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n1s1 rat hepatoma cells  (ATCC)


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    Structured Review

    ATCC n1s1 rat hepatoma cells
    In vivo MRI tracking of Gd-spores in an orthotopic liver tumor model. (A) In vivo experimental schedule for <t>N1S1</t> tumor implantation, intra-arterial administration of Gd-spores (10 8 /ml, prepared with 10 mM GdCl 3 ), and MRI. (B) Representative T1-weighted (T1W) and T2-weighted (T2W) MR images showing dynamic changes in tumor contrast following intra-arterial infusion of Gd-spores. (C) Tumor signal-to-noise ratio (SNR) and (D) contrast-to-noise ratio (CNR) on T1-weighted MR images up to 9 days ( n = 3). Data are presented as mean ± SD (* P < 0.05, *** P < 0.001, **** P < 0.0001).
    N1s1 Rat Hepatoma Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/n1s1 rat hepatoma cells/product/ATCC
    Average 93 stars, based on 23 article reviews
    n1s1 rat hepatoma cells - by Bioz Stars, 2026-06
    93/100 stars

    Images

    1) Product Images from "Metabolic Gadolinium Labeling of Clostridium novyi -Nontoxic for Magnetic Resonance Imaging Visualization of Spores and Germinated Bacteria"

    Article Title: Metabolic Gadolinium Labeling of Clostridium novyi -Nontoxic for Magnetic Resonance Imaging Visualization of Spores and Germinated Bacteria

    Journal: Biomaterials Research

    doi: 10.34133/bmr.0326

    In vivo MRI tracking of Gd-spores in an orthotopic liver tumor model. (A) In vivo experimental schedule for N1S1 tumor implantation, intra-arterial administration of Gd-spores (10 8 /ml, prepared with 10 mM GdCl 3 ), and MRI. (B) Representative T1-weighted (T1W) and T2-weighted (T2W) MR images showing dynamic changes in tumor contrast following intra-arterial infusion of Gd-spores. (C) Tumor signal-to-noise ratio (SNR) and (D) contrast-to-noise ratio (CNR) on T1-weighted MR images up to 9 days ( n = 3). Data are presented as mean ± SD (* P < 0.05, *** P < 0.001, **** P < 0.0001).
    Figure Legend Snippet: In vivo MRI tracking of Gd-spores in an orthotopic liver tumor model. (A) In vivo experimental schedule for N1S1 tumor implantation, intra-arterial administration of Gd-spores (10 8 /ml, prepared with 10 mM GdCl 3 ), and MRI. (B) Representative T1-weighted (T1W) and T2-weighted (T2W) MR images showing dynamic changes in tumor contrast following intra-arterial infusion of Gd-spores. (C) Tumor signal-to-noise ratio (SNR) and (D) contrast-to-noise ratio (CNR) on T1-weighted MR images up to 9 days ( n = 3). Data are presented as mean ± SD (* P < 0.05, *** P < 0.001, **** P < 0.0001).

