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human glioma cell lines hs683  (ATCC)


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    ATCC human glioma cell lines hs683
    Human Glioma Cell Lines Hs683, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 377 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human glioma cell lines hs683/product/ATCC
    Average 95 stars, based on 377 article reviews
    human glioma cell lines hs683 - by Bioz Stars, 2026-05
    95/100 stars

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    ATCC human glioma cell lines hs683
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    ATCC hs683 cell lines
    Expression of SLC16A1 in SW1088 and <t>HS683</t> after transfection with si-SLC16A1. A The expressions of LDHA and SLC16A1 in low-grade glioma cell lines. The X-axis represented different cells, while the Y-axis represented the relative expression of LDHA and SLC16A1. Control, normal human glial cells; Low-grade glioma cell lines SW1088 and HS683. **, P < 0.01, when compared with control. B The mRNA expression of SLC16A1 was detected by qRT-PCR. C The protein expression of SLC16A1 was detected by western blot. Protein concentrations were determined by BCA assay, and equal amounts (30 µg) were loaded in each lane.***, P < 0.001
    Hs683 Cell Lines, 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
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    ATCC hs683 htb 138 human oligodendroglioma cell line
    Knockdown of spermine synthase (SMS) inhibits the malignant behavior of lower-grade glioma cells. A : Western blot analysis of SMS protein expression levels in human normal glial cell lines CP-H121/122/123 and glioma cell line <t>HS683/U251,</t> with statistical analysis on the right. B : The efficiency of SMS knockdown in HS683/U251 glioma cell line detected by Western blot, with protein expression analysis on the right. C : The efficiency of SMS knockdown in HS683/U251 glioma cell line detected by quantitative reverse transcription polymerase chain reaction. D : Cell proliferation before and after SMS knockdown was measured by CCK-8 assay. E : The apoptosis ratio of cells before and after SMS knockdown was measured by flow cytometry, with statistical analysis on the right. F : Several cell clones formed before and after SMS knockdown, with statistical results. G : Migration of cells before and after SMS knockdown measured by scratch wound healing assay. H : Migration and invasive ability of cells before and after SMS knockdown measured by transwell assay. NC : normal control. *** p <0.001.
    Hs683 Htb 138 Human Oligodendroglioma Cell Line, 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
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    ATCC human glioma cell line hs683
    Association between EIF4E and PBK and patient survival. The co-expression relationship between EIF4E and PBK was performed by the cBioPortal online platform (A). The expression of EIF4E was downregulated after PBK knockdown in <t>HS683</t> (B). GEPIA online platform was used to perform the expression of EIF4E in glioma and its effect on survival. EIF4E mRNA expression in GBM compared to normal brain tissues (C) in which normal samples are marked in gray and GBM samples are marked in red. High EIF4E expression decreases both overall survival (D) and disease-free survival (E).
    Human Glioma Cell Line Hs683, 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
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    Procell Inc hs683 cell line
    Association between EIF4E and PBK and patient survival. The co-expression relationship between EIF4E and PBK was performed by the cBioPortal online platform (A). The expression of EIF4E was downregulated after PBK knockdown in <t>HS683</t> (B). GEPIA online platform was used to perform the expression of EIF4E in glioma and its effect on survival. EIF4E mRNA expression in GBM compared to normal brain tissues (C) in which normal samples are marked in gray and GBM samples are marked in red. High EIF4E expression decreases both overall survival (D) and disease-free survival (E).
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    Procell Inc hs683 human glioma cell line
    ( A ) The qRT-PCR assays validated the siRNA knockdown effect. ( B ) The results of CCK-8 assay in <t>HS683</t> cell lines. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.
    Hs683 Human Glioma Cell Line, supplied by Procell Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Genechem human representative glioma cell lines u87mg, u251, a172, hs683
    ( A ) The qRT-PCR assays validated the siRNA knockdown effect. ( B ) The results of CCK-8 assay in <t>HS683</t> cell lines. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.
    Human Representative Glioma Cell Lines U87mg, U251, A172, Hs683, supplied by Genechem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Expression of SLC16A1 in SW1088 and HS683 after transfection with si-SLC16A1. A The expressions of LDHA and SLC16A1 in low-grade glioma cell lines. The X-axis represented different cells, while the Y-axis represented the relative expression of LDHA and SLC16A1. Control, normal human glial cells; Low-grade glioma cell lines SW1088 and HS683. **, P < 0.01, when compared with control. B The mRNA expression of SLC16A1 was detected by qRT-PCR. C The protein expression of SLC16A1 was detected by western blot. Protein concentrations were determined by BCA assay, and equal amounts (30 µg) were loaded in each lane.***, P < 0.001

