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Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Capan-2
  • Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Capan-2
  • Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Capan-2
  • Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Capan-2

Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

價(jià)格 詢價(jià)
包裝 1000000Cells/瓶 2000000Cells/瓶
最小起訂量 1000000Cells/瓶
發(fā)貨地 上海
文件下載 檢測(cè)報(bào)告COA
更新日期 2025-02-12
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜英文名稱:Capan-2
品牌: ATCC、DSMZ等產(chǎn)地: 美國(guó)、歐洲、德國(guó)等
保存條件: 低溫避光純度規(guī)格: Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜
產(chǎn)品類別: ATCC細(xì)胞庫(kù)
種屬: 詳見(jiàn)細(xì)胞說(shuō)明書組織: 詳見(jiàn)細(xì)胞說(shuō)明書
細(xì)胞系: 詳見(jiàn)細(xì)胞說(shuō)明書細(xì)胞形態(tài): 詳見(jiàn)細(xì)胞說(shuō)明書
生長(zhǎng)狀態(tài): 詳見(jiàn)細(xì)胞說(shuō)明書靶點(diǎn): 詳見(jiàn)細(xì)胞說(shuō)明書
應(yīng)用: 詳見(jiàn)細(xì)胞說(shuō)明書貨號(hào): 詳見(jiàn)細(xì)胞說(shuō)明書
規(guī)格: 1*10^6cells/T25(1瓶)或1ml凍存管(2支)是否進(jìn)口: 來(lái)源ATCC、DSMZ、ECACC等細(xì)胞庫(kù)
組織來(lái)源: 詳見(jiàn)細(xì)胞說(shuō)明書是否是腫瘤細(xì)胞: 詳見(jiàn)細(xì)胞說(shuō)明書
器官來(lái)源: 詳見(jiàn)細(xì)胞說(shuō)明書品系: 詳見(jiàn)細(xì)胞說(shuō)明書
免疫類型: 詳見(jiàn)細(xì)胞說(shuō)明書物種來(lái)源: 人源或其它動(dòng)物來(lái)源等
保質(zhì)期: 可長(zhǎng)期保存(液氮低溫凍存)
2025-02-12 Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 Capan-2 1000000Cells/瓶/1RMB;2000000Cells/瓶/1RMB 1 ATCC、DSMZ等 美國(guó)、歐洲、德國(guó)等 低溫避光 Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 ATCC細(xì)胞庫(kù)

"Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

傳代比例:1:2-1:4(首次傳代建議1:2)

生長(zhǎng)特性:貼壁生長(zhǎng)

細(xì)胞系的選擇需要考慮到細(xì)胞系的功能特點(diǎn)、生長(zhǎng)速率、鋪板效率、生長(zhǎng)條件和生長(zhǎng)特征、克隆效率、培養(yǎng)方式等因素,如果您想高產(chǎn)量表達(dá)重組蛋白,您可以選擇可以懸浮生長(zhǎng)的快速生長(zhǎng)細(xì)胞系。細(xì)胞培養(yǎng)的操作步驟主要包括傳代、換液、凍存和復(fù)蘇。這些步驟確保了細(xì)胞能夠在實(shí)驗(yàn)室環(huán)境中長(zhǎng)期存活并繼續(xù)增殖。傳代是將細(xì)胞從一個(gè)容器轉(zhuǎn)移到另一個(gè)容器的過(guò)程,以擴(kuò)大細(xì)胞數(shù)量;換液是為了清除代謝廢物并補(bǔ)充新鮮培養(yǎng)基;凍存則是為了長(zhǎng)期保存細(xì)胞,而復(fù)蘇則是重新激活冷凍保存的細(xì)胞使其恢復(fù)正常生長(zhǎng)。

換液周期:每周2-3次

SNU-398 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:NOZ細(xì)胞、LICR-HN-6細(xì)胞、NF639細(xì)胞

NCIH2122 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:4傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:LN-382細(xì)胞、OVTOKO細(xì)胞、NCIH1581細(xì)胞

hs 68 Cells;背景說(shuō)明:該細(xì)胞1969年由Owens RB建立。;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng) ;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MSB1細(xì)胞、MOLP-2細(xì)胞、RBL2H3細(xì)胞

Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息:詳見(jiàn)相關(guān)文獻(xiàn)介紹

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線:1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號(hào)】┈Q┈Q:3┈1┈8┈0┈8┈0┈7┈3┈2┈4;

