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簡(jiǎn)要描述:大鼠腸上皮細(xì)胞收到后首先觀察細(xì)胞瓶是否完好,培養(yǎng)液是否有漏液、渾濁等現(xiàn)象,若有上述現(xiàn)象發(fā)生請(qǐng)及時(shí)和我們。仔細(xì)閱讀細(xì)胞說(shuō)明書,了解細(xì)胞相關(guān)信息,如細(xì)胞形態(tài)、所用培養(yǎng)基、血清比例、所需細(xì)胞因子等。
產(chǎn)品型號(hào): 1ml/株
所屬分類:大鼠原代細(xì)胞
更新時(shí)間:2024-12-23
大鼠腸上皮細(xì)胞培養(yǎng)條件:DMEM(高糖)+10%FBS,傳代方法:按1:3傳代,凍存條件:90%FBS+10%DMSO,規(guī)格:25T,產(chǎn)品復(fù)蘇率:60培養(yǎng)兩天就能清晰看到軸突與樹(shù)突,培養(yǎng)時(shí)間可長(zhǎng)達(dá)13-16天,質(zhì)量控制:嚴(yán)格經(jīng)過(guò)了細(xì)菌、真菌、霉菌、病毒(HIV、HBV、HCV)、支原體檢測(cè),產(chǎn)品庫(kù)存:現(xiàn)貨供應(yīng)。
大鼠腸上皮細(xì)胞具體操作:
1).首先不加*,倒掉舊培養(yǎng)基加入少量新培養(yǎng)基洗1-2遍,(這是前奏,即為*步,目的是將漂浮著的死細(xì)胞之類盡量洗掉。
2).然后再加入少量新培養(yǎng)基直接吹打一遍,這一遍是把貼壁不牢固的細(xì)胞吹打下來(lái)。再用培養(yǎng)基洗一遍,兩次所得懸液混合傳入新瓶。即為第二步(你可以將這些傳入新瓶培養(yǎng),以與后面*消化過(guò)的細(xì)胞對(duì)比觀察看誰(shuí)長(zhǎng)的更好一點(diǎn)就知道該細(xì)胞對(duì)*的敏感度了。)
3).吸干凈瓶?jī)?nèi)剩余液體,加入0.3ml左右的*潤(rùn)洗一遍,吸掉棄之,再加入1ml左右的*消化。消化的同時(shí)置于顯微鏡下觀察,待細(xì)胞與細(xì)胞之間間隙明顯的時(shí)候立即吸掉*與干凈彈頭里備用,加入新培養(yǎng)基開(kāi)始吹打,吹打2-3遍后吸取懸液于試管或新瓶暫存。用2ml左右新培養(yǎng)基洗一遍與前面的混合。(你也可以傳入新瓶培養(yǎng),以與后面及前面的做對(duì)比。)這是第三步。
4).然后把前面剛吸出來(lái)的*重新加進(jìn)去瓶里繼續(xù)消化剩余的貼壁牢固的細(xì)胞。當(dāng)然你也可以用新的*,如果你們那比較富裕的話,呵呵。繼續(xù)鏡下觀察,待剩余細(xì)胞間隙明顯,細(xì)胞獨(dú)立開(kāi)來(lái)的時(shí)候,吸掉*,加入新培養(yǎng)基吹打。懸液傳入新瓶培養(yǎng)(根據(jù)實(shí)際情況你自己把握)。這是第四步。
其實(shí)還可以有第五步,對(duì)于特別難消化的細(xì)胞和對(duì)*特別敏感的細(xì)胞的話,你可以繼續(xù)加第五步甚至第六步。為了細(xì)胞更好的狀態(tài),更漂亮的樣子,沒(méi)辦法,你必須分多批多次消化,這樣才能zui大限度地將*對(duì)細(xì)胞的損傷降到zui低,保證細(xì)胞的狀態(tài)能夠*。
xy1378 STEMium 人胚胎干細(xì)胞無(wú)血清培養(yǎng)基 Human Pluripotent Stem Cell Growth Medium 500 ml
xy1379 STEMium-XF 無(wú)異種人胚胎干細(xì)胞生長(zhǎng)培養(yǎng)基 Xeno-free Human Pluripotent Stem Cell Growth Medium 500 ml
xy1380 MEF-cm 小鼠胚胎成纖維細(xì)胞培養(yǎng)基 Mouse Embryonic Fibroblasts-Conditioned Medium 100 ml
xy1381 bFGF-std MEF-cm 堿性成纖維細(xì)胞生長(zhǎng)因子刺激的小鼠胚胎成纖維細(xì)胞條件培養(yǎng)基 bFGF-Stimulated Mouse Embryonic Fibroblasts Conditioned Medium 100ml
xy1382 CEpiCM 角膜上皮細(xì)胞培養(yǎng)基 Corneal Epithelial Cell Medium 500 ml
xy1383 OEpiCM 卵巢上皮細(xì)胞培養(yǎng)基 Ovarian Epithelial Cell Medium 500 ml
