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normal human lung fibroblasts  (ATCC)


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    ATCC normal human lung fibroblasts
    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung <t>fibroblasts</t> <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
    Normal Human Lung Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 65 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 65 article reviews
    normal human lung fibroblasts - by Bioz Stars, 2026-05
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    Images

    1) Product Images from "Machine Learning Optimization of Laser Ablation in Liquid for the Green and Low-Cost Synthesis of Clean Gold Nanoparticles"

    Article Title: Machine Learning Optimization of Laser Ablation in Liquid for the Green and Low-Cost Synthesis of Clean Gold Nanoparticles

    Journal: Journal of the American Chemical Society

    doi: 10.1021/jacs.6c02047

    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts (CCD-34Lu, J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
    Figure Legend Snippet: (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts (CCD-34Lu, J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.

    Techniques Used: Comparison, MTS Assay, Incubation



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    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung <t>fibroblasts</t> <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
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    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung <t>fibroblasts</t> <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
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    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
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    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
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    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
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    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts <t>(CCD-34Lu,</t> J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.
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    Image Search Results


    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts (CCD-34Lu, J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.

    Journal: Journal of the American Chemical Society

    Article Title: Machine Learning Optimization of Laser Ablation in Liquid for the Green and Low-Cost Synthesis of Clean Gold Nanoparticles

    doi: 10.1021/jacs.6c02047

    Figure Lengend Snippet: (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts (CCD-34Lu, J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.

    Article Snippet: Human Umbilical Vein Endothelial Cells (HUVECs) and normal human lung fibroblasts (CCD-34Lu) were obtained from the ATCC.

    Techniques: Comparison, MTS Assay, Incubation

    (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts (CCD-34Lu, J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.

    Journal: Journal of the American Chemical Society

    Article Title: Machine Learning Optimization of Laser Ablation in Liquid for the Green and Low-Cost Synthesis of Clean Gold Nanoparticles

    doi: 10.1021/jacs.6c02047

    Figure Lengend Snippet: (A) UV–vis absorption spectra of LAL and CS Au NPs after coating with MUA. Spectra were normalized at 400 nm for easier comparison. XPS analysis of S 2p (B) and Au 4f (C) peaks in LAL (black) and CS (blue) Au NP samples. Catalytic reduction of 4-NP with NaBH 4 by LAL (D) and CS (E) Au NPs is indicated by the gradual reduction of the 4-NP band at 400 nm, while that of 4-AP at 230 nm increases. (F) The comparison of the pseudo-first-order kinetic model fitting of all samples shows the superior performance of the LAL Au NPs. MALDI spectra of three low-mass analytes, l -arginine (MW 174.20, G), l -asparagine (MW 132.12, H), and atrazine (MW 215.68, I), were recorded using three different matrices: LAL Au NPs (black), CS Au NPs (blue), and HCCA (green). The cytotoxicity of LAL and CS Au NPs was assessed by using the MTS assay in normal lung fibroblasts (CCD-34Lu, J) and human endothelial cells (HUVEC, K) for an incubation period of 48 h.

    Article Snippet: CCD-34Lu fibroblasts were maintained in RPMI-1640 Medium, ATCC modification (Thermo Fisher Scientific), supplemented with 10% fetal bovine serum (FBS; Thermo Fisher Scientific).

    Techniques: Comparison, MTS Assay, Incubation