公司細(xì)胞系主要引進(jìn)ATCC、DSMZ、JCRB、KCLB、RIKEN、ECACC等細(xì)胞庫(kù),細(xì)胞系體外培養(yǎng),它們會(huì)成長(zhǎng)為單層細(xì)胞,附著或緊貼在培養(yǎng)瓶上,或懸浮在體外的溶液中,細(xì)胞系復(fù)蘇周期短,公司細(xì)胞系狀態(tài)良好,飽滿,有光澤等優(yōu)點(diǎn)。EDTA的作用:許多人不用胰酶,只用EDTA,或者用胰酶/EDTA聯(lián)合作用。這里要明白,胰酶切割細(xì)胞外基質(zhì)的一些負(fù)責(zé)粘連和附著的蛋白,而EDTA通過(guò)螯合Ca離子,作用于整聯(lián)蛋白的活性,所以EDTA的作用更加溫和。有的人在胰酶里添加一些EDTA,或者對(duì)付特別難消化的細(xì)胞,添加多一些EDTA,就是這個(gè)道理。一般不要試圖延長(zhǎng)消化時(shí)間(如果10min還消化不下來(lái)的話),而應(yīng)該想其它辦法。

產(chǎn)品包裝:復(fù)蘇發(fā)貨:T25培養(yǎng)瓶(一瓶)或凍存發(fā)貨:1ml凍存管(兩支)

來(lái)源說(shuō)明:細(xì)胞主要來(lái)源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫(kù)

Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來(lái)源:人源、鼠源等其它物種來(lái)源

RGC-6 Cells;背景說(shuō)明:膠質(zhì)細(xì)胞株C6是由Benda等用N-nitrosomethylurea誘導(dǎo)的大鼠膠質(zhì)瘤克隆,并經(jīng)過(guò)一系列的體外培養(yǎng)和動(dòng)物傳代交替后建成的。 當(dāng)細(xì)胞從低密度生長(zhǎng)到滿瓶時(shí),S-100產(chǎn)量增加10倍。;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:RPMI7666細(xì)胞、RKO-AS45-1細(xì)胞、RCC10 RGB細(xì)胞

NFHIOSE-29 Cells;背景說(shuō)明:卵巢;上皮細(xì)胞;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:NCM356細(xì)胞、NCI-H2029細(xì)胞、NCIH1341細(xì)胞

210RCY3-Ag1.2.3 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:C32 [Human melanoma]細(xì)胞、QSG-7701細(xì)胞、NCIH650細(xì)胞

NCI-H1781 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:253JBV細(xì)胞、NHEK細(xì)胞、ESC-410細(xì)胞

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線:1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號(hào)】┈Q┈Q:3┈1┈8┈0┈8┈0┈7┈3┈2┈4;