    Journal: Discover Oncology

    Article Title: Identification and validation of LDHA and SLC16A1 for predicting prognosis and diagnosis in lower-grade glioma

    doi: 10.1007/s12672-025-03297-2

    Figure Lengend Snippet: Expression of SLC16A1 in SW1088 and HS683 after transfection with si-SLC16A1. A The expressions of LDHA and SLC16A1 in low-grade glioma cell lines. The X-axis represented different cells, while the Y-axis represented the relative expression of LDHA and SLC16A1. Control, normal human glial cells; Low-grade glioma cell lines SW1088 and HS683. **, P < 0.01, when compared with control. B The mRNA expression of SLC16A1 was detected by qRT-PCR. C The protein expression of SLC16A1 was detected by western blot. Protein concentrations were determined by BCA assay, and equal amounts (30 µg) were loaded in each lane.***, P < 0.001

    Article Snippet: The LGG cell lines of SW1088 and HS683 cell lines were obtained from the American Type Culture Collection (ATCC, USA).

    Techniques: Expressing, Transfection, Control, Quantitative RT-PCR, Western Blot, BIA-KA

    Low expression of SLC16A1 inhibits glioma cell proliferation, migration, and invasion. A Proliferation curve of SW1088 cells. B Proliferation curve of HS683 cells. C Transwell assay was used to detect the migration ability of SW1088 and HS683 cells (×100). D Transwell assay was used to detect the invasion ability of SW1088 and HS683 cells (×100). *, P < 0.05, **, P < 0.01, ***, P < 0.001

    Journal: Discover Oncology

    Article Title: Identification and validation of LDHA and SLC16A1 for predicting prognosis and diagnosis in lower-grade glioma

    doi: 10.1007/s12672-025-03297-2

    Figure Lengend Snippet: Low expression of SLC16A1 inhibits glioma cell proliferation, migration, and invasion. A Proliferation curve of SW1088 cells. B Proliferation curve of HS683 cells. C Transwell assay was used to detect the migration ability of SW1088 and HS683 cells (×100). D Transwell assay was used to detect the invasion ability of SW1088 and HS683 cells (×100). *, P < 0.05, **, P < 0.01, ***, P < 0.001

    Article Snippet: The LGG cell lines of SW1088 and HS683 cell lines were obtained from the American Type Culture Collection (ATCC, USA).

    Techniques: Expressing, Migration, Transwell Assay

    Knockdown of spermine synthase (SMS) inhibits the malignant behavior of lower-grade glioma cells. A : Western blot analysis of SMS protein expression levels in human normal glial cell lines CP-H121/122/123 and glioma cell line HS683/U251, with statistical analysis on the right. B : The efficiency of SMS knockdown in HS683/U251 glioma cell line detected by Western blot, with protein expression analysis on the right. C : The efficiency of SMS knockdown in HS683/U251 glioma cell line detected by quantitative reverse transcription polymerase chain reaction. D : Cell proliferation before and after SMS knockdown was measured by CCK-8 assay. E : The apoptosis ratio of cells before and after SMS knockdown was measured by flow cytometry, with statistical analysis on the right. F : Several cell clones formed before and after SMS knockdown, with statistical results. G : Migration of cells before and after SMS knockdown measured by scratch wound healing assay. H : Migration and invasive ability of cells before and after SMS knockdown measured by transwell assay. NC : normal control. *** p <0.001.

    Journal: Journal of Korean Neurosurgical Society

    Article Title: Spermine Synthase : A Potential Prognostic Marker for Lower-Grade Gliomas

    doi: 10.3340/jkns.2024.0080

    Figure Lengend Snippet: Knockdown of spermine synthase (SMS) inhibits the malignant behavior of lower-grade glioma cells. A : Western blot analysis of SMS protein expression levels in human normal glial cell lines CP-H121/122/123 and glioma cell line HS683/U251, with statistical analysis on the right. B : The efficiency of SMS knockdown in HS683/U251 glioma cell line detected by Western blot, with protein expression analysis on the right. C : The efficiency of SMS knockdown in HS683/U251 glioma cell line detected by quantitative reverse transcription polymerase chain reaction. D : Cell proliferation before and after SMS knockdown was measured by CCK-8 assay. E : The apoptosis ratio of cells before and after SMS knockdown was measured by flow cytometry, with statistical analysis on the right. F : Several cell clones formed before and after SMS knockdown, with statistical results. G : Migration of cells before and after SMS knockdown measured by scratch wound healing assay. H : Migration and invasive ability of cells before and after SMS knockdown measured by transwell assay. NC : normal control. *** p <0.001.

    Article Snippet: The HS683 (HTB-138) human oligodendroglioma cell line and the U251 (HTB-17) glioblastoma cell line were obtained from ATCC (Manassas, VA, USA).

