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human foreskin fibroblast (hff) normal cells lines  (Pasteur Institute)

 
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    Pasteur Institute human foreskin fibroblast (hff) normal cells lines
    Human Foreskin Fibroblast (Hff) Normal Cells Lines, supplied by Pasteur Institute, 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/normal+human+foreskin+fibroblasts+(hffs)+cell+line/human+foreskin+fibroblast++hff++cells/pm37715021-52-20-30
    Average 90 stars, based on 1 article reviews
    human foreskin fibroblast (hff) normal cells lines - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    MTT Assay:

    Article Title: Ferroptosis as a Potential Cell Death Mechanism Against Cisplatin-Resistant Lung Cancer Cell Line
    Article Snippet: The normal human foreskin fibroblasts (HFFs) cell line was purchased from the National Cell Bank Pasteur institute of Iran.

    Article Title: Synthesis and characterization of biocompatible ferrofluid based on magnetite nanoparticles and its effect on immunoglobulin G as an immune protein
    Article Snippet: Article history: Received 10 January 2018 Received in revised form 6 October 2018 Accepted 9 October 2018 Available online 12 October 2018 The investigation of interaction between protein fundamental to the immune system, immunoglobulin G (IgG), and superparamegnetic iron oxide nanoparticles (SPIONs) helps in designing the cell separation, drug delivery and hyperthermia systems.. For this reason, the superparamagnetic iron oxide nanoparticles (SPIONs) were prepared and coatedwith chitosan (CS) due to decrease of cytotoxicity.. The chitosan coated superparamegnetic iron oxide nanoparticles (CS-SPIONs)were characterized byX-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and the magnetic hyperthermia efficiency.

    Incubation:

    Article Title: Ferroptosis as a Potential Cell Death Mechanism Against Cisplatin-Resistant Lung Cancer Cell Line
    Article Snippet: The normal human foreskin fibroblasts (HFFs) cell line was purchased from the National Cell Bank Pasteur institute of Iran.

    Article Title: Synthesis and characterization of biocompatible ferrofluid based on magnetite nanoparticles and its effect on immunoglobulin G as an immune protein
    Article Snippet: Article history: Received 10 January 2018 Received in revised form 6 October 2018 Accepted 9 October 2018 Available online 12 October 2018 The investigation of interaction between protein fundamental to the immune system, immunoglobulin G (IgG), and superparamegnetic iron oxide nanoparticles (SPIONs) helps in designing the cell separation, drug delivery and hyperthermia systems.. For this reason, the superparamagnetic iron oxide nanoparticles (SPIONs) were prepared and coatedwith chitosan (CS) due to decrease of cytotoxicity.. The chitosan coated superparamegnetic iron oxide nanoparticles (CS-SPIONs)were characterized byX-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and the magnetic hyperthermia efficiency.

    Concentration Assay:

    Article Title: Ferroptosis as a Potential Cell Death Mechanism Against Cisplatin-Resistant Lung Cancer Cell Line
    Article Snippet: The normal human foreskin fibroblasts (HFFs) cell line was purchased from the National Cell Bank Pasteur institute of Iran.

    Article Title: Synthesis and characterization of biocompatible ferrofluid based on magnetite nanoparticles and its effect on immunoglobulin G as an immune protein
    Article Snippet: Article history: Received 10 January 2018 Received in revised form 6 October 2018 Accepted 9 October 2018 Available online 12 October 2018 The investigation of interaction between protein fundamental to the immune system, immunoglobulin G (IgG), and superparamegnetic iron oxide nanoparticles (SPIONs) helps in designing the cell separation, drug delivery and hyperthermia systems.. For this reason, the superparamagnetic iron oxide nanoparticles (SPIONs) were prepared and coatedwith chitosan (CS) due to decrease of cytotoxicity.. The chitosan coated superparamegnetic iron oxide nanoparticles (CS-SPIONs)were characterized byX-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and the magnetic hyperthermia efficiency.

    Flow Cytometry:

    Article Title: Ferroptosis as a Potential Cell Death Mechanism Against Cisplatin-Resistant Lung Cancer Cell Line
    Article Snippet: The normal human foreskin fibroblasts (HFFs) cell line was purchased from the National Cell Bank Pasteur institute of Iran.