形態(tài)特性:上皮細(xì)胞樣

細(xì)胞復(fù)蘇相關(guān)注意事項(xiàng):1.取細(xì)胞的過(guò)程中注意帶HAO防凍手套,護(hù)目鏡。此項(xiàng)尤為重要,細(xì)胞凍存管可能漏入,解凍時(shí)凍存管中的氣溫急劇上升,可導(dǎo)致爆炸。2.凍存的問(wèn)題:凍存的配置已是常識(shí),在這里不作詳述,但二甲基亞砜(DMSO )對(duì)細(xì)胞不是完全無(wú)毒副作用,在常溫下,二甲基亞砜對(duì)細(xì)胞的毒副作較大,因此,必須在1-2min內(nèi)使凍存完全融化。如果復(fù)蘇溫度太慢,會(huì)造成細(xì)胞的損傷,二甲基亞砜(DMSO)ZuiHAO選擇進(jìn)口產(chǎn)品。3.離心前須加入少量培養(yǎng)。細(xì)胞解凍后二甲基亞砜濃度較GAO,注意加入少量培養(yǎng)可稀釋其濃度,以減少對(duì)細(xì)胞的損傷。4.離心問(wèn)題:目前主要有兩種見(jiàn)解。一種是解凍后的細(xì)胞懸直接吹打均勻后分裝到培養(yǎng)瓶中進(jìn)行培養(yǎng),第二天換。因?yàn)殡x心的目的是兩個(gè),去除DMSO,去除死細(xì)胞,這個(gè)是標(biāo)準(zhǔn)流程,但對(duì)一般人來(lái)說(shuō),把握不HAO離心轉(zhuǎn)速和時(shí)間,轉(zhuǎn)的不夠活細(xì)胞沉底的少,細(xì)胞就全被扔掉了,轉(zhuǎn)過(guò)了活細(xì)胞會(huì)受壓過(guò)大,死亡。此外在操作過(guò)程中容易污染,所以不推薦。另一種說(shuō)法為細(xì)胞懸中含有二甲基亞砜(DMSO),DMSO對(duì)細(xì)胞有一定的毒副作用,所以須將離心后的體前倒凈,且一定倒干凈。我在試驗(yàn)中按照常規(guī)的離心分裝的方法進(jìn)行復(fù)蘇,結(jié)果無(wú)異常。5.細(xì)胞貼壁少的問(wèn)題:教科書中說(shuō)明凍存細(xì)胞解凍時(shí)1ml細(xì)胞要加10ml-15ml培養(yǎng),而在我的試驗(yàn)中的經(jīng)驗(yàn)總結(jié)為培養(yǎng)基越少細(xì)胞越容易貼附。6.復(fù)蘇細(xì)胞分裝的問(wèn)題:試驗(yàn)中我的經(jīng)驗(yàn)總結(jié)為復(fù)蘇1管細(xì)胞一般可分裝到1-2只培養(yǎng)瓶中,分裝過(guò)多,細(xì)胞濃度過(guò)低,不利于細(xì)胞的貼壁。7.加培養(yǎng)基的量放入問(wèn)題:這個(gè)量的多少的把握主要涉及到的問(wèn)題DMSO的濃度,從如果你加培養(yǎng)基的太少,那么DMSO的濃度就會(huì)比較大,就會(huì)影響細(xì)胞生長(zhǎng),從以前的資料來(lái)看,DMSO的濃度在小于0.5%的時(shí)候?qū)σ话慵?xì)胞沒(méi)有什么影響,還有一個(gè)說(shuō)法是1%。所以如果你的凍存的濃度是10%DMSO的話那么加10ml以上的培養(yǎng)基就恰HAO稀釋到了無(wú)害濃度。

C8-D1A Cells;背景說(shuō)明:該永生化細(xì)胞系源自出生8天小鼠小腦組織,由B Pessac, D Trisler建立。該細(xì)胞具有小神經(jīng)膠質(zhì)細(xì)胞特征。該細(xì)胞為GFAP陽(yáng)性細(xì)胞,除此之外,沒(méi)有檢測(cè)到其它神經(jīng)膠質(zhì)神經(jīng)元或小神經(jīng)膠質(zhì)細(xì)胞的分子標(biāo)記。;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng) ;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MN9D細(xì)胞、CCRF CEM細(xì)胞、CSQT-2細(xì)胞

SJRH30 Cells;背景說(shuō)明:肺泡橫紋肌肉瘤;骨髓轉(zhuǎn)移;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:HMEL細(xì)胞、SKOV3細(xì)胞、WEHI 164 TC細(xì)胞

CEMC7 Cells;背景說(shuō)明:急性T淋巴細(xì)胞白血病;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:HPDLF細(xì)胞、Jijoye細(xì)胞、H.Ep. #2細(xì)胞

OVCAR432 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:LU-65M細(xì)胞、Malme-3M細(xì)胞、H-2030細(xì)胞

PANC-1 Cells;背景說(shuō)明:這株人胰腺癌細(xì)胞株源自于胰腺癌導(dǎo)管細(xì)胞,其倍增時(shí)間為52小時(shí)。染色體研究表明,該細(xì)胞染色體眾數(shù)為63,包括3個(gè)獨(dú)特標(biāo)記的染色體和1個(gè)小環(huán)狀染色體。該細(xì)胞的生長(zhǎng)可被1unit/ml的左旋天冬酰胺酶抑制;能在軟瓊脂上生長(zhǎng);能在裸鼠上成瘤。;傳代方法:1:2-1:4傳代;每周2-3次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;多角形;相關(guān)產(chǎn)品有:HIEC-6細(xì)胞、HIT T15細(xì)胞、Leghorn Male Hepatoma cell line細(xì)胞

JJN3 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:DrG細(xì)胞、SK-RC 39細(xì)胞、MiaPaca.2細(xì)胞

