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human normal hepatocytes wrl68  (ATCC)


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    Structured Review

    ATCC human normal hepatocytes wrl68
    Overexpression of SPOP could facilitate the proliferation of human normal hepatocytes <t>(WRL68).</t> (a) Transfection efficiency of SPOP in WRL68 cells was measured by qRT-PCR. (b) Proliferative abilities of WRL68 cells in the SPOP group and the vec group were detected by CCK8 assay. (c) Colony formation assay detected the proliferations of WRL68 cells in the SPOP group and the vec group. * p < 0.05, ** p < 0.01.
    Human Normal Hepatocytes Wrl68, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 40 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+normal+hepatocytes+wrl68/Wrl+68/pmc10628592-52-0-4
    Average 94 stars, based on 40 article reviews
    human normal hepatocytes wrl68 - by Bioz Stars, 2026-09
    94/100 stars

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    1) Product Images from "SPOP regulates the expression profiles and alternative splicing events in human hepatocytes"

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes

    Journal: Open Life Sciences

    doi: 10.1515/biol-2022-0755

    Overexpression of SPOP could facilitate the proliferation of human normal hepatocytes (WRL68). (a) Transfection efficiency of SPOP in WRL68 cells was measured by qRT-PCR. (b) Proliferative abilities of WRL68 cells in the SPOP group and the vec group were detected by CCK8 assay. (c) Colony formation assay detected the proliferations of WRL68 cells in the SPOP group and the vec group. * p < 0.05, ** p < 0.01.
    Figure Legend Snippet: Overexpression of SPOP could facilitate the proliferation of human normal hepatocytes (WRL68). (a) Transfection efficiency of SPOP in WRL68 cells was measured by qRT-PCR. (b) Proliferative abilities of WRL68 cells in the SPOP group and the vec group were detected by CCK8 assay. (c) Colony formation assay detected the proliferations of WRL68 cells in the SPOP group and the vec group. * p < 0.05, ** p < 0.01.

    Techniques Used: Over Expression, Transfection, Quantitative RT-PCR, CCK-8 Assay, Colony Assay

    Overexpression of SPOP could change the gene expression profiles of WRL68. (a) Boxplot of sample gene expression distribution. (b) Correlation between SPOP overexpression (SPOP rep1/2/3) and control (vec rep1/2/3) samples. (c) DEGs between the SPOP group and the vec group. (d) Correlation of log2 fold-change between RNA-Seq and RT-qPCR for significantly DEGs.
    Figure Legend Snippet: Overexpression of SPOP could change the gene expression profiles of WRL68. (a) Boxplot of sample gene expression distribution. (b) Correlation between SPOP overexpression (SPOP rep1/2/3) and control (vec rep1/2/3) samples. (c) DEGs between the SPOP group and the vec group. (d) Correlation of log2 fold-change between RNA-Seq and RT-qPCR for significantly DEGs.

    Techniques Used: Over Expression, Gene Expression, Control, RNA Sequencing, Quantitative RT-PCR

    Potential biological functions of SPOP-related genes in WRL68 cells. (a) Top 30 most enriched GO terms of the upregulated DEGs. (b) Top 30 most enriched GO terms of the downregulated DEGs. (c) Top 20 most enriched KEGG pathways of all DEGs. (d) Top 20 most enriched DisGeNET lists of all DEGs.
    Figure Legend Snippet: Potential biological functions of SPOP-related genes in WRL68 cells. (a) Top 30 most enriched GO terms of the upregulated DEGs. (b) Top 30 most enriched GO terms of the downregulated DEGs. (c) Top 20 most enriched KEGG pathways of all DEGs. (d) Top 20 most enriched DisGeNET lists of all DEGs.

    Techniques Used:

    Enrichment biological function of SPOP RASEs in WRL68 cells. (a) Number of significant RASEs. (b) GO functional enrichment of different RASEs. (c) KEGG pathway enrichment analysis results: A3SS events, 11 A5SS events, 20 MXE events, 11 RI events, and 100 SE events.
    Figure Legend Snippet: Enrichment biological function of SPOP RASEs in WRL68 cells. (a) Number of significant RASEs. (b) GO functional enrichment of different RASEs. (c) KEGG pathway enrichment analysis results: A3SS events, 11 A5SS events, 20 MXE events, 11 RI events, and 100 SE events.

    Techniques Used: Functional Assay

    HCC pathway modified by SPOP overexpression in WRL68 (the figure was drawn according to the information from KEGG PATHWAY database. The molecules in red were upregulated with SPOP overexpression and the molecules in green were downregulated with SPOP overexpression).
    Figure Legend Snippet: HCC pathway modified by SPOP overexpression in WRL68 (the figure was drawn according to the information from KEGG PATHWAY database. The molecules in red were upregulated with SPOP overexpression and the molecules in green were downregulated with SPOP overexpression).

    Techniques Used: Modification, Over Expression

    Related Articles

    Cell Culture:

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes
    Article Snippet: .. Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere. .. To establish the SPOP overexpression model, lentivirus containing the SPOP gene was constructed and packaged by GeneCopoeia (Guangzhou, China).

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes.
    Article Snippet: .. Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China)with 10%GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin– streptomycin (10,000U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO2 humidified atmosphere. .. To establish the SPOP overexpressionmodel, lentivirus containing the SPOP gene was constructed and packaged by GeneCopoeia (Guangzhou, China).

    Modification:

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes
    Article Snippet: .. Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere. .. To establish the SPOP overexpression model, lentivirus containing the SPOP gene was constructed and packaged by GeneCopoeia (Guangzhou, China).

