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cell culture 65 human oscc cell lines scc9  (ATCC)


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    ATCC cell culture 65 human oscc cell lines scc9
    Cell Culture 65 Human Oscc Cell Lines Scc9, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1152 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cell culture 65 human oscc cell lines scc9/product/ATCC
    Average 97 stars, based on 1152 article reviews
    cell culture 65 human oscc cell lines scc9 - by Bioz Stars, 2026-03
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    ATCC cell culture human oscc cell lines cal27
    (a) Molecular structure of the EDB-FN-specific contrast agent MT218. (b-d) Immunohistochemical staining of EDB-FN in human tissues with the EDB-FN-specific G4 antibody was (b) weak in normal tongue specimens (n=3), (c) strong in untreated primary <t>OSCC</t> specimens (n=7), (d) strong in OSCC metastatic specimens (n=2), and (e) moderate in neoadjuvant primary OSCC specimens (n=3). Scale bars in all panels: 200 μm.
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    https://www.bioz.com/result/cell culture human oscc cell lines cal27/product/ATCC
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    ATCC cell culture human oscc cal27 cells
    (a) Molecular structure of the EDB-FN-specific contrast agent MT218. (b-d) Immunohistochemical staining of EDB-FN in human tissues with the EDB-FN-specific G4 antibody was (b) weak in normal tongue specimens (n=3), (c) strong in untreated primary <t>OSCC</t> specimens (n=7), (d) strong in OSCC metastatic specimens (n=2), and (e) moderate in neoadjuvant primary OSCC specimens (n=3). Scale bars in all panels: 200 μm.
    Cell Culture Human Oscc Cal27 Cells, 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
    https://www.bioz.com/result/cell culture human oscc cal27 cells/product/ATCC
    Average 99 stars, based on 1 article reviews
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    Image Search Results


    (a) Molecular structure of the EDB-FN-specific contrast agent MT218. (b-d) Immunohistochemical staining of EDB-FN in human tissues with the EDB-FN-specific G4 antibody was (b) weak in normal tongue specimens (n=3), (c) strong in untreated primary OSCC specimens (n=7), (d) strong in OSCC metastatic specimens (n=2), and (e) moderate in neoadjuvant primary OSCC specimens (n=3). Scale bars in all panels: 200 μm.

    Journal: Molecular imaging and biology

    Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

    doi: 10.1007/s11307-020-01524-6

    Figure Lengend Snippet: (a) Molecular structure of the EDB-FN-specific contrast agent MT218. (b-d) Immunohistochemical staining of EDB-FN in human tissues with the EDB-FN-specific G4 antibody was (b) weak in normal tongue specimens (n=3), (c) strong in untreated primary OSCC specimens (n=7), (d) strong in OSCC metastatic specimens (n=2), and (e) moderate in neoadjuvant primary OSCC specimens (n=3). Scale bars in all panels: 200 μm.

    Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Immunohistochemical staining, Staining

    (a) qRT-PCR mRNA analysis (n=3) and (b) western blot protein analysis (n=3) revealed differential and upregulated expression of EDB-FN in aggressive HSC3 and SCC4 cells. (c) Peptide binding study of spheroids with EDB-FN-specific ZD2-Cy5.5 (n=3) showed strong staining in HSC3 and SCC4 spheroids, but not CAL27 spheroids. Quantification of confocal images revealed (d) larger spheroids and (e) stronger ZD2-Cy5.5 staining in HSC3 and SCC4 spheroids in accordance with their EDB-FN expression levels. Data was analyzed with One-Way ANOVA and Fisher’s least significant difference post-hoc tests (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05). Scale bars for confocal images: 200 μm.

    Journal: Molecular imaging and biology

    Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

    doi: 10.1007/s11307-020-01524-6

    Figure Lengend Snippet: (a) qRT-PCR mRNA analysis (n=3) and (b) western blot protein analysis (n=3) revealed differential and upregulated expression of EDB-FN in aggressive HSC3 and SCC4 cells. (c) Peptide binding study of spheroids with EDB-FN-specific ZD2-Cy5.5 (n=3) showed strong staining in HSC3 and SCC4 spheroids, but not CAL27 spheroids. Quantification of confocal images revealed (d) larger spheroids and (e) stronger ZD2-Cy5.5 staining in HSC3 and SCC4 spheroids in accordance with their EDB-FN expression levels. Data was analyzed with One-Way ANOVA and Fisher’s least significant difference post-hoc tests (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05). Scale bars for confocal images: 200 μm.

    Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Quantitative RT-PCR, Western Blot, Expressing, Binding Assay, Staining

    (a) Cells grown in 2D and 3D culture (n=3) showed high-risk features in HSC3 and SCC4 cells, but not CAL27 cells. (b) Transwell migration and invasion assays (n=3) demonstrated high invasive potential of HSC3 and SCC4 cells, but not CAL27 cells. Scale bars in all panels: 400 μm.