P-19 Cells;背景說(shuō)明:P19細(xì)胞株是從C3H/He小鼠中誘導(dǎo)的惡性畸胎瘤中建立的。該細(xì)胞在含有0.1mM的培養(yǎng)基中可高效率地克隆。該細(xì)胞具有多能性,在500nM維A酸誘導(dǎo)下可以分化成神經(jīng)和神經(jīng)膠質(zhì)樣細(xì)胞;在0.5%~1.0%二甲亞砜(DMSO)存在下,分化形成心臟和骨骼肌樣細(xì)胞,但不形成神經(jīng)或神經(jīng)膠質(zhì)樣細(xì)胞;在DMSO和維A酸同時(shí)存在時(shí),細(xì)胞的分化與只有維A酸一樣。;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:HPAF/CD18細(xì)胞、184A1細(xì)胞、Spodoptera frugiperda clone 9細(xì)胞

ZYM-SVEC01 Cells;背景說(shuō)明:靜脈血管內(nèi)皮 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:EB-1細(xì)胞、HOS-143B細(xì)胞、KTCTL-140細(xì)胞

P 815 Cells;背景說(shuō)明:肥大細(xì)胞瘤;雄性;DBA/2;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SPCA1細(xì)胞、SNU354細(xì)胞、EU-3細(xì)胞

MNNG Cells;背景說(shuō)明:骨肉瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:I90細(xì)胞、Clone 929細(xì)胞、SW 839細(xì)胞

P388.D1 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SKHEP1細(xì)胞、BT 549細(xì)胞、U-87MG ATCC細(xì)胞

M14-MEL Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3傳代;生長(zhǎng)特性:混合生長(zhǎng);形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MDA-MB 361細(xì)胞、SW982細(xì)胞、CCD-966SK細(xì)胞

DMS 273 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:AN-3細(xì)胞、OCI-Ly7細(xì)胞、Hs940-T細(xì)胞

M-14 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3傳代;生長(zhǎng)特性:混合生長(zhǎng);形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SW626細(xì)胞、NIH 3T6細(xì)胞、BNL-CL.2細(xì)胞

Kit 225-K6 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:3T3-F442A細(xì)胞、PIEC細(xì)胞、SK-MEL-3細(xì)胞

SK.MEL.28 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:8?jìng)鞔?,?3天換液1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:星形的;相關(guān)產(chǎn)品有:H-1770細(xì)胞、U-251細(xì)胞、Z138細(xì)胞

MDA-MB-415 Cells;背景說(shuō)明:這株細(xì)胞表達(dá)WNT7B癌基因。8168088].帶瘤患者來(lái)自巴拉圭,雖然填報(bào)的是白人,但細(xì)胞表型存在G6PDA型,顯示其屬于混血。細(xì)胞株形成平展延伸的上皮細(xì)胞樣,在電鏡下呈現(xiàn)結(jié)節(jié),伴隨著延伸的微管和微板。不容易用胰酶消化。;傳代方法:消化5-10分鐘。1:2。4-5天長(zhǎng)滿。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:NCI.H23細(xì)胞、QSG7701細(xì)胞、H-1930細(xì)胞

Abcam A-549 MSI1 KO Cells(提供STR鑒定圖譜)

Abeomics CHO-K1 SIGLEC5 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSG336 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRU200 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC719 Cells(提供STR鑒定圖譜)

CHO-AS52 Cells(提供STR鑒定圖譜)

DA02457 Cells(提供STR鑒定圖譜)

DA04796 Cells(提供STR鑒定圖譜)

FS6-14.13 Cells(提供STR鑒定圖譜)

FRO 81-2 Cells;背景說(shuō)明:未分化甲狀腺癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:hTERT-RPE1細(xì)胞、Ect1/E6E7細(xì)胞、IMCD3細(xì)胞

Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

NCIH1819 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:CW2細(xì)胞、SUM52PE細(xì)胞、SVEC 4-10細(xì)胞

Colon-38 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:CEM/0細(xì)胞、786-0WT細(xì)胞、LTEP-s細(xì)胞

Wills Eye Research Institute-Retinoblastoma-1 Cells;背景說(shuō)明:WERI-Rb-I細(xì)胞株是1974年R.M. McFall 和 T.W. Sery建立的兩株人眼癌細(xì)胞系中的一株。 細(xì)胞能在Difco Bacto-Agar中存活但不形成克隆。 掃描電鏡顯示在表面囊泡,板狀偽足和微絨毛在數(shù)量上和頻率上的改變。 細(xì)胞分化研究,腫瘤治療的動(dòng)物模型和生化評(píng)價(jià)都涉及這株細(xì)胞。;傳代方法:消化3-5分鐘。1:2。3天內(nèi)可長(zhǎng)滿。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:圓形細(xì)胞聚集成葡萄狀;相關(guān)產(chǎn)品有:18G3.cl 1細(xì)胞、NCIH226細(xì)胞、Pa16C細(xì)胞

