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簡(jiǎn)要描述:青旗(上海)生物技術(shù)發(fā)展有限公司,總部位于上海浦東新區(qū),依托本地高校資源,逐步發(fā)展成為以生物技術(shù)為主的研發(fā)、生產(chǎn)、培訓(xùn)為一體的綜合化產(chǎn)業(yè)平臺(tái),在標(biāo)準(zhǔn)化細(xì)胞庫(kù)建立及細(xì)胞藥物前端模型方面成果顯著。公司生產(chǎn)經(jīng)營(yíng)原代細(xì)胞、細(xì)胞系、ELISA試劑盒、感受態(tài)細(xì)胞和HPLC檢測(cè)等科研產(chǎn)品與服務(wù)。我們秉承對(duì)用戶負(fù)責(zé)的態(tài)度,以對(duì)科研的高度嚴(yán)謹(jǐn),以嚴(yán)格的質(zhì)量控制,為廣大生物醫(yī)學(xué)科研用戶提供更優(yōu)質(zhì)的服務(wù)!
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品牌 | 其他品牌 | 貨號(hào) | BFN60800692 |
---|---|---|---|
規(guī)格 | T25培養(yǎng)瓶x1 1.5ml凍存管x2 | 供貨周期 | 現(xiàn)貨 |
主要用途 | 僅供科研 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,生物產(chǎn)業(yè) |
細(xì)胞名稱 | 人肝癌細(xì)胞HepG2 | ||
貨物編碼 | BFN60800692 | ||
產(chǎn)品規(guī)格 | T25培養(yǎng)瓶x1 | 1.5ml凍存管x2 | |
細(xì)胞數(shù)量 | 1x10^6 | 1x10^6 | |
保存溫度 | 37℃ | -198℃ | |
運(yùn)輸方式 | 常溫保溫運(yùn)輸 | 干冰運(yùn)輸 | |
安全等級(jí) | 1 | ||
用途限制 | 僅供科研用途 1類 |
培養(yǎng)體系 | DMEM高糖培養(yǎng)基(Hyclone)+10%胎牛血清(Gibco)+1%雙抗(Hyclone) | ||
培養(yǎng)溫度 | 37℃ | 二氧化碳濃度 | 5% |
簡(jiǎn)介 | 人肝癌細(xì)胞HepG2細(xì)胞來(lái)源于一名15歲的白人少年的肝癌組織。該細(xì)胞表達(dá)甲胎蛋白、白蛋白、α-2-巨球蛋白、α-1-抗胰蛋白酶、轉(zhuǎn)鐵蛋白、α-1-抗凝乳蛋白酶、結(jié)合珠蛋白、銅藍(lán)蛋白、纖溶酶原、補(bǔ)體C4、C3激活物、纖維蛋白原、α-1酸性糖蛋白、α-2-HS-糖蛋白、β-脂蛋白、視黃醇結(jié)合蛋白;表達(dá)胰島素受體和胰島素樣生長(zhǎng)因子IGFⅡ的受體;該細(xì)胞具有3-羥基-3-甲酰輔酶A還原酶和肝甘油三酯脂肪酶的活性。目前尚未證明該細(xì)胞中有HBV基因組。 人肝癌細(xì)胞HepG2細(xì)胞由青旗(上海)生物技術(shù)發(fā)展有限公司于2019年引種自ATCC(HB-8065)。 | ||
注釋 | Problematic cell line: Misidentified. Originally thought to be a hepatocellular carcinoma cell line but shown to be from an hepatoblastoma (PubMed=19751877). Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: ENCODE project common cell types; tier 1. Part of: JFCR45 cancer cell line panel. Part of: MD Anderson Cell Lines Project. Part of: TCGA-110-CL cell line panel. Doubling time: ~50-60 hours (DSMZ). Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep phosphoproteome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Genome sequenced. Omics: H3K27ac ChIP-seq epigenome analysis. Omics: H3K27me3 ChIP-seq epigenome analysis. Omics: H3K36me3 ChIP-seq epigenome analysis. Omics: H3K4me1 ChIP-seq epigenome analysis. Omics: H3K4me2 ChIP-seq epigenome analysis. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: H3K79me2 ChIP-seq epigenome analysis. Omics: H3K9ac ChIP-seq epigenome analysis. Omics: H3K9me3 ChIP-seq epigenome analysis. Omics: H4K20me1 ChIP-seq epigenome analysis. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: Secretome proteome analysis. Omics: SNP array analysis. Omics: Transcriptome analysis. Omics: Virome analysis using proteomics. | ||
