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sw48 human colorectal cancer cell lines  (ATCC)


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    Structured Review

    ATCC sw48 human colorectal cancer cell lines
    Sw48 Human Colorectal Cancer Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 817 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sw48 human colorectal cancer cell lines/product/ATCC
    Average 96 stars, based on 817 article reviews
    sw48 human colorectal cancer cell lines - by Bioz Stars, 2026-05
    96/100 stars

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    ATCC human crc cell lines sw48
    The analysis of overall survival ( A ), progression-free survival ( B ), disease-free survival ( C ), and disease-specific survival ( D ) analysis of patients with KRAS-WT and -mutant CRC based on the Cbioportal database. ( E ) The proportion of each mutation subtype in KRAS-mutant CRC. ( F ) The proportion of patients with KRAS-WT and -mutant patients in each subtype of CRC. ( G ) The mutation event frequency of various genes in KRAS-WT and -mutant CRC. ( H ) Differentially expressed genes in patients with KRAS-WT and -mutant CRC. ( I ) ART1 mRNA levels in KRAS-WT and -mutant CRC tissues. P < 0.05 by t test. ( J ) The positive intensity of ART1 in KRAS-WT and -mutant CRC tissues detected by immunohistochemistry. Original magnification, ×20 (top) and ×40 (bottom). ( K ) The expression of ART1 protein in KRAS-WT <t>(SW48,</t> Caco2, HT-29) and -mutant CRC cell lines (LoVo, HCT-116, SW480) observed by Western blot. Immunohistochemical detection of the expression of GRP78/BiP ( L ), HSC70 ( M ), and CHOP ( N ) in KRAS-WT and -mutant CRC tissues. Original magnification, ×200 (left) and ×400 (right). ( O ) The expression of GRP78/BiP, HSC70, and CHOP proteins in KRAS-WT and -mutant CRC cell lines detected by Western blot. ( P ) Transmission electron microscopy shows the morphology of the ER (arrows) in KRAS-WT and -mutant CRC cell lines. Original magnification, ×25,000.
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    ATCC human crc cell lines
    TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different <t>CRC</t> cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation <t>in</t> <t>HCT116</t> cells; overexpression of TMEM59L in <t>SW480</t> promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.
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    ATCC sw48 cell line
    TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different <t>CRC</t> cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation <t>in</t> <t>HCT116</t> cells; overexpression of TMEM59L in <t>SW480</t> promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.
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    ATCC cell line sw48
    TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different <t>CRC</t> cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation <t>in</t> <t>HCT116</t> cells; overexpression of TMEM59L in <t>SW480</t> promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.
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    ATCC human colon carcinoma cell lines
    TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different <t>CRC</t> cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation <t>in</t> <t>HCT116</t> cells; overexpression of TMEM59L in <t>SW480</t> promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.
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    ATCC human 119 colon adenocarcinoma cell line sw48
    TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different <t>CRC</t> cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation <t>in</t> <t>HCT116</t> cells; overexpression of TMEM59L in <t>SW480</t> promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.
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    Image Search Results


    The analysis of overall survival ( A ), progression-free survival ( B ), disease-free survival ( C ), and disease-specific survival ( D ) analysis of patients with KRAS-WT and -mutant CRC based on the Cbioportal database. ( E ) The proportion of each mutation subtype in KRAS-mutant CRC. ( F ) The proportion of patients with KRAS-WT and -mutant patients in each subtype of CRC. ( G ) The mutation event frequency of various genes in KRAS-WT and -mutant CRC. ( H ) Differentially expressed genes in patients with KRAS-WT and -mutant CRC. ( I ) ART1 mRNA levels in KRAS-WT and -mutant CRC tissues. P < 0.05 by t test. ( J ) The positive intensity of ART1 in KRAS-WT and -mutant CRC tissues detected by immunohistochemistry. Original magnification, ×20 (top) and ×40 (bottom). ( K ) The expression of ART1 protein in KRAS-WT (SW48, Caco2, HT-29) and -mutant CRC cell lines (LoVo, HCT-116, SW480) observed by Western blot. Immunohistochemical detection of the expression of GRP78/BiP ( L ), HSC70 ( M ), and CHOP ( N ) in KRAS-WT and -mutant CRC tissues. Original magnification, ×200 (left) and ×400 (right). ( O ) The expression of GRP78/BiP, HSC70, and CHOP proteins in KRAS-WT and -mutant CRC cell lines detected by Western blot. ( P ) Transmission electron microscopy shows the morphology of the ER (arrows) in KRAS-WT and -mutant CRC cell lines. Original magnification, ×25,000.