686LN-M4e Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:HSC-2細(xì)胞、Dx5細(xì)胞、786-O RCC細(xì)胞

OPM2 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:KP-N-YN細(xì)胞、SKRC 39細(xì)胞、RSC-364細(xì)胞

12.1 [Mouse hybridoma against human CD6] Cells(提供STR鑒定圖譜)

H-157 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng) ;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:U266 B1細(xì)胞、NCI-H1876細(xì)胞、Panc10.05細(xì)胞

Panc203 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:SCH細(xì)胞、HCASMC細(xì)胞、Human podocyte細(xì)胞

NCIH187 Cells;背景說(shuō)明:經(jīng)典小細(xì)胞肺癌;胸腔積液轉(zhuǎn)移;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:J774.A1細(xì)胞、CMT.64細(xì)胞、HMEC1細(xì)胞

SN12C-PM6 Cells;背景說(shuō)明:腎癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:NBL-5細(xì)胞、SK-N-FI細(xì)胞、Strain KB細(xì)胞

H-522 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:6傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:HEK-293-F細(xì)胞、HTR8/SVneo細(xì)胞、H-1703細(xì)胞

OSK-1 Cells;背景說(shuō)明:誘導(dǎo)型多能干 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:REC-1細(xì)胞、Pro-5 Lec1.3c細(xì)胞、A-549細(xì)胞

HFL1 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:消化3-5分鐘。1:2。3天內(nèi)可長(zhǎng)滿。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:MC3T3細(xì)胞、COLO-684細(xì)胞、SKO-007細(xì)胞

Ku812F Cells;背景說(shuō)明:慢性粒細(xì)胞白血?。荒行?傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:159PT細(xì)胞、GC-2細(xì)胞、CD-18細(xì)胞

GW0012 Cells(提供STR鑒定圖譜)

HAP1 PRKD1 (-) 2 Cells(提供STR鑒定圖譜)

SU4 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:NW38細(xì)胞、MCA-38細(xì)胞、CAL-39細(xì)胞

HT-1080 Cells;背景說(shuō)明:該細(xì)胞源自一名35歲患有纖維肉瘤的白人男性的結(jié)締組織;ras+。;傳代方法:1:4-1:8?jìng)鞔?;?3天換液1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:AMJ2C8細(xì)胞、Capan-2細(xì)胞、U266細(xì)胞

SKG-IIIa Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:2x10^4 cells/ml;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:IOSE80細(xì)胞、BC-019細(xì)胞、H-2196細(xì)胞

NCI-H510A Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:8?jìng)鞔?;每周換液2次。;生長(zhǎng)特性:混合生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:G-292 clone A141B1細(xì)胞、H209細(xì)胞、CL1.0細(xì)胞

HuTu 80 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2—1:5傳代,每周換液2-3次;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:BT483細(xì)胞、MPC-83細(xì)胞、Nakata-1細(xì)胞

Stanford University-Diffuse Histiocytic Lymphoma-16 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:EFM19細(xì)胞、DHL-2細(xì)胞、U937細(xì)胞

U2OS Cells;背景說(shuō)明:骨肉瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Hela-Ap-1細(xì)胞、BIU-87細(xì)胞、KLN-205細(xì)胞

KRC/Y Cells;背景說(shuō)明:腎透明細(xì)胞癌;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:VMM5細(xì)胞、GT1-1細(xì)胞、P31/FUJ細(xì)胞

HUES 59 Cells(提供STR鑒定圖譜)

L-428 Cells(提供STR鑒定圖譜)

MSC G-CSF#1 Cells(提供STR鑒定圖譜)

OCUU-6 Cells(提供STR鑒定圖譜)

RNJ12 Cells(提供STR鑒定圖譜)

Ubigene HEK293 CSNK1G2 KO Cells(提供STR鑒定圖譜)

WG0067 Cells(提供STR鑒定圖譜)

HCS-TG C3 Cells(提供STR鑒定圖譜)

