產(chǎn)品展示
虹膜色素上皮細(xì)胞總DNA
點(diǎn)擊次數(shù):12發(fā)布時(shí)間:2016/7/22 14:11:24

更新日期:2016/7/22 14:11:24
所 在 地:中國(guó)大陸
產(chǎn)品型號(hào):
優(yōu)質(zhì)供應(yīng)
詳細(xì)內(nèi)容
【虹膜色素上皮細(xì)胞總DNA】下面是細(xì)胞株培養(yǎng)的具體無(wú)菌技術(shù)要點(diǎn):
1. 實(shí)驗(yàn)開始前,無(wú)菌室和無(wú)菌操作臺(tái)需要紫外光照射30到60分鐘完全滅菌,用70%ethanol擦拭無(wú)菌操作臺(tái)面,并且打開無(wú)菌操作臺(tái)風(fēng)扇運(yùn)行10分鐘之后,才可以進(jìn)行實(shí)驗(yàn)操作。每次操作只能處理一株細(xì)胞株,即使培養(yǎng)基完全相同也不可共用培養(yǎng)基,以避免細(xì)胞間污染或失誤混淆。實(shí)驗(yàn)完成后,請(qǐng)將實(shí)驗(yàn)物品拿出工作臺(tái),用70%ethanol再次擦拭無(wú)菌操作臺(tái)面。操作間隔應(yīng)該讓無(wú)菌操作臺(tái)運(yùn)轉(zhuǎn)10分鐘到15分鐘后,才能進(jìn)行下一個(gè)細(xì)胞株的操作。
2. 無(wú)菌操作工作的區(qū)域應(yīng)保持清潔和寬敞,必要物品(試管架、吸管、吸取器或吸管盒等)可以暫時(shí)放置,其它實(shí)驗(yàn)用品使用完畢后應(yīng)移出,有利于空氣流通。實(shí)驗(yàn)用品需70%ethanol擦拭后方可帶入無(wú)菌操作臺(tái)內(nèi)。實(shí)驗(yàn)操作過(guò)程應(yīng)在臺(tái)面的中央無(wú)菌區(qū)域內(nèi)完成,請(qǐng)勿在邊緣非無(wú)菌區(qū)域進(jìn)行操作。
3. 小心取用無(wú)菌實(shí)驗(yàn)物品,避免細(xì)菌污染。請(qǐng)勿觸碰吸管尖頭部和容器瓶口處,也不要在打開的容器正上方進(jìn)行操作。容器打開后,請(qǐng)用手夾住瓶蓋并輕握瓶身,傾斜大約45°角取用,盡量不要將瓶蓋口朝上放置于桌面。
4. 工作人員應(yīng)當(dāng)首先注意自身安全,必須穿戴齊實(shí)驗(yàn)衣和實(shí)驗(yàn)手套后才能進(jìn)行實(shí)驗(yàn)。對(duì)于病毒感染或是來(lái)自人類的細(xì)胞株應(yīng)當(dāng)特別小心操作,并選擇適當(dāng)?shù)燃?jí)的無(wú)菌操作臺(tái)進(jìn)行(至少是Class II)。操作過(guò)程中,應(yīng)避免引起aerosol的產(chǎn)生,小心有毒性藥品,例如DMSO和TPA等,并避免針頭的傷害等等。
5. 定期檢測(cè)下列項(xiàng)目:
5.1. CO2鋼瓶的CO2壓力
5.2. CO2培養(yǎng)箱的CO2濃度、溫度、和水盤是否有污染(水盤的水需用無(wú)菌水,每周定時(shí)更換)。
5.3. 無(wú)菌操作臺(tái)內(nèi)的airflow壓力,定期更換紫外線燈管和HEPA過(guò)濾膜,預(yù)濾網(wǎng)(300小時(shí)/預(yù)濾網(wǎng),3000小時(shí)/HEPA)。
6. 水槽內(nèi)可添加消毒劑(Zephrin 1:750),需定期更換水槽中的水。
【虹膜色素上皮細(xì)胞總DNA】齊一生物友情提醒,本產(chǎn)品僅供科研使用,不得用于臨床及診斷使用!