    Journal: Molecular imaging and biology

    Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

    doi: 10.1007/s11307-020-01524-6

    Figure Lengend Snippet: (a) Cells grown in 2D and 3D culture (n=3) showed high-risk features in HSC3 and SCC4 cells, but not CAL27 cells. (b) Transwell migration and invasion assays (n=3) demonstrated high invasive potential of HSC3 and SCC4 cells, but not CAL27 cells. Scale bars in all panels: 400 μm.

    Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Migration

    CNR analysis of contrast-enhanced tumors revealed (a) significant differential enhancement between CAL27, HSC3, and SCC4 tumors with MT218 in accordance with their EDB-FN expression, while (b) gadoteridol showed no difference in enhancement between the three models. Enhancement with MT218 was (c) generally lower than gadoteridol in CAL27 tumors, (d) generally higher than gadoteridol in HSC3 tumors, and (e) substantially higher than gadoteridol in SCC4 tumors. Maximum CNR enhancement in subjects with MT218 was (f) borderline lower than gadoteridol in CAL27 tumors (p=0.0957), (g) borderline higher than gadoteridol in HSC3 tumors (p=0.0639), and (h) significantly higher than gadoteridol in SCC4 tumors. (f-h) Open dots connected with a solid line represent matched mouse-by-mouse data, and solid dots connected with a dotted line represent cohort averages. (i) Average maximum CNR enhancement was significantly different between the three tumor models in accordance with their EDB-FN expression with MT218, but not with gadoteridol. Data was analyzed with Two-Way ANOVA and Fisher’s least significant difference post-hoc test (a-e,i) and unpaired T-tests (f-h) (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05).

    Journal: Molecular imaging and biology

    Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

    doi: 10.1007/s11307-020-01524-6

    Figure Lengend Snippet: CNR analysis of contrast-enhanced tumors revealed (a) significant differential enhancement between CAL27, HSC3, and SCC4 tumors with MT218 in accordance with their EDB-FN expression, while (b) gadoteridol showed no difference in enhancement between the three models. Enhancement with MT218 was (c) generally lower than gadoteridol in CAL27 tumors, (d) generally higher than gadoteridol in HSC3 tumors, and (e) substantially higher than gadoteridol in SCC4 tumors. Maximum CNR enhancement in subjects with MT218 was (f) borderline lower than gadoteridol in CAL27 tumors (p=0.0957), (g) borderline higher than gadoteridol in HSC3 tumors (p=0.0639), and (h) significantly higher than gadoteridol in SCC4 tumors. (f-h) Open dots connected with a solid line represent matched mouse-by-mouse data, and solid dots connected with a dotted line represent cohort averages. (i) Average maximum CNR enhancement was significantly different between the three tumor models in accordance with their EDB-FN expression with MT218, but not with gadoteridol. Data was analyzed with Two-Way ANOVA and Fisher’s least significant difference post-hoc test (a-e,i) and unpaired T-tests (f-h) (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05).

    Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Expressing

    (a) CAL27 tumors (n=5 for pre, 10, 20, and 30 minutes, n=4 for 40 minutes) showed slightly less enhancement with MT218 than gadoteridol. (b) HSC3 tumors (n=4) showed slightly more enhancement with MT218 than gadoteridol. (c) SCC4 tumors (n=4) showed substantially more enhancement with MT218 than gadoteridol. MT218 and gadoteridol were used at doses of 0.04 mmol/kg and 0.10 mmol/kg, respectively.

    Journal: Molecular imaging and biology

    Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

    doi: 10.1007/s11307-020-01524-6

    Figure Lengend Snippet: (a) CAL27 tumors (n=5 for pre, 10, 20, and 30 minutes, n=4 for 40 minutes) showed slightly less enhancement with MT218 than gadoteridol. (b) HSC3 tumors (n=4) showed slightly more enhancement with MT218 than gadoteridol. (c) SCC4 tumors (n=4) showed substantially more enhancement with MT218 than gadoteridol. MT218 and gadoteridol were used at doses of 0.04 mmol/kg and 0.10 mmol/kg, respectively.

    Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques:

    (a) H&E staining of OSCC xenografts (n=3) showed various morphological features and stages of differentiation. (b) Immunohistochemistry for EDB-FN with the EDB-FN-specific G4 antibody (n=3) showed weak, moderate and strong staining in the epithelial regions of CAL27, HSC3, and SCC4 tumors, respectively, with little nonspecific staining. Scale bars: 600μm for H&E images, 200μm for immunohistochemistry images.

    Journal: Molecular imaging and biology

    Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

    doi: 10.1007/s11307-020-01524-6

    Figure Lengend Snippet: (a) H&E staining of OSCC xenografts (n=3) showed various morphological features and stages of differentiation. (b) Immunohistochemistry for EDB-FN with the EDB-FN-specific G4 antibody (n=3) showed weak, moderate and strong staining in the epithelial regions of CAL27, HSC3, and SCC4 tumors, respectively, with little nonspecific staining. Scale bars: 600μm for H&E images, 200μm for immunohistochemistry images.

    Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Staining, Immunohistochemistry