nar (0.05 – 4.0 mM) for 3–24 h. Cell growth was monitored using an MTT assay. Untreated and Nar-treated colorectal cancer cells SW1116 (Ca) , SW837 (Cb) and Nar-treated breast cancer cells HTB26 (Cc) , HTB132 (Cd) were trypsinized, counted and plated (500 cells /well) in 6-well plates. Following 10–14 days of incubation in non-CO 2 incubator at 37°C, the colonies were fixed and stained with crystal violet. The stained colonies were counted and compared with the untreated control.

Article Snippet: Human colorectal cancer cell lines (SW1116 and SW837), human breast cancer cell lines (HTB26, HTB132), and normal human fibroblast cells (CRL1554) were obtained from American Type Culture Collection (ATCC; VA, USA).

Techniques: Inhibition, MTT Assay, Incubation, Staining, Control