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transwell chambers corning  (Corning Life Sciences)

 
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    Corning Life Sciences transwell chambers corning
    Transwell Chambers Corning, supplied by Corning Life Sciences, 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/transwell chambers corning/product/Corning Life Sciences
    Average 90 stars, based on 1 article reviews
    transwell chambers corning - by Bioz Stars, 2026-02
    90/100 stars

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    Functional analysis of SNRPB knockdown in HCC cells. ( A ) Validation of SNRPB knockdown efficiency in SK-HEP-1 and HCCLM3 cells at both mRNA and protein levels using two effective shRNAs (shSNRPB-2 and shSNRPB-3). ( B ) CCK-8 assay demonstrates the inhibitory effects of SNRPB knockdown on HCC cell proliferation in SK-HEP-1 and HCCLM3 cells. ( C ) Colony formation assay shows that SNRPB knockdown significantly suppresses the clonogenic capacity of HCC cells. ( D ) Flow cytometry analysis reveals that SNRPB knockdown significantly increases apoptosis rates in SK-HEP-1 and HCCLM3 cells. ( E ) <t>Transwell</t> assay demonstrates that silencing SNRPB significantly reduces the migratory capacity of HCC cells. ( F ) The pictures taken from the excised xenografts of indicated experimental groups. ( G ) Tumor volume measurements in subcutaneous xenograft tumor models showing the effects of SNRPB knockdown on tumor growth. ( H ) Tumor weight analysis at the time of sacrifice in xenograft models. ( I ) IHC staining of tumor tissues showing Ki67 expression levels. Data were drawn as mean ± SD ( n ≥ 3). * P < 0.05, ** P < 0.01, *** P < 0.001
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    Average 90 stars, based on 1 article reviews
    transwell chamber corning - by Bioz Stars, 2026-02
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    transwell chambers in the presence of matrigel corning 354,480  (Corning Life Sciences)
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    Functional analysis of SNRPB knockdown in HCC cells. ( A ) Validation of SNRPB knockdown efficiency in SK-HEP-1 and HCCLM3 cells at both mRNA and protein levels using two effective shRNAs (shSNRPB-2 and shSNRPB-3). ( B ) CCK-8 assay demonstrates the inhibitory effects of SNRPB knockdown on HCC cell proliferation in SK-HEP-1 and HCCLM3 cells. ( C ) Colony formation assay shows that SNRPB knockdown significantly suppresses the clonogenic capacity of HCC cells. ( D ) Flow cytometry analysis reveals that SNRPB knockdown significantly increases apoptosis rates in SK-HEP-1 and HCCLM3 cells. ( E ) <t>Transwell</t> assay demonstrates that silencing SNRPB significantly reduces the migratory capacity of HCC cells. ( F ) The pictures taken from the excised xenografts of indicated experimental groups. ( G ) Tumor volume measurements in subcutaneous xenograft tumor models showing the effects of SNRPB knockdown on tumor growth. ( H ) Tumor weight analysis at the time of sacrifice in xenograft models. ( I ) IHC staining of tumor tissues showing Ki67 expression levels. Data were drawn as mean ± SD ( n ≥ 3). * P < 0.05, ** P < 0.01, *** P < 0.001
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    Functional analysis of SNRPB knockdown in HCC cells. ( A ) Validation of SNRPB knockdown efficiency in SK-HEP-1 and HCCLM3 cells at both mRNA and protein levels using two effective shRNAs (shSNRPB-2 and shSNRPB-3). ( B ) CCK-8 assay demonstrates the inhibitory effects of SNRPB knockdown on HCC cell proliferation in SK-HEP-1 and HCCLM3 cells. ( C ) Colony formation assay shows that SNRPB knockdown significantly suppresses the clonogenic capacity of HCC cells. ( D ) Flow cytometry analysis reveals that SNRPB knockdown significantly increases apoptosis rates in SK-HEP-1 and HCCLM3 cells. ( E ) Transwell assay demonstrates that silencing SNRPB significantly reduces the migratory capacity of HCC cells. ( F ) The pictures taken from the excised xenografts of indicated experimental groups. ( G ) Tumor volume measurements in subcutaneous xenograft tumor models showing the effects of SNRPB knockdown on tumor growth. ( H ) Tumor weight analysis at the time of sacrifice in xenograft models. ( I ) IHC staining of tumor tissues showing Ki67 expression levels. Data were drawn as mean ± SD ( n ≥ 3). * P < 0.05, ** P < 0.01, *** P < 0.001

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: SNRPB/CCNB1 axis promotes hepatocellular carcinoma progression and cisplatin resistance through enhancing lipid metabolism reprogramming

    doi: 10.1186/s13046-025-03463-y

    Figure Lengend Snippet: Functional analysis of SNRPB knockdown in HCC cells. ( A ) Validation of SNRPB knockdown efficiency in SK-HEP-1 and HCCLM3 cells at both mRNA and protein levels using two effective shRNAs (shSNRPB-2 and shSNRPB-3). ( B ) CCK-8 assay demonstrates the inhibitory effects of SNRPB knockdown on HCC cell proliferation in SK-HEP-1 and HCCLM3 cells. ( C ) Colony formation assay shows that SNRPB knockdown significantly suppresses the clonogenic capacity of HCC cells. ( D ) Flow cytometry analysis reveals that SNRPB knockdown significantly increases apoptosis rates in SK-HEP-1 and HCCLM3 cells. ( E ) Transwell assay demonstrates that silencing SNRPB significantly reduces the migratory capacity of HCC cells. ( F ) The pictures taken from the excised xenografts of indicated experimental groups. ( G ) Tumor volume measurements in subcutaneous xenograft tumor models showing the effects of SNRPB knockdown on tumor growth. ( H ) Tumor weight analysis at the time of sacrifice in xenograft models. ( I ) IHC staining of tumor tissues showing Ki67 expression levels. Data were drawn as mean ± SD ( n ≥ 3). * P < 0.05, ** P < 0.01, *** P < 0.001

    Article Snippet: The assessment of cell migration was conducted using a Transwell chamber (Corning).

    Techniques: Functional Assay, Knockdown, Biomarker Discovery, CCK-8 Assay, Colony Assay, Flow Cytometry, Transwell Assay, Immunohistochemistry, Expressing