3T3 Swiss Albino Cells;背景說(shuō)明:3T3細(xì)胞株是1962年Todaro G和Green H從分離的瑞士小鼠胚胎中建立的;該細(xì)胞的生長(zhǎng)受接觸性抑制,匯合狀態(tài)的單層細(xì)胞密度為40000個(gè)細(xì)胞/平方厘米;檢測(cè)結(jié)果顯示該細(xì)胞鼠痘病毒陰性;在中生長(zhǎng)較好,在某些玻璃表面上可能狀態(tài)不佳;細(xì)胞生長(zhǎng)飽和時(shí)其密度可以達(dá)到約50000 cells/cm2。;傳代方法:1:3傳代;3-4天1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:OVTOKO細(xì)胞、BNL CL2細(xì)胞、CCK81細(xì)胞

AZ 521 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:4傳代;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:A72細(xì)胞、H1651細(xì)胞、U-343-MG細(xì)胞

MeT-5A Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:A-549細(xì)胞、SK-ES1細(xì)胞、PANC 327細(xì)胞

HMEC-1 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:LICCF細(xì)胞、5637細(xì)胞、APRE-19細(xì)胞

P3/X63-Ag8 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MHCC 97細(xì)胞、MOVAS細(xì)胞、HCC-366細(xì)胞

P3/X63-Ag8 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MHCC 97細(xì)胞、MOVAS細(xì)胞、HCC-366細(xì)胞

Leukemia L1210 Cells;背景說(shuō)明:該細(xì)胞源于用0.2%甲基膽蒽(溶解)涂抹雌性小鼠的皮膚誘發(fā)的腫瘤,鼠痘病毒陰性。;傳代方法:1:2傳代;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:Normal Rat, August 3, 1983細(xì)胞、NCI.H226細(xì)胞、HCGC細(xì)胞

HF-91 Cells;背景說(shuō)明:成纖維 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:TE-7細(xì)胞、10T1/2細(xì)胞、Ramos-RA1細(xì)胞

MOLT16 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:J774A1細(xì)胞、NCIH292細(xì)胞、NeHepLxHT細(xì)胞

NB4 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Hep G2細(xì)胞、H524細(xì)胞、COR-L105細(xì)胞

P31/Fujioka Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:5傳代;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:B958細(xì)胞、SK BR 03細(xì)胞、D562細(xì)胞

P-388D1 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:OV1063細(xì)胞、L-Wnt3A細(xì)胞、Neuro 2a細(xì)胞

NCI-H250 Cells;背景說(shuō)明:小細(xì)胞肺癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:半貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H-295細(xì)胞、H1341細(xì)胞、NCI-H226細(xì)胞

H2073 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:6傳代 ;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:253J B-V細(xì)胞、CSQT-2細(xì)胞、McA-RH8994細(xì)胞

LS-180 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:COLO678細(xì)胞、ABC1細(xì)胞、K1735細(xì)胞

SZ-BRCA1-4 Cells(提供STR鑒定圖譜)

BHP10-3 Cells;背景說(shuō)明:甲狀腺乳頭狀癌;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:A375-SM細(xì)胞、MES23.5細(xì)胞、SKGT2細(xì)胞

HS0578T Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:L cells (TK-)細(xì)胞、TK 10細(xì)胞、MGc80-3細(xì)胞

NKM-1 Cells;背景說(shuō)明:急性髓系白血??;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:ZYM-SVEC01細(xì)胞、SCL-1細(xì)胞、Roswell Park Memorial Institute 1788細(xì)胞

NRK clone 49F Cells;背景說(shuō)明:腎;成纖維細(xì)胞;自發(fā)永生;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H322T細(xì)胞、OVCA-420細(xì)胞、OE21細(xì)胞

A10 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SK-MEL2細(xì)胞、alphaTC clone 6細(xì)胞、OV90細(xì)胞

H196 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:4-1:6傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:WM-2664細(xì)胞、HcaF細(xì)胞、GM01232細(xì)胞

Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

SK-MEL2 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:6傳代,2-3天換液1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:多邊形的;相關(guān)產(chǎn)品有:COLO824細(xì)胞、NCIH2286細(xì)胞、NBL-2細(xì)胞

RCC4 Cells;背景說(shuō)明:腎透明細(xì)胞癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:KM933細(xì)胞、NCI-SNU-423細(xì)胞、HEK 293-F細(xì)胞

