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ln18 glioma cells  (ATCC)


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    ATCC ln18 glioma cells
    Ln18 Glioma Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 791 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ln18+glioma+cells/LN-18/pm41817895-62-2-18
    Average 96 stars, based on 791 article reviews
    ln18 glioma cells - by Bioz Stars, 2026-09
    96/100 stars

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    Derivative Assay:

    Article Title: MGMT downregulation by CRISPR/Cas13 RNA-guided RNA targeting enhances glioma cell sensitivity to TMZ chemotherapy.
    Article Snippet: Purified RNA was used to synthesize first-strand cDNA (SuperScriptTM III Reverse Transcriptase, Invitrogen) and the remaining MGMT transcript was measured by PCR using the REDTaq® ReadyMIX PCR Reaction Kit (Sigma-Aldrich) and MGMT-specific primers (Forward: 5’- T G C G C A C C G T T T G C G A C T T G-3’; Reverse: 5’- G G T T G C C T G C C A G G G C T G C-3’). .. Culture of LN18 glioma cells and patient derived glioma stem-like cells (gliomaspheres) LN18 glioma cells were sourced from American Type Culture Collection (Manassas, Virginia) and primary patientderived GS104 and GS081 gliomaspheres were supplied by Dr. Nathanson (Department of Molecular and Medical Pharmacology, UCLA). ..



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    FIGURE 1 PMA and glioma cells stimulated neutrophils to release NETs. (A) Neutrophils were stimulated with PMA for 1, 2, 3, and 4 h, respectively, and then stained with Sytox Green (green) and Hoechst 33342 (blue) to observe NETs (scale: 50 μm). (B) Quantitative results of fluorescent staining of the area of PMA-stimulated neutrophils releasing NETs at different time points (ns = not statistically significant, **p < 0.01, ***p < 0.001). (C) PMA stimulation of neutrophils for 4 h, and immunofluorescence staining of both citH3 (green) and DNA (DAPI, blue) was performed to visualize NETs, the white arrows indicate NETs (scale bar: 20 μm). (D) Fluorescence-stained images of <t>LN18</t> CM stimulated neutrophils for 4 h to release NETs (scale bar: 50 μm). (E) Quantitative results of fluorescence staining of the area of LN18 CM-stimulated neutrophils releasing NETs at 4 h (****p < 0.0001). (F) Immunofluorescence staining images of LN18 CM-stimulated neutrophils releasing NETs at 4 h, the white arrows indicate NETs (scale bar: 20 μm). Error bars in B and E represent SD.
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    FIGURE 1 PMA and glioma cells stimulated neutrophils to release NETs. (A) Neutrophils were stimulated with PMA for 1, 2, 3, and 4 h, respectively, and then stained with Sytox Green (green) and Hoechst 33342 (blue) to observe NETs (scale: 50 μm). (B) Quantitative results of fluorescent staining of the area of PMA-stimulated neutrophils releasing NETs at different time points (ns = not statistically significant, **p < 0.01, ***p < 0.001). (C) PMA stimulation of neutrophils for 4 h, and immunofluorescence staining of both citH3 (green) and DNA (DAPI, blue) was performed to visualize NETs, the white arrows indicate NETs (scale bar: 20 μm). (D) Fluorescence-stained images of <t>LN18</t> CM stimulated neutrophils for 4 h to release NETs (scale bar: 50 μm). (E) Quantitative results of fluorescence staining of the area of LN18 CM-stimulated neutrophils releasing NETs at 4 h (****p < 0.0001). (F) Immunofluorescence staining images of LN18 CM-stimulated neutrophils releasing NETs at 4 h, the white arrows indicate NETs (scale bar: 20 μm). Error bars in B and E represent SD.
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    FIGURE 1 PMA and glioma cells stimulated neutrophils to release NETs. (A) Neutrophils were stimulated with PMA for 1, 2, 3, and 4 h, respectively, and then stained with Sytox Green (green) and Hoechst 33342 (blue) to observe NETs (scale: 50 μm). (B) Quantitative results of fluorescent staining of the area of PMA-stimulated neutrophils releasing NETs at different time points (ns = not statistically significant, **p < 0.01, ***p < 0.001). (C) PMA stimulation of neutrophils for 4 h, and immunofluorescence staining of both citH3 (green) and DNA (DAPI, blue) was performed to visualize NETs, the white arrows indicate NETs (scale bar: 20 μm). (D) Fluorescence-stained images of <t>LN18</t> CM stimulated neutrophils for 4 h to release NETs (scale bar: 50 μm). (E) Quantitative results of fluorescence staining of the area of LN18 CM-stimulated neutrophils releasing NETs at 4 h (****p < 0.0001). (F) Immunofluorescence staining images of LN18 CM-stimulated neutrophils releasing NETs at 4 h, the white arrows indicate NETs (scale bar: 20 μm). Error bars in B and E represent SD.
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    Image Search Results


    Fig. 1. The expression of adiponectin receptor in the LN18 glioma cell line.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 1. The expression of adiponectin receptor in the LN18 glioma cell line.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Expressing

    Fig. 2. Effect of adiponectin on LN18 glioma cell proliferation. (a) Dose-dependent relationship of adiponectin on the proliferation of LN18 glioma cells; (b) Time-dependent relationship of adiponectin on the proliferation of LN18 glioma cells. Compared with the control group, *P < 0.05.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 2. Effect of adiponectin on LN18 glioma cell proliferation. (a) Dose-dependent relationship of adiponectin on the proliferation of LN18 glioma cells; (b) Time-dependent relationship of adiponectin on the proliferation of LN18 glioma cells. Compared with the control group, *P < 0.05.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Control

