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人肝癌细胞SK-HEP-1

人肝癌细胞SK-HEP-1

简要描述:青旗(上海)生物技术发展有限公司所提供的人肝癌细胞SK-HEP-1质量可靠、规格齐全,青旗(上海)生物技术发展有限公司不仅具有专业的技术水平,更有良好的售后服务和优质的解决方案,欢迎您来电咨询此产品具体参数及价格等详细信息!

更新时间:2022-12-11

厂商性质:生产厂家

浏览次数:

详情介绍
品牌自营品牌货号BFN60800688
规格T25培养瓶x1 1.5ml冻存管x2供货周期现货
主要用途仅供科研应用领域医疗卫生,生物产业

细胞名称

人肝癌细SK-HEP-1

img1

货物编码

BFN60800688

产品规格

T25培养x1

1.5ml冻存x2

细胞数量

1x10^6

1x10^6

保存温度

37

-198

运输方式

常温保温运输

干冰运输

安全等级

1

用途限制

仅供科研用途

培养体系

DMEM高糖培养基Hyclone+10%胎牛血清Gibco+1%双抗Hyclone

培养温度

37

二氧化碳浓度

5%

简介

人肝癌细胞SK-HEP-1细胞已被鉴定为内皮来源。该细胞系为异倍体女性人XX),染色体在亚三倍体范围内。在裸鼠中,它能形成与肝癌相一致的大细胞癌。人肝癌细胞SK-HEP-1细胞由青旗(上海)生物技术发展有限公司2017年引种ATCC(HTB-52)

注释

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

AmelogeninX,XCSF1PO11,12D12S39118,18D13S3178,12D16S53912,12D18S5113,15D19S43312,15.2D21S1129,31D2S133820,23D3S135816,16D5S81810,13D6S104311,11D7S8208,11D8S117913,14FGA17,17PentaE13,21TH017,9TPOX9,9vWA14,17

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验收细胞注意事

1、收到人肝癌细SK-HEP-1细胞,请查看瓶子是否有破裂,培养基是否漏出,是否浑浊,如有请尽快联系

2、收到人肝癌细SK-HEP-1细胞,如包装完好,请在显微镜下观察细胞,由于运输过程中的问题,细胞培养瓶中的贴壁细胞有可能从瓶壁中脱落下来,显微镜下观察会出现细胞悬浮的情况,出现此状态时,请不要打开细胞培养瓶,应立即将培养瓶置于细胞培养箱里静 3-5 小时左右,让细胞先稳定下,再于显微镜下观察,此时多数细胞会重新贴附于瓶壁。如细胞仍不能贴壁,请用台盼蓝染色法鉴定细胞活力,如台盼蓝染色证实细胞活力正常请按悬浮细胞的方法处理

3、收到人肝癌细SK-HEP-1细胞后,请镜下观察细胞,用恰当方式处理细胞。若悬浮的细胞较多,请离心收集细胞,接种到一个新的培养瓶中。弃掉原液,使用新鲜配制的培养基,使用进口胎牛血清。刚接到细胞,若细胞不多 血清浓度可以加 15%去培养。若细胞迏 80% ,血清浓度还是 10

4、收到人肝癌细SK-HEP-1细胞时如无异常情 ,请在显微镜下观察细胞密度,如为贴壁细胞,未超80%汇合度时,将培养瓶中培养基吸出,留 5-10ML 培养基继续培养:超 80%汇合度时,请按细胞培养条件传代培养。如为悬浮细胞,吸出培养液1000 /分钟离 3 分钟,吸出上清,管底细胞用新鲜培养基悬浮细胞后移回培养瓶

5、将培养瓶置 37培养箱中培养,盖子微微拧松。吸出的培养基可以保存在灭菌过的瓶子里,存放 4冰箱,以备不时之需

624 小时后,人肝癌细SK-HEP-1细胞形态已恢复并贴满瓶壁,即可传代。(贴壁细胞)将培养瓶里的培养基倒去, 3-5ml(以能覆盖细胞生长面为准PBS Hanks液洗涤后弃去。 0.5-1ml 0.25% EDTA 的胰酶消化,消化时间以具体细胞为准,一 1-3 分钟,不超 5 分钟。可以放37培养箱消化。轻轻晃动瓶壁,见细胞脱落下来,加 3-5ml 培养基终止消化。用移液管轻轻吹打瓶壁上的细胞,使之*脱落,然后将溶液吸入离心管内离心1000rpm/5min。弃上清,视细胞数量决定分瓶数,一般一传二,如细胞量多可一传三,有些细胞不易传得过稀,有些生长较快的细胞则可以多传几瓶,以具体细胞和经验为准。(悬浮细胞)用移液管轻轻吹打瓶壁,直接将溶液吸入离心管离心即可

7、贴壁细 ,悬浮细胞。严格无菌操作。换液时,换新的细胞培养瓶和换新鲜的培养液375%CO2 培养。

特别提醒 原瓶中培养基不宜继续使用,请更换新鲜培养基培养。




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