| 品牌 | 其他品牌 | 貨號 | BFN60800688 |
|---|---|---|---|
| 規格 | T25培養瓶x1 1.5ml凍存管x2 | 供貨周期 | 現貨 |
| 主要用途 | 僅供科研 | 應用領域 | 醫療衛生,生物產業 |
細胞名稱 | 人肝癌細胞SK-HEP-1 |
| |
貨物編碼 | BFN60800688 | ||
產品規格 | T25培養瓶x1 | 1.5ml凍存管x2 | |
細胞數量 | 1x10^6 | 1x10^6 | |
保存溫度 | 37℃ | -198℃ | |
運輸方式 | 常溫保溫運輸 | 干冰運輸 | |
安全等級 | 1 | ||
用途限制 | 僅供科研用途 | ||
培養體系 | DMEM高糖培養基（Hyclone）+10%胎牛血清（Gibco）+1%雙抗（Hyclone） | ||
培養溫度 | 37℃ | 二氧化碳濃度 | 5% |
簡介 | 人肝癌細胞SK-HEP-1細胞已被鑒定為內皮來源。該細胞系為異倍體女性人（XX），染色體在亞三倍體范圍內。在裸鼠中，它能形成與肝癌相一致的大細胞癌。人肝癌細胞SK-HEP-1細胞由青旗（上海）生物技術發展有限公司于2017年引種自ATCC(HTB-52)。 | ||
注釋 | Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Part of: MD Anderson Cell Lines Project. From: Memorial Sloan Kettering Cancer Center; New York; USA. Registration: Memorial Sloan Kettering Cancer Center Office of Technology Development; SK1980-535. Characteristics: Has lost chromosome Y. Doubling time: 46.7 +- 10.3 hours, 94.2 hours (in CDM4-CHO medium), 289.8 hours (in 293 SFM II medium) (PubMed=25822314); ~30 hours (DSMZ). Microsatellite instability: Stable (MSS) (Sanger). Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: Secretome proteome analysis. Omics: SNP array analysis. Omics: Transcriptome analysis. | ||
STR信息 | Amelogenin：X,X；CSF1PO：11,12；D12S391：18,18；D13S317：8,12；D16S539：12,12；D18S51：13,15；D19S433：12,15.2；D21S11：29,31；D2S1338：20,23；D3S1358：16,16；D5S818：10,13；D6S1043：11,11；D7S820：8,11；D8S1179：13,14；FGA：17,17；PentaE：13,21；TH01：7,9；TPOX：9,9；vWA：14,17； | ||
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驗收細胞注意事項
1、收到人肝癌細胞SK-HEP-1細胞，請查看瓶子是否有破裂，培養基是否漏出，是否渾濁，如有請盡快聯系。
2、收到人肝癌細胞SK-HEP-1細胞，如包裝完好，請在顯微鏡下觀察細胞。,由于運輸過程中的問題，細胞培養瓶中的貼壁細胞有可能從瓶壁中脫落下來，顯微鏡下觀察會出現細胞懸浮的情況，出現此狀態時，請不要打開細胞培養瓶，應立即將培養瓶置于細胞培養箱里靜止 3-5 小時左右，讓細胞先穩定下，再于顯微鏡下觀察，此時多數細胞會重新貼附于瓶壁。如細胞仍不能貼壁，請用臺盼藍染色法鑒定細胞活力，如臺盼藍染色證實細胞活力正常請按懸浮細胞的方法處理。
3、收到人肝癌細胞SK-HEP-1細胞后，請鏡下觀察細胞，用恰當方式處理細胞。若懸浮的細胞較多，請離心收集細胞，接種到一個新的培養瓶中。棄掉原液，使用新鮮配制的培養基，使用進口胎牛血清。剛接到細胞，若細胞不多時 血清濃度可以加到 15％去培養。若細胞迏到 80%左右 ，血清濃度還是在 10％。
4、收到人肝癌細胞SK-HEP-1細胞時如無異常情況 ，請在顯微鏡下觀察細胞密度，如為貼壁細胞，未超過80%匯合度時，將培養瓶中培養基吸出，留下 5-10ML 培養基繼續培養：超過 80%匯合度時，請按細胞培養條件傳代培養。如為懸浮細胞，吸出培養液，1000 轉/分鐘離心 3 分鐘，吸出上清，管底細胞用新鮮培養基懸浮細胞后移回培養瓶。
5、將培養瓶置于 37℃培養箱中培養，蓋子微微擰松。吸出的培養基可以保存在滅菌過的瓶子里，存放于 4℃冰箱，以備不時之需。
6、24 小時后，人肝癌細胞SK-HEP-1細胞形態已恢復并貼滿瓶壁，即可傳代。（貼壁細胞）將培養瓶里的培養基倒去，加 3-5ml（以能覆蓋細胞生長面為準）PBS 或 Hanks’液洗滌后棄去。加 0.5-1ml 0.25%含 EDTA 的胰酶消化，消化時間以具體細胞為準，一般 1-3 分鐘，不超過 5 分鐘。可以放入37℃培養箱消化。輕輕晃動瓶壁，見細胞脫落下來，加入 3-5ml 培養基終止消化。用移液管輕輕吹打瓶壁上的細胞，使之*脫落，然后將溶液吸入離心管內離心，1000rpm/5min。棄上清，視細胞數量決定分瓶數，一般一傳二，如細胞量多可一傳三，有些細胞不易傳得過稀，有些生長較快的細胞則可以多傳幾瓶，以具體細胞和經驗為準。（懸浮細胞）用移液管輕輕吹打瓶壁，直接將溶液吸入離心管離心即可。
7、貼壁細胞 ，懸浮細胞。嚴格無菌操作。換液時，換新的細胞培養瓶和換新鮮的培養液，37℃，5%CO2 培養。
特別提醒： 原瓶中培養基不宜繼續使用，請更換新鮮培養基培養。
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