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hs68 primary human fetal foreskin fibroblast cells  (ATCC)


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    Structured Review

    ATCC hs68 primary human fetal foreskin fibroblast cells
    JP-1 inhibits the proliferation and colony formation of A549 cells but only slightly affects the growth of <t>HS68</t> primary <t>fibroblast</t> cells. (a) The cell viability of A549 cells after treatment with JP-1 for 72 h was measured by SRB binding assay. Data (mean ± SE) are expressed as a percentage compared to the control. (b) After 48 h of treatment, the effect of JP-1 on A549 cells was examined by phase-contrast microscopy, scale bar = 50 μ m. (c) Colonies formed by control and JP-1-treated A549 cells were assayed after 10 days of incubation. (d) Representative picture of colonies formed by the cells described in (c). Cell viability and colony formation data are expressed as mean ± SE and analyzed as described in .
    Hs68 Primary Human Fetal Foreskin Fibroblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 615 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hs68+primary+human+fetal+foreskin+fibroblast+cells/Hs68/pmc05203917-42-7-18
    Average 96 stars, based on 615 article reviews
    hs68 primary human fetal foreskin fibroblast cells - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells"

    Article Title: Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    doi: 10.1155/2016/5989681

    JP-1 inhibits the proliferation and colony formation of A549 cells but only slightly affects the growth of HS68 primary fibroblast cells. (a) The cell viability of A549 cells after treatment with JP-1 for 72 h was measured by SRB binding assay. Data (mean ± SE) are expressed as a percentage compared to the control. (b) After 48 h of treatment, the effect of JP-1 on A549 cells was examined by phase-contrast microscopy, scale bar = 50 μ m. (c) Colonies formed by control and JP-1-treated A549 cells were assayed after 10 days of incubation. (d) Representative picture of colonies formed by the cells described in (c). Cell viability and colony formation data are expressed as mean ± SE and analyzed as described in .
    Figure Legend Snippet: JP-1 inhibits the proliferation and colony formation of A549 cells but only slightly affects the growth of HS68 primary fibroblast cells. (a) The cell viability of A549 cells after treatment with JP-1 for 72 h was measured by SRB binding assay. Data (mean ± SE) are expressed as a percentage compared to the control. (b) After 48 h of treatment, the effect of JP-1 on A549 cells was examined by phase-contrast microscopy, scale bar = 50 μ m. (c) Colonies formed by control and JP-1-treated A549 cells were assayed after 10 days of incubation. (d) Representative picture of colonies formed by the cells described in (c). Cell viability and colony formation data are expressed as mean ± SE and analyzed as described in .

    Techniques Used: Binding Assay, Control, Microscopy, Incubation

    Related Articles

    Binding Assay:

    Article Title: Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells
    Article Snippet: The A549 human lung adenocarcinoma cells and HS68 primary human fetal foreskin fibroblast cells were purchased from the American Type Culture Collection (Manassas, VA, USA).. A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.

    Control:

    Article Title: Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells
    Article Snippet: The A549 human lung adenocarcinoma cells and HS68 primary human fetal foreskin fibroblast cells were purchased from the American Type Culture Collection (Manassas, VA, USA).. A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.

    Microscopy:

    Article Title: Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells
    Article Snippet: The A549 human lung adenocarcinoma cells and HS68 primary human fetal foreskin fibroblast cells were purchased from the American Type Culture Collection (Manassas, VA, USA).. A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.

    Incubation:

    Article Title: Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells
    Article Snippet: The A549 human lung adenocarcinoma cells and HS68 primary human fetal foreskin fibroblast cells were purchased from the American Type Culture Collection (Manassas, VA, USA).. A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.A549 cells were maintained in RPMI1640 and HS68 cells were in DMEM.



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    hs68 primary human fetal foreskin fibroblast cells  (ATCC)
    96
    ATCC hs68 primary human fetal foreskin fibroblast cells
    JP-1 inhibits the proliferation and colony formation of A549 cells but only slightly affects the growth of <t>HS68</t> primary <t>fibroblast</t> cells. (a) The cell viability of A549 cells after treatment with JP-1 for 72 h was measured by SRB binding assay. Data (mean ± SE) are expressed as a percentage compared to the control. (b) After 48 h of treatment, the effect of JP-1 on A549 cells was examined by phase-contrast microscopy, scale bar = 50 μ m. (c) Colonies formed by control and JP-1-treated A549 cells were assayed after 10 days of incubation. (d) Representative picture of colonies formed by the cells described in (c). Cell viability and colony formation data are expressed as mean ± SE and analyzed as described in .
    Hs68 Primary Human Fetal Foreskin Fibroblast Cells, 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
    https://www.bioz.com/product/hs68+primary+human+fetal+foreskin+fibroblast+cells/Hs68/pmc05203917-42-7-18
    Average 96 stars, based on 1 article reviews
    hs68 primary human fetal foreskin fibroblast cells - by Bioz Stars, 2026-09
    96/100 stars
    		  Buy from Supplier

    Image Search Results


    JP-1 inhibits the proliferation and colony formation of A549 cells but only slightly affects the growth of HS68 primary fibroblast cells. (a) The cell viability of A549 cells after treatment with JP-1 for 72 h was measured by SRB binding assay. Data (mean ± SE) are expressed as a percentage compared to the control. (b) After 48 h of treatment, the effect of JP-1 on A549 cells was examined by phase-contrast microscopy, scale bar = 50 μ m. (c) Colonies formed by control and JP-1-treated A549 cells were assayed after 10 days of incubation. (d) Representative picture of colonies formed by the cells described in (c). Cell viability and colony formation data are expressed as mean ± SE and analyzed as described in .

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocarcinoma Cells

    doi: 10.1155/2016/5989681

    Figure Lengend Snippet: JP-1 inhibits the proliferation and colony formation of A549 cells but only slightly affects the growth of HS68 primary fibroblast cells. (a) The cell viability of A549 cells after treatment with JP-1 for 72 h was measured by SRB binding assay. Data (mean ± SE) are expressed as a percentage compared to the control. (b) After 48 h of treatment, the effect of JP-1 on A549 cells was examined by phase-contrast microscopy, scale bar = 50 μ m. (c) Colonies formed by control and JP-1-treated A549 cells were assayed after 10 days of incubation. (d) Representative picture of colonies formed by the cells described in (c). Cell viability and colony formation data are expressed as mean ± SE and analyzed as described in .

    Article Snippet: The A549 human lung adenocarcinoma cells and HS68 primary human fetal foreskin fibroblast cells were purchased from the American Type Culture Collection (Manassas, VA, USA).

    Techniques: Binding Assay, Control, Microscopy, Incubation