一細(xì)胞說(shuō)明,具體詳細(xì)請(qǐng)見(jiàn)細(xì)胞附帶說(shuō)明書
二、客戶自備試劑
1、PBS
2、 2、RPMI-1640 培養(yǎng)基(不含 Hepes)+ 10%胎牛血清+ 1%雙抗
3、0.25% (W/V)胰蛋白酶(含 0.02% EDTA)
三、細(xì)胞背景
1、生長(zhǎng)方式:貼壁
2、種屬:Homo sapiens 人
四、培養(yǎng)條件
1、培養(yǎng)基:RPMI-1640 培養(yǎng)基(不含 Hepes)+ 10%胎牛血清+ 1%雙抗
2、溫度:37.0°C
3、氣體:空氣 95%,CO2 5%
【虹膜色素上皮細(xì)胞總DNA】五、培養(yǎng)方法
收到細(xì)胞后,在倒置顯微鏡下觀察整個(gè)細(xì)胞生長(zhǎng)情況:
如果細(xì)胞未長(zhǎng)滿,用 75%酒精噴灑整個(gè)瓶消毒后放到超菌臺(tái)內(nèi),嚴(yán)格無(wú)菌操作,打開細(xì)胞培養(yǎng)瓶,留10ml 培養(yǎng)液繼續(xù)培養(yǎng)。如果細(xì)胞已長(zhǎng)滿(達(dá) 80-90%)。即可進(jìn)行傳代,具六、體步驟如下:
1,棄去培養(yǎng)液,用PBS洗 1-2次。
2,向瓶?jī)?nèi)加入 1.0-2.0ml 胰蛋白酶液,在倒置顯微鏡下觀察細(xì)胞消化情況,若細(xì)胞大部分變圓,迅速拿回操作臺(tái),吸取胰蛋白酶,加含有 6ml 含 10%血清的培養(yǎng)液,輕輕吹打細(xì)胞。
3,加入等量的的培養(yǎng)液,輕輕吹打混勻后吸出一半,分到新的培養(yǎng)
4,傳代比例:1:2-1:3
七、常見(jiàn)問(wèn)題及解決方案
1、培養(yǎng)瓶有破裂,培養(yǎng)液有漏液:細(xì)胞極大可能會(huì)污染,所以我們會(huì)及時(shí)安排幫老師解決。
2、細(xì)胞漂。号囵B(yǎng)瓶不開封,瓶口酒精擦拭后平躺放置在培養(yǎng)箱。次日觀察,如細(xì)胞大部分又貼回瓶底,表明細(xì)胞活力正常,剩余漂浮的細(xì)胞可以去掉,留 10ml 培養(yǎng)液培養(yǎng)觀察,細(xì)胞生長(zhǎng)至匯合度 80%,進(jìn)行消化傳代;如細(xì)胞還是不貼壁,將細(xì)胞離心收集轉(zhuǎn)到新培養(yǎng)瓶,原培養(yǎng)瓶加部分培養(yǎng)液繼續(xù)培養(yǎng),中間注意觀察,我們的技術(shù)人員會(huì)一直跟蹤指導(dǎo),直到問(wèn)題解決。
細(xì)胞培養(yǎng)代理品牌
細(xì)胞培養(yǎng)代理品牌
| GIBCO 作為細(xì)胞培養(yǎng)的金字招牌,是在此領(lǐng)域的領(lǐng)導(dǎo)者,現(xiàn)在是Invitrogen的一部分。Gibco可以提供*為廣泛的品種以滿足用戶不同的需求,每一種產(chǎn)品都通過(guò)*為嚴(yán)格的品質(zhì)管理。同時(shí),Gibco也可按客戶的要求對(duì)培養(yǎng)基的配方進(jìn)行改動(dòng),或完全按客戶的配方進(jìn)行生產(chǎn)。 |
【虹膜色素上皮細(xì)胞總DNA】齊一生物科技(上海)有限公司是一家專業(yè)生產(chǎn)和銷售各種生化試劑,細(xì)胞株、原代細(xì)胞、菌種、醫(yī)藥中間體,標(biāo)準(zhǔn)品和對(duì)照品的大型化學(xué)科技公司. 齊一生物銷售:021-6034 8496;181214 53965;173021 04490;Web:www.qiyibio.com
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