    Techniques Used: In Vivo, Tumor Implantation



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    In vivo MRI tracking of Gd-spores in an orthotopic liver tumor model. (A) In vivo experimental schedule for <t>N1S1</t> tumor implantation, intra-arterial administration of Gd-spores (10 8 /ml, prepared with 10 mM GdCl 3 ), and MRI. (B) Representative T1-weighted (T1W) and T2-weighted (T2W) MR images showing dynamic changes in tumor contrast following intra-arterial infusion of Gd-spores. (C) Tumor signal-to-noise ratio (SNR) and (D) contrast-to-noise ratio (CNR) on T1-weighted MR images up to 9 days ( n = 3). Data are presented as mean ± SD (* P < 0.05, *** P < 0.001, **** P < 0.0001).
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    Dawley Inc rat hepatoma cell line n1s1 hepatoma cells
    Representative high-frequency ultrasound–based monitoring of orthotopic hepatocellular carcinoma established using the rat hepatoma cell line <t>(N1S1).</t> Tumor volume measurements obtained by ultrasound demonstrate an excellent correlation with reference histological and volumetric assessments ( r = 0.998, P < 0.001; Devan et al ), underscoring the accuracy, reproducibility, and experimental utility of this imaging approach for preclinical tumor evaluation. CT: Computed tomography; HCC: Hepatocellular carcinoma; 3D: Three dimensional; 3R: Replacement, reduction, and refinement. Created in BioRender ( www.biorender.com ).
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    ATCC n1s1 rat hepatoma cell line
    Changes in APT signal intensity (as a percentage) for the <t>N1S1</t> tumors following in LDL-OA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-OA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. Scale bar = 100 um.
    N1s1 Rat Hepatoma Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/n1s1 rat hepatoma cell line/product/ATCC
    Average 93 stars, based on 1 article reviews
    n1s1 rat hepatoma cell line - by Bioz Stars, 2026-06
    93/100 stars
      Buy from Supplier

    90
    Dawley Inc n1s1 rat hepatoma cells
    Changes in APT signal intensity (as a percentage) for the <t>N1S1</t> tumors following in LDL-OA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-OA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. Scale bar = 100 um.
    N1s1 Rat Hepatoma Cells, supplied by Dawley Inc, 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/result/n1s1 rat hepatoma cells/product/Dawley Inc
    Average 90 stars, based on 1 article reviews
    n1s1 rat hepatoma cells - by Bioz Stars, 2026-06
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    95
    ATCC rat hepatoma n1s1 cells
    Changes in APT signal intensity (as a percentage) for the <t>N1S1</t> tumors following in LDL-OA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-OA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. Scale bar = 100 um.
    Rat Hepatoma N1s1 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat hepatoma n1s1 cells/product/ATCC
    Average 95 stars, based on 1 article reviews
    rat hepatoma n1s1 cells - by Bioz Stars, 2026-06
    95/100 stars
      Buy from Supplier

    Image Search Results


    In vivo MRI tracking of Gd-spores in an orthotopic liver tumor model. (A) In vivo experimental schedule for N1S1 tumor implantation, intra-arterial administration of Gd-spores (10 8 /ml, prepared with 10 mM GdCl 3 ), and MRI. (B) Representative T1-weighted (T1W) and T2-weighted (T2W) MR images showing dynamic changes in tumor contrast following intra-arterial infusion of Gd-spores. (C) Tumor signal-to-noise ratio (SNR) and (D) contrast-to-noise ratio (CNR) on T1-weighted MR images up to 9 days ( n = 3). Data are presented as mean ± SD (* P < 0.05, *** P < 0.001, **** P < 0.0001).

    Journal: Biomaterials Research

    Article Title: Metabolic Gadolinium Labeling of Clostridium novyi -Nontoxic for Magnetic Resonance Imaging Visualization of Spores and Germinated Bacteria

    doi: 10.34133/bmr.0326

    Figure Lengend Snippet: In vivo MRI tracking of Gd-spores in an orthotopic liver tumor model. (A) In vivo experimental schedule for N1S1 tumor implantation, intra-arterial administration of Gd-spores (10 8 /ml, prepared with 10 mM GdCl 3 ), and MRI. (B) Representative T1-weighted (T1W) and T2-weighted (T2W) MR images showing dynamic changes in tumor contrast following intra-arterial infusion of Gd-spores. (C) Tumor signal-to-noise ratio (SNR) and (D) contrast-to-noise ratio (CNR) on T1-weighted MR images up to 9 days ( n = 3). Data are presented as mean ± SD (* P < 0.05, *** P < 0.001, **** P < 0.0001).

    Article Snippet: N1S1 rat hepatoma cells (ATCC CRL-1603) were cultured with Iscove’s Modified Dulbecco’s Medium, and 3 × 10 6 cells in 100 μl of phosphate-buffered saline (PBS) were inoculated in the left lateral lobe of the liver region of rats after the laparotomy.

