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首頁 > 細(xì)胞 > 人源細(xì)胞系 > 人神經(jīng)母細(xì)胞瘤細(xì)胞(SK-N-SH)
人神經(jīng)母細(xì)胞瘤細(xì)胞(SK-N-SH)
￥800.00元
細(xì)胞貨號： CL0287
細(xì)胞種屬： 人源細(xì)胞系
細(xì)胞別名： SK N SH; SKN-SH; SK-NSH; SKNSH; NSH
發(fā)貨規(guī)格： 1×10?
供體信息： 4歲女性歐洲人
腫瘤類型： 神經(jīng)母細(xì)胞瘤
組織來源： 大腦
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背景信息
  • 種屬： 人源細(xì)胞系
  • 組織來源： 大腦
  • 腫瘤類型： 神經(jīng)母細(xì)胞瘤
  • 供體信息： 4歲女性歐洲人
  • 背景描述： 該細(xì)胞是由BiedlerJL建立的兩株神經(jīng)組織來源的細(xì)胞中的一株（另一株是SK-N-MC）。與SK-N-MC不同，該細(xì)胞倍增時(shí)間更長，表達(dá)更高水平的多巴胺-β-羥化酶；常作為細(xì)胞介導(dǎo)的細(xì)胞毒性分析的靶細(xì)胞。
培養(yǎng)建議
  • 生長形態(tài)： 上皮細(xì)胞樣
  • 生長特性： 貼壁
  • 培養(yǎng)條件： MEM+10%FBS+1%P/S
  • 凍存條件： 90%FBS+10%DMSO
  • 血清使用等級： 標(biāo)準(zhǔn)
  • 傳代方式： 胰酶消化
  • 倍增時(shí)間： 44h
  • 傳代比例： 胰酶消化
  • 換液頻率： 每周2~3次
  • 生物安全等級： 1
  • 培養(yǎng)注意事項(xiàng)：
其他信息
  • 蛋白表達(dá)： Plasminogen Activator, Shows Increased Expression Of M-Csf After Treatment With Amyloid-Beta Peptide.
  • 同工酶： AK-1, 1；ES-D, 1；G6PD, B；GLO-I, 1；Me-2, 2；PGM1, 1；PGM3, 1
  • 基因表達(dá)： plasminogen activator; increased expression of M-CSF after treatment with amyloid-beta peptide.
  • 抗原表達(dá)： Blood Type A; Rh+
  • 核型： The cell line is hyperdiploid human female (XX), with the modal chromosome number of 47. Normal chromosomes N9 and N22 are single. One copy of each of these chromosomes is structurally altered to form the two marker chromosomes 9q+ and 22q+., Chromosomes N7 is trisomic. Extra bands were found on one copy of chromosome N7, thereby forming a marker chromosome as described by R.C. Seeger. May have been translocated in part(s) to the q arms of chromosomes N9 and N22.
人神經(jīng)母細(xì)胞瘤細(xì)胞
Catalog No CL0287
Product information
  • 蛋白表達(dá)： Plasminogen Activator, Shows Increased Expression Of M-Csf After Treatment With Amyloid-Beta Peptide.
  • 同工酶： AK-1, 1；ES-D, 1；G6PD, B；GLO-I, 1；Me-2, 2；PGM1, 1；PGM3, 1
  • 基因表達(dá)： plasminogen activator; increased expression of M-CSF after treatment with amyloid-beta peptide.
  • 抗原表達(dá)： Blood Type A; Rh+
  • 核型： The cell line is hyperdiploid human female (XX), with the modal chromosome number of 47. Normal chromosomes N9 and N22 are single. One copy of each of these chromosomes is structurally altered to form the two marker chromosomes 9q+ and 22q+., Chromosomes N7 is trisomic. Extra bands were found on one copy of chromosome N7, thereby forming a marker chromosome as described by R.C. Seeger. May have been translocated in part(s) to the q arms of chromosomes N9 and N22.
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