    Article Title: Synthesis and characterization of biocompatible ferrofluid based on magnetite nanoparticles and its effect on immunoglobulin G as an immune protein
    Article Snippet: Article history: Received 10 January 2018 Received in revised form 6 October 2018 Accepted 9 October 2018 Available online 12 October 2018 The investigation of interaction between protein fundamental to the immune system, immunoglobulin G (IgG), and superparamegnetic iron oxide nanoparticles (SPIONs) helps in designing the cell separation, drug delivery and hyperthermia systems.. For this reason, the superparamagnetic iron oxide nanoparticles (SPIONs) were prepared and coatedwith chitosan (CS) due to decrease of cytotoxicity.. The chitosan coated superparamegnetic iron oxide nanoparticles (CS-SPIONs)were characterized byX-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and the magnetic hyperthermia efficiency.



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    Eriodictyol inhibited H 2 O 2 -induced cytotoxicity in dermal fibroblasts. ( A ) H 2 O 2 exposure (125–1000 µM; 1 h) resulted in a concentration-dependent decrease in the viability of BJ cells. ( B ) Eriodictyol treatment (10–40 µM; 24 h) did not result in cytotoxicity in BJ cells. ( C ) Eriodictyol pretreatment (10–40 µM; 24 h) prevented H 2 O 2 -induced cytotoxicity (500 µM; 1 h) in BJ cells. Cell viability was observed using the MTT assay after the indicated treatments. The survival percentage was calculated relative to untreated controls. DMSO (0.5%) was used as a vehicle control ( n = 3; each biological replicate consisted of four independent wells; mean ± SEM). * p < 0.05 versus vehicle controls ( A ) and p < 0.05 versus H 2 O 2 -treated cells ( C ). N.S. , not significant.

    Journal: Nutrients

    Article Title: Eriodictyol Attenuates H 2 O 2 -Induced Oxidative Damage in Human Dermal Fibroblasts through Enhanced Capacity of Antioxidant Machinery

    doi: 10.3390/nu14122553

    Figure Lengend Snippet: Eriodictyol inhibited H 2 O 2 -induced cytotoxicity in dermal fibroblasts. ( A ) H 2 O 2 exposure (125–1000 µM; 1 h) resulted in a concentration-dependent decrease in the viability of BJ cells. ( B ) Eriodictyol treatment (10–40 µM; 24 h) did not result in cytotoxicity in BJ cells. ( C ) Eriodictyol pretreatment (10–40 µM; 24 h) prevented H 2 O 2 -induced cytotoxicity (500 µM; 1 h) in BJ cells. Cell viability was observed using the MTT assay after the indicated treatments. The survival percentage was calculated relative to untreated controls. DMSO (0.5%) was used as a vehicle control ( n = 3; each biological replicate consisted of four independent wells; mean ± SEM). * p < 0.05 versus vehicle controls ( A ) and p < 0.05 versus H 2 O 2 -treated cells ( C ). N.S. , not significant.

    Article Snippet: Normal human foreskin fibroblast cell line BJ (ATCC No. CRL-2522) was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Concentration Assay, MTT Assay, Control

    Eriodictyol prevented the induction of necrosis in BJ cells following H 2 O 2 treatment. BJ cells were pre-treated with eriodictyol (5–20 µM; 24 h) followed by H 2 O 2 treatment (500 µM; 1h). After 24 h treatment with H 2 O 2 , dermal fibroblasts were co-stained with Hoechst 33342 (blue)/PI (red) to characterize mode of cell death ( n = 3; magnification = 20×; scale bar = 100 µm).

    Journal: Nutrients

    Article Title: Eriodictyol Attenuates H 2 O 2 -Induced Oxidative Damage in Human Dermal Fibroblasts through Enhanced Capacity of Antioxidant Machinery

    doi: 10.3390/nu14122553

    Figure Lengend Snippet: Eriodictyol prevented the induction of necrosis in BJ cells following H 2 O 2 treatment. BJ cells were pre-treated with eriodictyol (5–20 µM; 24 h) followed by H 2 O 2 treatment (500 µM; 1h). After 24 h treatment with H 2 O 2 , dermal fibroblasts were co-stained with Hoechst 33342 (blue)/PI (red) to characterize mode of cell death ( n = 3; magnification = 20×; scale bar = 100 µm).

    Article Snippet: Normal human foreskin fibroblast cell line BJ (ATCC No. CRL-2522) was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Staining