P3 NS1 Ag4 Cells;背景說(shuō)明:這是P3X63Ag8(ATCCTIB-9)的一個(gè)不分泌克隆。Kappa鏈合成了但不分泌。能抗0.1mM8-氮雜鳥(niǎo)嘌呤但不能在HAT培養(yǎng)基中生長(zhǎng)。據(jù)報(bào)道它是由于缺失了3-酮類固醇還原酶活性的膽固醇營(yíng)養(yǎng)缺陷型。檢測(cè)表明肢骨發(fā)育畸形病毒(鼠痘)陰性。;傳代方法:1:2傳代,3天內(nèi)可長(zhǎng)滿。;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:Hs 706.T細(xì)胞、National Medical Center-Glioma 1細(xì)胞、RCC-10細(xì)胞

Earle's L cells Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MGECs細(xì)胞、SKBR-3細(xì)胞、MDCC MSB1細(xì)胞

COR-L 105 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:CHP212細(xì)胞、CHL細(xì)胞、67NR細(xì)胞

HLFa Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:4傳代;每周換液2次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成纖維細(xì)胞;相關(guān)產(chǎn)品有:H1563細(xì)胞、LoVo細(xì)胞、MBdSMC細(xì)胞

H-2452 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:消化3-5分鐘。1:2。3天內(nèi)可長(zhǎng)滿。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:C-8161細(xì)胞、HCC2218細(xì)胞、COV-434細(xì)胞

SNK-6 Cells;背景說(shuō)明:NK/T細(xì)胞淋巴瘤;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:L cells細(xì)胞、P560細(xì)胞、MonoMac1細(xì)胞

BayGenomics ES cell line CSI146 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RST353 Cells(提供STR鑒定圖譜)

C-26 Cells(提供STR鑒定圖譜)

L91.7 Cells(提供STR鑒定圖譜)

Psi-CRIP-MFGhM-CSF Cells(提供STR鑒定圖譜)

RE 6 Cells(提供STR鑒定圖譜)

" "PubMed=3019537

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Mutations and altered expression of p16INK4 in human cancer.

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Comparative analysis of mutations in the p53 and K-ras genes in pancreatic cancer.

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Specific chromosomal aberrations and amplification of the AIB1 nuclear receptor coactivator gene in pancreatic carcinomas.

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Loss of the Y chromosome is a frequent chromosomal imbalance in pancreatic cancer and allows differentiation to chronic pancreatitis.

Int. J. Cancer 91:340-344(2001)


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Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.

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Iacobuzio-Donahue C.A., Ashfaq R., Maitra A., Adsay N.V., Shen-Ong G.L.-C., Berg K., Hollingsworth M.A., Cameron J.L., Yeo C.J., Kern S.E., Goggins M.G., Hruban R.H.

Highly expressed genes in pancreatic ductal adenocarcinomas: a comprehensive characterization and comparison of the transcription profiles obtained from three major technologies.

Cancer Res. 63:8614-8622(2003)


PubMed=15126341; DOI=10.1158/0008-5472.CAN-03-3159

Heidenblad M., Schoenmakers E.F.P.M., Jonson T., Gorunova L., Veltman J.A., van Kessel A.G., Hoglund M.

Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.

Cancer Res. 64:3052-3059(2004)


PubMed=15367885; DOI=10.1097/00006676-200410000-00004

Loukopoulos P., Kanetaka K., Takamura M., Shibata T., Sakamoto M., Hirohashi S.

Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.

Pancreas 29:193-203(2004)


PubMed=15688027; DOI=10.1038/sj.onc.1208383

Heidenblad M., Lindgren D., Veltman J.A., Jonson T., Mahlamaki E.H., Gorunova L., van Kessel A.G., Schoenmakers E.F.P.M., Hoglund M.

Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.

Oncogene 24:1794-1801(2005)


PubMed=15770730; DOI=10.3748/wjg.v11.i10.1521; PMCID=PMC4305696

Ma J.-H., Patrut E., Schmidt J., Knaebel H.-P., Buchler M.W., Marten A.

Synergistic effects of interferon-alpha in combination with chemoradiation on human pancreatic adenocarcinoma.