STR信息 | Amelogenin:X,Y;CSF1PO:10,11;D13S317:9,13;D16S539:12,13;D18S51:13,14;D19S433:15.2;D21S11:29,31;D2S1338:19,20;D3S1358:15,16;D5S818:11,12;D7S820:10;D8S1179:15,16;FGA:22,25;TH01:9;TPOX:8,9;vWA:17; | ||
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驗(yàn)收細(xì)胞注意事項(xiàng)
1、收到人肝癌細(xì)胞HepG2細(xì)胞,請(qǐng)查看瓶子是否有破裂,培養(yǎng)基是否漏出,是否渾濁,如有請(qǐng)盡快聯(lián)系。
2、收到人肝癌細(xì)胞HepG2細(xì)胞,如包裝完好,請(qǐng)?jiān)陲@微鏡下觀察細(xì)胞。,由于運(yùn)輸過(guò)程中的問(wèn)題,細(xì)胞培養(yǎng)瓶中的貼壁細(xì)胞有可能從瓶壁中脫落下來(lái),顯微鏡下觀察會(huì)出現(xiàn)細(xì)胞懸浮的情況,出現(xiàn)此狀態(tài)時(shí),請(qǐng)不要打開(kāi)細(xì)胞培養(yǎng)瓶,應(yīng)立即將培養(yǎng)瓶置于細(xì)胞培養(yǎng)箱里靜止 3-5 小時(shí)左右,讓細(xì)胞先穩(wěn)定下,再于顯微鏡下觀察,此時(shí)多數(shù)細(xì)胞會(huì)重新貼附于瓶壁。如細(xì)胞仍不能貼壁,請(qǐng)用臺(tái)盼藍(lán)染色法鑒定細(xì)胞活力,如臺(tái)盼藍(lán)染色證實(shí)細(xì)胞活力正常請(qǐng)按懸浮細(xì)胞的方法處理。
3、收到人肝癌細(xì)胞HepG2細(xì)胞后,請(qǐng)鏡下觀察細(xì)胞,用恰當(dāng)方式處理細(xì)胞。若懸浮的細(xì)胞較多,請(qǐng)離心收集細(xì)胞,接種到一個(gè)新的培養(yǎng)瓶中。棄掉原液,使用新鮮配制的培養(yǎng)基,使用進(jìn)口胎牛血清。剛接到細(xì)胞,若細(xì)胞不多時(shí) 血清濃度可以加到 15%去培養(yǎng)。若細(xì)胞迏到 80%左右 ,血清濃度還是在 10%。
4、收到人肝癌細(xì)胞HepG2細(xì)胞時(shí)如無(wú)異常情況 ,請(qǐng)?jiān)陲@微鏡下觀察細(xì)胞密度,如為貼壁細(xì)胞,未超過(guò)80%匯合度時(shí),將培養(yǎng)瓶中培養(yǎng)基吸出,留下 5-10ML 培養(yǎng)基繼續(xù)培養(yǎng):超過(guò) 80%匯合度時(shí),請(qǐng)按細(xì)胞培養(yǎng)條件傳代培養(yǎng)。如為懸浮細(xì)胞,吸出培養(yǎng)液,1000 轉(zhuǎn)/分鐘離心 3 分鐘,吸出上清,管底細(xì)胞用新鮮培養(yǎng)基懸浮細(xì)胞后移回培養(yǎng)瓶。
5、將培養(yǎng)瓶置于 37℃培養(yǎng)箱中培養(yǎng),蓋子微微擰松。吸出的培養(yǎng)基可以保存在滅菌過(guò)的瓶子里,存放于 4℃冰箱,以備不時(shí)之需。
6、24 小時(shí)后,人肝癌細(xì)胞HepG2細(xì)胞形態(tài)已恢復(fù)并貼滿瓶壁,即可傳代。(貼壁細(xì)胞)將培養(yǎng)瓶里的培養(yǎng)基倒去,加 3-5ml(以能覆蓋細(xì)胞生長(zhǎng)面為準(zhǔn))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(shí)間以具體細(xì)胞為準(zhǔn),一般 1-3 分鐘,不超過(guò) 5 分鐘。可以放入37℃培養(yǎng)箱消化。輕輕晃動(dòng)瓶壁,見(jiàn)細(xì)胞脫落下來(lái),加入 3-5ml 培養(yǎng)基終止消化。用移液管輕輕吹打瓶壁上的細(xì)胞,使之*脫落,然后將溶液吸入離心管內(nèi)離心,1000rpm/5min。棄上清,視細(xì)胞數(shù)量決定分瓶數(shù),一般一傳二,如細(xì)胞量多可一傳三,有些細(xì)胞不易傳得過(guò)稀,有些生長(zhǎng)較快的細(xì)胞則可以多傳幾瓶,以具體細(xì)胞和經(jīng)驗(yàn)為準(zhǔn)。(懸浮細(xì)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(xì)胞 ,懸浮細(xì)胞。嚴(yán)格無(wú)菌操作。換液時(shí),換新的細(xì)胞培養(yǎng)瓶和換新鮮的培養(yǎng)液,37℃,5%CO2 培養(yǎng)。
特別提醒: 原瓶中培養(yǎng)基不宜繼續(xù)使用,請(qǐng)更換新鮮培養(yǎng)基培養(yǎng)。