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human foreskin fibroblast cell line  (ATCC)


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    ATCC human foreskin fibroblast cell line
    Human Foreskin Fibroblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 620 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/foreskin+fibroblast+crl+1635+cell+lines/Hs68/pm41677530-190-2-8
    Average 96 stars, based on 620 article reviews
    human foreskin fibroblast cell line - by Bioz Stars, 2026-10
    96/100 stars

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    other:

    Article Title: Colostrum-Derived Exosomal Lactoferrin Promotes Skin Fibroblast Regeneration by Suppressing Inflammatory Responses
    Article Snippet: The mouse 3T3/NIH embryo fibroblast (CRL-1658) and human HS-68 new foreskin fibroblast (CRL-1635) cell lines were purchased from the American Type Culture Collection (Manassas, VA, USA).

    Article Title: Colostrum-Derived Exosomal Lactoferrin Promotes Skin Fibroblast Regeneration by Suppressing Inflammatory Responses
    Article Snippet: The mouse 3T3/NIH embryo fibroblast (CRL-1658) and human HS-68 new foreskin fibroblast (CRL-1635) cell lines were purchased from the American Type Culture Collection (Manassas, VA, USA).



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    human foreskin fibroblast cell line  (ATCC)
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    human foreskin fibroblast cell line hs68  (ATCC)
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    ATCC human foreskin fibroblast cell line hs68
    Fig. 5. Cell viability (%) of <t>Hs68</t> (A) Jurkat (B) and MOLT-4 (C) cells after being treated with His6-fPS2, MBP-fPS2, and MBP-tPS2 at different concentrations. The proteinase K-treated and non-proteinase K-treated samples are denoted as + ProK and – ProK, respectively. Cell viability (%) of Jurkat (D) and MOLT-4 (E) in response to non-proteinase K-treated MBP-fPS2 and MBP-tPS2 treatments at different concentrations. After 24 h of incubation with various concentrations of protein samples, the percentage of cell viability was determined by MTT assay by comparing the absorbance of each sample to that of the negative control (PBS, pH 7.4). All data are presented as mean ± SD from the triplicate analyses. Statistical significance was analyzed using two-way ANOVA and annotated as follows: **** p < 0.0001, *** p < 0.001, ns (no significance) p > 0.9.
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    Fig. 5. Cell viability (%) of Hs68 (A) Jurkat (B) and MOLT-4 (C) cells after being treated with His6-fPS2, MBP-fPS2, and MBP-tPS2 at different concentrations. The proteinase K-treated and non-proteinase K-treated samples are denoted as + ProK and – ProK, respectively. Cell viability (%) of Jurkat (D) and MOLT-4 (E) in response to non-proteinase K-treated MBP-fPS2 and MBP-tPS2 treatments at different concentrations. After 24 h of incubation with various concentrations of protein samples, the percentage of cell viability was determined by MTT assay by comparing the absorbance of each sample to that of the negative control (PBS, pH 7.4). All data are presented as mean ± SD from the triplicate analyses. Statistical significance was analyzed using two-way ANOVA and annotated as follows: **** p < 0.0001, *** p < 0.001, ns (no significance) p > 0.9.

    Journal: Biotechnology reports (Amsterdam, Netherlands)

    Article Title: A fusion protein designed for soluble expression, rapid purification, and enhanced stability of parasporin-2 with potential therapeutic applications.

    doi: 10.1016/j.btre.2024.e00851

    Figure Lengend Snippet: Fig. 5. Cell viability (%) of Hs68 (A) Jurkat (B) and MOLT-4 (C) cells after being treated with His6-fPS2, MBP-fPS2, and MBP-tPS2 at different concentrations. The proteinase K-treated and non-proteinase K-treated samples are denoted as + ProK and – ProK, respectively. Cell viability (%) of Jurkat (D) and MOLT-4 (E) in response to non-proteinase K-treated MBP-fPS2 and MBP-tPS2 treatments at different concentrations. After 24 h of incubation with various concentrations of protein samples, the percentage of cell viability was determined by MTT assay by comparing the absorbance of each sample to that of the negative control (PBS, pH 7.4). All data are presented as mean ± SD from the triplicate analyses. Statistical significance was analyzed using two-way ANOVA and annotated as follows: **** p < 0.0001, *** p < 0.001, ns (no significance) p > 0.9.

    Article Snippet: Human foreskin fibroblast cell line Hs68 (ATCC CRL-1635), T-acute lymphoblastic leukemia cells lines: MOLT-4 (ATCC CRL-1582) and Jurkat (ATCC TIB-152T) were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Incubation, MTT Assay, Negative Control