    Journal: JCI Insight

    Article Title: The critical role of GRP78/BiP MARylation in ER stress of KRAS-mutant colorectal cancer

    doi: 10.1172/jci.insight.182809

    Figure Lengend Snippet: The analysis of overall survival ( A ), progression-free survival ( B ), disease-free survival ( C ), and disease-specific survival ( D ) analysis of patients with KRAS-WT and -mutant CRC based on the Cbioportal database. ( E ) The proportion of each mutation subtype in KRAS-mutant CRC. ( F ) The proportion of patients with KRAS-WT and -mutant patients in each subtype of CRC. ( G ) The mutation event frequency of various genes in KRAS-WT and -mutant CRC. ( H ) Differentially expressed genes in patients with KRAS-WT and -mutant CRC. ( I ) ART1 mRNA levels in KRAS-WT and -mutant CRC tissues. P < 0.05 by t test. ( J ) The positive intensity of ART1 in KRAS-WT and -mutant CRC tissues detected by immunohistochemistry. Original magnification, ×20 (top) and ×40 (bottom). ( K ) The expression of ART1 protein in KRAS-WT (SW48, Caco2, HT-29) and -mutant CRC cell lines (LoVo, HCT-116, SW480) observed by Western blot. Immunohistochemical detection of the expression of GRP78/BiP ( L ), HSC70 ( M ), and CHOP ( N ) in KRAS-WT and -mutant CRC tissues. Original magnification, ×200 (left) and ×400 (right). ( O ) The expression of GRP78/BiP, HSC70, and CHOP proteins in KRAS-WT and -mutant CRC cell lines detected by Western blot. ( P ) Transmission electron microscopy shows the morphology of the ER (arrows) in KRAS-WT and -mutant CRC cell lines. Original magnification, ×25,000.

    Article Snippet: Human CRC cell lines SW48 (KRAS WT), HT-29 (KRAS WT), SW480 (G12V), and HCT116 (G13D) were obtained from American Type Culture Collection (ATCC).

    Techniques: Mutagenesis, Immunohistochemistry, Expressing, Western Blot, Immunohistochemical staining, Transmission Assay, Electron Microscopy

    TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different CRC cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation in HCT116 cells; overexpression of TMEM59L in SW480 promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.

    Journal: Cancer Reports

    Article Title: Transmembrane Protein TMEM59L Modulates 5‐ FU Resistance via PTPRN ‐Mediated DNA Damage Repair in Colorectal Cancer

    doi: 10.1002/cnr2.70448

    Figure Lengend Snippet: TMEM59L regulates colorectal cancer cells proliferation, migration, and invasion. (A) Western blotting confirmed expression of TMEM59L in different CRC cell lines. (B) Western blotting detects the knockdown of TMEM59L by shRNA and overexpression of TMEM59L by plasmid. (C) Downregulation of TMEM59L suppresses cell proliferation in HCT116 cells; overexpression of TMEM59L in SW480 promotes cell proliferation. (D) The function of TMEM59L on the migration and invasion ability of CRC cells was detected by Transwell assay. (E) E‐cadherin and Vimentin were evaluated through immunofluorescence staining in TMEM59L knockdown and overexpression CRC cells.

    Article Snippet: Five human CRC cell lines (NCI‐H716, HCT116, COLO 320DM, SW48, SW480) were sourced from the American Type Culture Collection (ATCC, USA), while a 5‐fluorouracil‐resistant HCT116 subline (HCT116/FU, BNCC342640) was obtained from BNCC (China).

    Techniques: Migration, Western Blot, Expressing, Knockdown, shRNA, Over Expression, Plasmid Preparation, Transwell Assay, Immunofluorescence, Staining

    TMEM59L was elevated in 5‐FU resistance CRC cell lines and reduced 5‐FU sensitivity. (A) The expression of TMEM59L in non‐responder and responder groups treated by 5‐FU ( n = 279 vs. 379, p = 0.0002), oxaliplatin ( n = 173 vs. 265, p = 0.012) and Capecitabine ( n = 62 vs. 47, p = 0.000019), respectively. (B) TMEM59L level in CRC cell lines and corresponding 5‐FU resistant cells was examined by western blot. (C, D) CCK‐8 assays of TMEM59L downregulation and upregulation on sensitivity of HCT116 and SW480 cells to 5‐FU; the half maximal inhibitory concentration (IC50) was calculated using GraphPad software. Data represent the mean ± SD ( n = 3), * p < 0.05 vs. HCT116 group, $ p < 0.05 vs. SW480 group.

    Journal: Cancer Reports

    Article Title: Transmembrane Protein TMEM59L Modulates 5‐ FU Resistance via PTPRN ‐Mediated DNA Damage Repair in Colorectal Cancer

    doi: 10.1002/cnr2.70448

    Figure Lengend Snippet: TMEM59L was elevated in 5‐FU resistance CRC cell lines and reduced 5‐FU sensitivity. (A) The expression of TMEM59L in non‐responder and responder groups treated by 5‐FU ( n = 279 vs. 379, p = 0.0002), oxaliplatin ( n = 173 vs. 265, p = 0.012) and Capecitabine ( n = 62 vs. 47, p = 0.000019), respectively. (B) TMEM59L level in CRC cell lines and corresponding 5‐FU resistant cells was examined by western blot. (C, D) CCK‐8 assays of TMEM59L downregulation and upregulation on sensitivity of HCT116 and SW480 cells to 5‐FU; the half maximal inhibitory concentration (IC50) was calculated using GraphPad software. Data represent the mean ± SD ( n = 3), * p < 0.05 vs. HCT116 group, $ p < 0.05 vs. SW480 group.