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes.
    Article Snippet: .. Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China)with 10%GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin– streptomycin (10,000U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO2 humidified atmosphere. .. To establish the SPOP overexpressionmodel, lentivirus containing the SPOP gene was constructed and packaged by GeneCopoeia (Guangzhou, China).



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    Overexpression of SPOP could facilitate the proliferation of human normal hepatocytes <t>(WRL68).</t> (a) Transfection efficiency of SPOP in WRL68 cells was measured by qRT-PCR. (b) Proliferative abilities of WRL68 cells in the SPOP group and the vec group were detected by CCK8 assay. (c) Colony formation assay detected the proliferations of WRL68 cells in the SPOP group and the vec group. * p < 0.05, ** p < 0.01.
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    Image Search Results


    Overexpression of SPOP could facilitate the proliferation of human normal hepatocytes (WRL68). (a) Transfection efficiency of SPOP in WRL68 cells was measured by qRT-PCR. (b) Proliferative abilities of WRL68 cells in the SPOP group and the vec group were detected by CCK8 assay. (c) Colony formation assay detected the proliferations of WRL68 cells in the SPOP group and the vec group. * p < 0.05, ** p < 0.01.

    Journal: Open Life Sciences

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes

    doi: 10.1515/biol-2022-0755

    Figure Lengend Snippet: Overexpression of SPOP could facilitate the proliferation of human normal hepatocytes (WRL68). (a) Transfection efficiency of SPOP in WRL68 cells was measured by qRT-PCR. (b) Proliferative abilities of WRL68 cells in the SPOP group and the vec group were detected by CCK8 assay. (c) Colony formation assay detected the proliferations of WRL68 cells in the SPOP group and the vec group. * p < 0.05, ** p < 0.01.

    Article Snippet: Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere.

    Techniques: Over Expression, Transfection, Quantitative RT-PCR, CCK-8 Assay, Colony Assay

    Overexpression of SPOP could change the gene expression profiles of WRL68. (a) Boxplot of sample gene expression distribution. (b) Correlation between SPOP overexpression (SPOP rep1/2/3) and control (vec rep1/2/3) samples. (c) DEGs between the SPOP group and the vec group. (d) Correlation of log2 fold-change between RNA-Seq and RT-qPCR for significantly DEGs.

    Journal: Open Life Sciences

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes

    doi: 10.1515/biol-2022-0755

    Figure Lengend Snippet: Overexpression of SPOP could change the gene expression profiles of WRL68. (a) Boxplot of sample gene expression distribution. (b) Correlation between SPOP overexpression (SPOP rep1/2/3) and control (vec rep1/2/3) samples. (c) DEGs between the SPOP group and the vec group. (d) Correlation of log2 fold-change between RNA-Seq and RT-qPCR for significantly DEGs.

    Article Snippet: Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere.

    Techniques: Over Expression, Gene Expression, Control, RNA Sequencing, Quantitative RT-PCR

    Potential biological functions of SPOP-related genes in WRL68 cells. (a) Top 30 most enriched GO terms of the upregulated DEGs. (b) Top 30 most enriched GO terms of the downregulated DEGs. (c) Top 20 most enriched KEGG pathways of all DEGs. (d) Top 20 most enriched DisGeNET lists of all DEGs.

    Journal: Open Life Sciences

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes

    doi: 10.1515/biol-2022-0755

    Figure Lengend Snippet: Potential biological functions of SPOP-related genes in WRL68 cells. (a) Top 30 most enriched GO terms of the upregulated DEGs. (b) Top 30 most enriched GO terms of the downregulated DEGs. (c) Top 20 most enriched KEGG pathways of all DEGs. (d) Top 20 most enriched DisGeNET lists of all DEGs.

    Article Snippet: Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere.

    Techniques:

    Enrichment biological function of SPOP RASEs in WRL68 cells. (a) Number of significant RASEs. (b) GO functional enrichment of different RASEs. (c) KEGG pathway enrichment analysis results: A3SS events, 11 A5SS events, 20 MXE events, 11 RI events, and 100 SE events.

    Journal: Open Life Sciences

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes

    doi: 10.1515/biol-2022-0755

    Figure Lengend Snippet: Enrichment biological function of SPOP RASEs in WRL68 cells. (a) Number of significant RASEs. (b) GO functional enrichment of different RASEs. (c) KEGG pathway enrichment analysis results: A3SS events, 11 A5SS events, 20 MXE events, 11 RI events, and 100 SE events.

    Article Snippet: Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere.

    Techniques: Functional Assay

    HCC pathway modified by SPOP overexpression in WRL68 (the figure was drawn according to the information from KEGG PATHWAY database. The molecules in red were upregulated with SPOP overexpression and the molecules in green were downregulated with SPOP overexpression).

    Journal: Open Life Sciences

    Article Title: SPOP regulates the expression profiles and alternative splicing events in human hepatocytes

    doi: 10.1515/biol-2022-0755

    Figure Lengend Snippet: HCC pathway modified by SPOP overexpression in WRL68 (the figure was drawn according to the information from KEGG PATHWAY database. The molecules in red were upregulated with SPOP overexpression and the molecules in green were downregulated with SPOP overexpression).

    Article Snippet: Human normal hepatocytes WRL68 (ATCC, Manassas, USA) were cultured in Dulbecco’s Modified Eagle Medium (cat. no. PM150210, Procell, Wuhan, China) with 10% GibcoTM fetal bovine serum (cat. no. 10099141C, Invitrogen, AUS) and 1% penicillin–streptomycin (10,000 U/mL) (cat. no. 15140122, Invitrogen, USA), at 37°C in a 5% CO 2 humidified atmosphere.

    Techniques: Modification, Over Expression