xy1384 MSCM-sf 間充質(zhì)干細(xì)胞培養(yǎng)基 Mesenchymal Stem Cell Medium-serum free 500 ml
xy1385 MEpiCM 乳腺上皮細(xì)胞培養(yǎng)基 Mammary Epithelial Cell Medium 500 ml
xy1386 KM-acf 角質(zhì)細(xì)胞培養(yǎng)基 Keratinocyte Medium-animal component free 500 ml
xy1387 FM-acf 成纖維細(xì)胞培養(yǎng)基 Fibroblast Medium-animal component free 500 ml
xy1388 STEMium-ACF 人類多能干細(xì)胞培養(yǎng)基-無(wú)動(dòng)物組分 STEMium Human Pluripotent Stem Cell Growth Medium-animal component free 500ml
xy1389 MSCM-acf 間充質(zhì)干細(xì)胞培養(yǎng)基 Mesenchymal Stem Cell Medium-animal component free 500 ml
xy1390 MEM MEM MEM with Earle's Salts and L-Glutamine 500 ml
xy1391 MEM MEM MEM with Hank's Salts and L-Glutamine 500 ml
xy1392 MEM MEM MEM with Eagles's Salts and Glutamine 500 ml
xy1393 M199E M199E Medium 199 with Earle's Salts and L-Glutamine 500 ml
xy1394 M199H M199H Medium 199 with Hanks Salts and L-Glutamine 500 ml
xy1395 DMEM DMEM DMEM with L-Glutamine and Sodium Pyruvate 500 ml
xy1396 DMEM DMEM DMEM with High-Glucose - L-Glutamine and Sodium Pyruvate 500 ml
xy1397 DMEM DMEM DMEM with High-Glucose - L-Glutamine and Sodium Pyruvate 1L
xy1398 DMEM DMEM DMEM with L-Glutamine - Sodium Pyruvate and 25 mM HEPES 500 ml
xy1399 DMEM DMEM DMEM with High-Glucose - L-Glutamine - Sodium Pyruvate and 25 mM HEPES 500 ml
xy1400 DMEM-prf DMEM-prf DMEM with High Glucose - L-Glutamine and Sodium Pyruvate - phenol red-free 1L
xy1401 Ham's F-10 Ham's F-10 F-10 with L-Glutamine and 25 mM HEPES 500 ml
xy1402 Ham's F-12 Ham's F-12 F-12 with L-Glutamine and 25 mM HEPES 500 ml
xy1403 DMEM/F-12 DMEM/F-12 DMEM/F-12 with L-Glutamine 500 ml
xy1404 DMEM/F-12 DMEM/F-12 DMEM/F-12 with L-Glutamine and 15 mM HEPES 500 ml
xy1405 RPMI 1640 RPMI 1640 RPMI 1640 without L-Glutamine - with 25 mM HEPES 500 ml
xy1406 RPMI 1640 RPMI 1640 RPMI 1640 with L-Glutamine and 25 mM HEPES 500 ml
xy1407 IMDM IMDM MDM with L-Glutamine and 25 mM HEPES; without alpha-Thioglycerol - 2-mercaptoethanol 500 ml
xy1408 rhSCF 重組人干細(xì)胞因子 Recombinant Human Stem Cell Factor 2μg