    Fig. 4. Adiponectin regulates the expression of apoptosis-related pro teins in LN18 cells. Compared with the control group, *P<0.05.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 4. Adiponectin regulates the expression of apoptosis-related pro teins in LN18 cells. Compared with the control group, *P<0.05.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Expressing, Control

    Fig. 5. Effect of adiponectin on apoptosis of LN18 glioma cells. (a) Control group; (b) Adiponectin 0.5 μg/mL; (c) Adiponectin 1.0 μg/ mL; (d) Adiponectin 3.0 μg/mL.Compared with the control group, *P<0.05.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 5. Effect of adiponectin on apoptosis of LN18 glioma cells. (a) Control group; (b) Adiponectin 0.5 μg/mL; (c) Adiponectin 1.0 μg/ mL; (d) Adiponectin 3.0 μg/mL.Compared with the control group, *P<0.05.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Control

    Fig. 6. Adiponectin regulates the expression of LN18 cell cycle-rela ted proteins. Compared with the control group, *P<0.05.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 6. Adiponectin regulates the expression of LN18 cell cycle-rela ted proteins. Compared with the control group, *P<0.05.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Expressing, Control

    Fig. 7. Effect of adiponectin on LN18 cell proliferation. (a) Control group, (b) Adiponectin 3.0 μg/mL. Compared with the control group, *P<0.05.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 7. Effect of adiponectin on LN18 cell proliferation. (a) Control group, (b) Adiponectin 3.0 μg/mL. Compared with the control group, *P<0.05.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Control

    Fig. 8. Effect of adiponectin on the expression of autophagy-related proteins in LN18 cells. Compared with the control group, *P<0.05.

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 8. Effect of adiponectin on the expression of autophagy-related proteins in LN18 cells. Compared with the control group, *P<0.05.

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Expressing, Control

    Fig. 9. Adiponectin enhances the inhibitory effect of TMZ on the pro liferation rate of the LN18 cell line. Compared with the control group and excipient group, *P<0.05; compared with TMZ 1.0 mM group,

    Journal: Cellular and molecular biology (Noisy-le-Grand, France)

    Article Title: Regulation and molecular mechanism of adiponectin on the proliferation, apoptosis, autophagy, and chemosensitivity of LN18 Glioma cell line.

    doi: 10.14715/cmb/2024.70.6.27

    Figure Lengend Snippet: Fig. 9. Adiponectin enhances the inhibitory effect of TMZ on the pro liferation rate of the LN18 cell line. Compared with the control group and excipient group, *P<0.05; compared with TMZ 1.0 mM group,

    Article Snippet: Gliomas cell lines LN18, U87MG, and U251 cells were obtained from the American Type Culture Collection (ATCC), thawed from early-passage stocks kept in liquid nitrogen vapor as required, and cultured according to the supplier’s instructions.

    Techniques: Control

    FIGURE 1 PMA and glioma cells stimulated neutrophils to release NETs. (A) Neutrophils were stimulated with PMA for 1, 2, 3, and 4 h, respectively, and then stained with Sytox Green (green) and Hoechst 33342 (blue) to observe NETs (scale: 50 μm). (B) Quantitative results of fluorescent staining of the area of PMA-stimulated neutrophils releasing NETs at different time points (ns = not statistically significant, **p < 0.01, ***p < 0.001). (C) PMA stimulation of neutrophils for 4 h, and immunofluorescence staining of both citH3 (green) and DNA (DAPI, blue) was performed to visualize NETs, the white arrows indicate NETs (scale bar: 20 μm). (D) Fluorescence-stained images of LN18 CM stimulated neutrophils for 4 h to release NETs (scale bar: 50 μm). (E) Quantitative results of fluorescence staining of the area of LN18 CM-stimulated neutrophils releasing NETs at 4 h (****p < 0.0001). (F) Immunofluorescence staining images of LN18 CM-stimulated neutrophils releasing NETs at 4 h, the white arrows indicate NETs (scale bar: 20 μm). Error bars in B and E represent SD.

    Journal: Cancer medicine

    Article Title: Biomarkers of peripheral blood neutrophil extracellular traps in the diagnosis and progression of malignant tumors.

    doi: 10.1002/cam4.6935

    Figure Lengend Snippet: FIGURE 1 PMA and glioma cells stimulated neutrophils to release NETs. (A) Neutrophils were stimulated with PMA for 1, 2, 3, and 4 h, respectively, and then stained with Sytox Green (green) and Hoechst 33342 (blue) to observe NETs (scale: 50 μm). (B) Quantitative results of fluorescent staining of the area of PMA-stimulated neutrophils releasing NETs at different time points (ns = not statistically significant, **p < 0.01, ***p < 0.001). (C) PMA stimulation of neutrophils for 4 h, and immunofluorescence staining of both citH3 (green) and DNA (DAPI, blue) was performed to visualize NETs, the white arrows indicate NETs (scale bar: 20 μm). (D) Fluorescence-stained images of LN18 CM stimulated neutrophils for 4 h to release NETs (scale bar: 50 μm). (E) Quantitative results of fluorescence staining of the area of LN18 CM-stimulated neutrophils releasing NETs at 4 h (****p < 0.0001). (F) Immunofluorescence staining images of LN18 CM-stimulated neutrophils releasing NETs at 4 h, the white arrows indicate NETs (scale bar: 20 μm). Error bars in B and E represent SD.

    Article Snippet: The human glioma cell line LN18 (American Type Culture Collection, USA) was cultured in DMEM medium (Gibco, USA) containing 5% fetal bovine serum and 1% penicillin– streptomycin.

    Techniques: Staining, Immunofluorescence, Fluorescence