    Article Snippet: Five human CRC cell lines (NCI‐H716, HCT116, COLO 320DM, SW48, SW480) were sourced from the American Type Culture Collection (ATCC, USA), while a 5‐fluorouracil‐resistant HCT116 subline (HCT116/FU, BNCC342640) was obtained from BNCC (China).

    Techniques: Expressing, Western Blot, CCK-8 Assay, Concentration Assay, Software

    Silencing of TMEM59L enhanced DNA damage and 5‐FU sensibility in colorectal cancer cells and drug‐resistant CRC cell lines. (A, B) γ‐H2AX foci formation in HCT116 and SW480 cells was detected by immunofluorescence 48 h after treatment with 5‐FU (25 μg/mL). (C) Intracellular ROS levels in HCT116 and SW480 cells treated with 5‐FU for 48 h were detected by reactive oxygen species detection kit. (D) Effect of TMEM59L on apoptosis in CRC cells induced by 5‐FU (25 μg/mL) treatment for 48 h was determined by flow cytometric analysis. (E) Downregulation of TMEM59L reduced colony formation of HCT116/FU and SW480/FU cells.

    Journal: Cancer Reports

    Article Title: Transmembrane Protein TMEM59L Modulates 5‐ FU Resistance via PTPRN ‐Mediated DNA Damage Repair in Colorectal Cancer

    doi: 10.1002/cnr2.70448

    Figure Lengend Snippet: Silencing of TMEM59L enhanced DNA damage and 5‐FU sensibility in colorectal cancer cells and drug‐resistant CRC cell lines. (A, B) γ‐H2AX foci formation in HCT116 and SW480 cells was detected by immunofluorescence 48 h after treatment with 5‐FU (25 μg/mL). (C) Intracellular ROS levels in HCT116 and SW480 cells treated with 5‐FU for 48 h were detected by reactive oxygen species detection kit. (D) Effect of TMEM59L on apoptosis in CRC cells induced by 5‐FU (25 μg/mL) treatment for 48 h was determined by flow cytometric analysis. (E) Downregulation of TMEM59L reduced colony formation of HCT116/FU and SW480/FU cells.

    Article Snippet: Five human CRC cell lines (NCI‐H716, HCT116, COLO 320DM, SW48, SW480) were sourced from the American Type Culture Collection (ATCC, USA), while a 5‐fluorouracil‐resistant HCT116 subline (HCT116/FU, BNCC342640) was obtained from BNCC (China).

    Techniques: Immunofluorescence

    TMEM59L regulated 5‐FU induced DNA damage and ROS through PTPRN. (A) Physical interactions with TMEM59L in GeneMANIA website. (B) Correlation analysis between TMEM59L and PTPRN in COAD from GEPIA database. (C) PTPRN expression in COAD and READ from the TCGA database analyzed by the GEPIA database. (D) Higher PTPRN expression was related to poorer OS in CRC patients from TCGA through Kaplan–Meier Plotter database. (E) PTPRN partially reversed the effect of TMEM59L on 5‐FU induced ROS of HCT116 and SW480 cells. (F) PTPRN partially reversed the effect of TMEM59L on 5‐FU induced DNA damage of HCT116 and SW480 cells.

    Journal: Cancer Reports

    Article Title: Transmembrane Protein TMEM59L Modulates 5‐ FU Resistance via PTPRN ‐Mediated DNA Damage Repair in Colorectal Cancer

    doi: 10.1002/cnr2.70448

    Figure Lengend Snippet: TMEM59L regulated 5‐FU induced DNA damage and ROS through PTPRN. (A) Physical interactions with TMEM59L in GeneMANIA website. (B) Correlation analysis between TMEM59L and PTPRN in COAD from GEPIA database. (C) PTPRN expression in COAD and READ from the TCGA database analyzed by the GEPIA database. (D) Higher PTPRN expression was related to poorer OS in CRC patients from TCGA through Kaplan–Meier Plotter database. (E) PTPRN partially reversed the effect of TMEM59L on 5‐FU induced ROS of HCT116 and SW480 cells. (F) PTPRN partially reversed the effect of TMEM59L on 5‐FU induced DNA damage of HCT116 and SW480 cells.

    Article Snippet: Five human CRC cell lines (NCI‐H716, HCT116, COLO 320DM, SW48, SW480) were sourced from the American Type Culture Collection (ATCC, USA), while a 5‐fluorouracil‐resistant HCT116 subline (HCT116/FU, BNCC342640) was obtained from BNCC (China).

    Techniques: Expressing