    Techniques: Knockdown, Western Blot, Expressing, Reverse Transcription, Polymerase Chain Reaction, CCK-8 Assay, Flow Cytometry, Clone Assay, Migration, Wound Healing Assay, Transwell Assay, Control

    Association between EIF4E and PBK and patient survival. The co-expression relationship between EIF4E and PBK was performed by the cBioPortal online platform (A). The expression of EIF4E was downregulated after PBK knockdown in HS683 (B). GEPIA online platform was used to perform the expression of EIF4E in glioma and its effect on survival. EIF4E mRNA expression in GBM compared to normal brain tissues (C) in which normal samples are marked in gray and GBM samples are marked in red. High EIF4E expression decreases both overall survival (D) and disease-free survival (E).

    Journal: Annals of Medicine and Surgery

    Article Title: Unraveling the role of PBK in glioblastoma: from molecular mechanisms to therapeutic targets

    doi: 10.1097/MS9.0000000000002708

    Figure Lengend Snippet: Association between EIF4E and PBK and patient survival. The co-expression relationship between EIF4E and PBK was performed by the cBioPortal online platform (A). The expression of EIF4E was downregulated after PBK knockdown in HS683 (B). GEPIA online platform was used to perform the expression of EIF4E in glioma and its effect on survival. EIF4E mRNA expression in GBM compared to normal brain tissues (C) in which normal samples are marked in gray and GBM samples are marked in red. High EIF4E expression decreases both overall survival (D) and disease-free survival (E).

    Article Snippet: The human glioma cell line HS683 was obtained from the American Type Culture Collection (ATCC) and cultured according to ATCC instructions in DMEM medium with 10% FBS in a 5% CO 2 incubator at 37°C. shRNA sequences for PBK knockdown and cell line establishment were based on a previous study .

    Techniques: Expressing, Knockdown

    ( A ) The qRT-PCR assays validated the siRNA knockdown effect. ( B ) The results of CCK-8 assay in HS683 cell lines. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.

    Journal: Scientific Reports

    Article Title: Stemness subtypes in lower-grade glioma with prognostic biomarkers, tumor microenvironment, and treatment response

    doi: 10.1038/s41598-024-65717-7

    Figure Lengend Snippet: ( A ) The qRT-PCR assays validated the siRNA knockdown effect. ( B ) The results of CCK-8 assay in HS683 cell lines. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.

    Article Snippet: The HS683 human glioma cell line was sourced from Wuhan Procell Life Science and Technology Co., Ltd. (Procell, China).

    Techniques: Quantitative RT-PCR, Knockdown, CCK-8 Assay

    Scratch wound healing assessment of HS683 cell lines following treatment with siRNA or negative control (NC) targeting four hub genes: ( A ) CDCA8, ( B ) DLGAP5, ( C ) ORC1 and ( D ) SMC4. Transwell examination of LGG cell lines treated with siRNA or negative control (NC) to target four hub genes: ( E ) CDCA8, ( F ) DLGAP5, ( G ) ORC1 and ( H ) SMC4. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.

    Journal: Scientific Reports

    Article Title: Stemness subtypes in lower-grade glioma with prognostic biomarkers, tumor microenvironment, and treatment response

    doi: 10.1038/s41598-024-65717-7

    Figure Lengend Snippet: Scratch wound healing assessment of HS683 cell lines following treatment with siRNA or negative control (NC) targeting four hub genes: ( A ) CDCA8, ( B ) DLGAP5, ( C ) ORC1 and ( D ) SMC4. Transwell examination of LGG cell lines treated with siRNA or negative control (NC) to target four hub genes: ( E ) CDCA8, ( F ) DLGAP5, ( G ) ORC1 and ( H ) SMC4. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.

    Article Snippet: The HS683 human glioma cell line was sourced from Wuhan Procell Life Science and Technology Co., Ltd. (Procell, China).

    Techniques: Negative Control

    The results of CCK-8 assay in HS683 cell lines. ( A ) SMC4, ( B ) DLGAP5, CDCA8 and ( D ) ORC1. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.

    Journal: Scientific Reports

    Article Title: Stemness subtypes in lower-grade glioma with prognostic biomarkers, tumor microenvironment, and treatment response

    doi: 10.1038/s41598-024-65717-7

    Figure Lengend Snippet: The results of CCK-8 assay in HS683 cell lines. ( A ) SMC4, ( B ) DLGAP5, CDCA8 and ( D ) ORC1. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, no significance.

    Article Snippet: The HS683 human glioma cell line was sourced from Wuhan Procell Life Science and Technology Co., Ltd. (Procell, China).

    Techniques: CCK-8 Assay