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human nb cell lines sk n sh sk  (ATCC)


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    ATCC human nb cell lines sk n sh sk
    Human Nb Cell Lines Sk N Sh Sk, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1703 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sk+n+sh+human+nb+cell+lines/SK-N-SH/us12636386-378-2-22
    Average 96 stars, based on 1703 article reviews
    human nb cell lines sk n sh sk - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Quantitative RT-PCR:

    Article Title: RT-qPCR for PHOX2B mRNA is a highly specific and sensitive method to assess neuroblastoma minimal residual disease in testicular tissue
    Article Snippet: .. The specificity and sensitivity of NB MRD detection were assessed by RT-qPCR quantification of TH , PHOX2B and DCX mRNA expression in thawed testicular tissues that were contaminated with IMR-32 and SK-N-SH human NB cell lines (CCL-127 and HTB-11; American Type Culture Collection, Manassas, VA, USA). ..

    Expressing:

    Article Title: RT-qPCR for PHOX2B mRNA is a highly specific and sensitive method to assess neuroblastoma minimal residual disease in testicular tissue
    Article Snippet: .. The specificity and sensitivity of NB MRD detection were assessed by RT-qPCR quantification of TH , PHOX2B and DCX mRNA expression in thawed testicular tissues that were contaminated with IMR-32 and SK-N-SH human NB cell lines (CCL-127 and HTB-11; American Type Culture Collection, Manassas, VA, USA). ..



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    FKA treatment suppresses the proliferative and clone-forming abilities of NB cells. A The structure of FKA. B HUVECs were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of HUVECs was detected by CCK-8 assay. C <t>Human</t> NB <t>cell</t> <t>line</t> (SK-N-SH) was treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of SK-N-SH cells was detected by CCK-8 assay. D SK-N-SH cells were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The clone-forming ability of SK-N-SH cells was detected by colony formation assay. *** p < 0.001
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    FKA treatment suppresses the proliferative and clone-forming abilities of NB cells. A The structure of FKA. B HUVECs were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of HUVECs was detected by CCK-8 assay. C <t>Human</t> NB <t>cell</t> <t>line</t> (SK-N-SH) was treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of SK-N-SH cells was detected by CCK-8 assay. D SK-N-SH cells were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The clone-forming ability of SK-N-SH cells was detected by colony formation assay. *** p < 0.001
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    FKA treatment suppresses the proliferative and clone-forming abilities of NB cells. A The structure of FKA. B HUVECs were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of HUVECs was detected by CCK-8 assay. C Human NB cell line (SK-N-SH) was treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of SK-N-SH cells was detected by CCK-8 assay. D SK-N-SH cells were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The clone-forming ability of SK-N-SH cells was detected by colony formation assay. *** p < 0.001

    Journal: Discover Oncology

    Article Title: Flavokawain A suppresses the malignant progression of neuroblastoma in vitro depending on inactivation of ERK/VEGF/MMPs signaling pathway

    doi: 10.1007/s12672-024-01568-y

    Figure Lengend Snippet: FKA treatment suppresses the proliferative and clone-forming abilities of NB cells. A The structure of FKA. B HUVECs were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of HUVECs was detected by CCK-8 assay. C Human NB cell line (SK-N-SH) was treated with 0, 12.5, 25, 50 μM FKA for 48 h. The viability of SK-N-SH cells was detected by CCK-8 assay. D SK-N-SH cells were treated with 0, 12.5, 25, 50 μM FKA for 48 h. The clone-forming ability of SK-N-SH cells was detected by colony formation assay. *** p < 0.001

    Article Snippet: Human NB cell line (SK-N-SH) and human umbilical vein endothelial cells (HUVECs) purchased from iCell Bioscience (Shanghai, China) were cultured in DMEM (Gibco, CA, USA) supplemented with 10% FBS and 1% penicillin–streptomycin at 37 °C in a humidified incubator containing 5% CO 2 .

    Techniques: CCK-8 Assay, Colony Assay