    Techniques: In Vivo, Tumor Implantation

    Representative high-frequency ultrasound–based monitoring of orthotopic hepatocellular carcinoma established using the rat hepatoma cell line (N1S1). Tumor volume measurements obtained by ultrasound demonstrate an excellent correlation with reference histological and volumetric assessments ( r = 0.998, P < 0.001; Devan et al ), underscoring the accuracy, reproducibility, and experimental utility of this imaging approach for preclinical tumor evaluation. CT: Computed tomography; HCC: Hepatocellular carcinoma; 3D: Three dimensional; 3R: Replacement, reduction, and refinement. Created in BioRender ( www.biorender.com ).

    Journal: World Journal of Hepatology

    Article Title: Ultrasound imaging in orthotopic hepatocellular carcinoma models: Promise, practicality, and points for refinement

    doi: 10.4254/wjh.v17.i12.115551

    Figure Lengend Snippet: Representative high-frequency ultrasound–based monitoring of orthotopic hepatocellular carcinoma established using the rat hepatoma cell line (N1S1). Tumor volume measurements obtained by ultrasound demonstrate an excellent correlation with reference histological and volumetric assessments ( r = 0.998, P < 0.001; Devan et al ), underscoring the accuracy, reproducibility, and experimental utility of this imaging approach for preclinical tumor evaluation. CT: Computed tomography; HCC: Hepatocellular carcinoma; 3D: Three dimensional; 3R: Replacement, reduction, and refinement. Created in BioRender ( www.biorender.com ).

    Article Snippet: A syngeneic orthotopic HCC model was established in male Sprague Dawley rats by subcapsular implantation of the rat hepatoma cell line (N1S1) hepatoma cells into the left lateral liver lobe.

    Techniques: Imaging, Computed Tomography

    Changes in APT signal intensity (as a percentage) for the N1S1 tumors following in LDL-OA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-OA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. Scale bar = 100 um.

    Journal: Hepatic Oncology

    Article Title: APT imaging of hepatocellular carcinoma signals an effective therapeutic response in advance of tumor shrinkage

    doi: 10.1080/20450923.2024.2389031

    Figure Lengend Snippet: Changes in APT signal intensity (as a percentage) for the N1S1 tumors following in LDL-OA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-OA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. Scale bar = 100 um.

    Article Snippet: N1S1 rat hepatoma cell line (ATCC, CRL-1603, VA, USA) and the human liver tumor cell line HepG2 were cultured in Dulbecco's Modified Eagle's Medium (Sigma, D6429) supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin.

    Techniques: Staining

    Changes in APT signal intensity (as a percentage) for the N1S1 tumors following in LDL-DHA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-DHA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. *** represents p < 0.001 difference between groups. Scale bar = 100 um.

    Journal: Hepatic Oncology

    Article Title: APT imaging of hepatocellular carcinoma signals an effective therapeutic response in advance of tumor shrinkage

    doi: 10.1080/20450923.2024.2389031

    Figure Lengend Snippet: Changes in APT signal intensity (as a percentage) for the N1S1 tumors following in LDL-DHA nanoparticle treatment. (Upper panel) T 2 -weighted axial MRI (lower panel) APT imaged co-registered with T2 axial MRI. The ATP image masks are overlaid the liver and tumor region. (Insert upper) Change in the APT signal in liver and tumor tissue before, 24 and 72 h post LDL-DHA treatment. (Insert lower) H&E stained section showing liver and tumor interface. White arrows indicate tumor. *** represents p < 0.001 difference between groups. Scale bar = 100 um.

    Article Snippet: N1S1 rat hepatoma cell line (ATCC, CRL-1603, VA, USA) and the human liver tumor cell line HepG2 were cultured in Dulbecco's Modified Eagle's Medium (Sigma, D6429) supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin.

    Techniques: Staining