World J. Gastroenterol. 11:1521-1528(2005)


PubMed=18298655; DOI=10.1111/j.1582-4934.2008.00289.x; PMCID=PMC3828895

Pilarsky C., Ammerpohl O., Sipos B., Dahl E., Hartmann A., Wellmann A., Braunschweig T., Lohr J.-M., Jesenofsky R., Friess H., Wente M.N., Kristiansen G., Jahnke B., Denz A., Ruckert F., Schackert H.K., Kloppel G., Kalthoff H., Saeger H.-D., Grutzmann R.

Activation of Wnt signalling in stroma from pancreatic cancer identified by gene expression profiling.

J. Cell. Mol. Med. 12:2823-2835(2008)


PubMed=18380791; DOI=10.1111/j.1349-7006.2008.00779.x; PMCID=PMC11158928

Suzuki A., Shibata T., Shimada Y., Murakami Y., Horii A., Shiratori K., Hirohashi S., Inazawa J., Imoto I.

Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization.

Cancer Sci. 99:986-994(2008)


CLPUB00416

Oberlin L.

Treatment of pancreatic carcinoma cell lines in vitro and vivo with a monoclonal antibody against the transferrin receptor.

Thesis VMD (2009); Justus-Liebig-Universitat Giessen; Giessen; Germany


DOI=10.4172/jpb.1000057

Yamada M., Fujii K., Koyama K., Hirohashi S., Kondo T.

The proteomic profile of pancreatic cancer cell lines corresponding to carcinogenesis and metastasis.

J. Proteomics Bioinformatics 2:1-18(2009)


PubMed=20037478; DOI=10.4161/cbt.8.21.9685; PMCID=PMC2824894

Kent O.A., Mullendore M.E., Wentzel E.A., Lopez-Romero P., Tan A.-C., Alvarez H., West K.M., Ochs M.F., Hidalgo M., Arking D.E., Maitra A., Mendell J.T.

A resource for analysis of microRNA expression and function in pancreatic ductal adenocarcinoma cells.

Cancer Biol. Ther. 8:2013-2024(2009)


PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113

Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

Signatures of mutation and selection in the cancer genome.

Nature 463:893-898(2010)


PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662

Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.

A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.

Cancer Res. 70:2158-2164(2010)


PubMed=20418756; DOI=10.1097/MPA.0b013e3181c15963; PMCID=PMC2860631

Deer E.L., Gonzalez-Hernandez J., Coursen J.D., Shea J.E., Ngatia J.G., Scaife C.L., Firpo M.A., Mulvihill S.J.

Phenotype and genotype of pancreatic cancer cell lines.

Pancreas 39:425-435(2010)


PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027

Barretina J.G., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehar J., Kryukov G.V., Sonkin D., Reddy A., Liu M., Murray L., Berger M.F., Monahan J.E., Morais P., Meltzer J., Korejwa A., Jane-Valbuena J., Mapa F.A., Thibault J., Bric-Furlong E., Raman P., Shipway A., Engels I.H., Cheng J., Yu G.-Y.K., Yu J.-J., Aspesi P. Jr., de Silva M., Jagtap K., Jones M.D., Wang L., Hatton C., Palescandolo E., Gupta S., Mahan S., Sougnez C., Onofrio R.C., Liefeld T., MacConaill L.E., Winckler W., Reich M., Li N.-X., Mesirov J.P., Gabriel S.B., Getz G., Ardlie K., Chan V., Myer V.E., Weber B.L., Porter J., Warmuth M., Finan P., Harris J.L., Meyerson M.L., Golub T.R., Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.

The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.

Nature 483:603-607(2012)


PubMed=22585861; DOI=10.1158/2159-8290.CD-11-0224; PMCID=PMC5057396

Marcotte R., Brown K.R., Suarez Saiz F.J., Sayad A., Karamboulas K., Krzyzanowski P.M., Sircoulomb F., Medrano M., Fedyshyn Y., Koh J.L.-Y., van Dyk D., Fedyshyn B., Luhova M., Brito G.C., Vizeacoumar F.J., Vizeacoumar F.S., Datti A., Kasimer D., Buzina A., Mero P., Misquitta C., Normand J., Haider M., Ketela T., Wrana J.L., Rottapel R., Neel B.G., Moffat J.

Essential gene profiles in breast, pancreatic, and ovarian cancer cells.

Cancer Discov. 2:172-189(2012)


PubMed=24700732; DOI=10.1002/humu.22556; PMCID=PMC4451114

Leroy B., Girard L., Hollestelle A., Minna J.D., Gazdar A.F., Soussi T.

Analysis of TP53 mutation status in human cancer cell lines: a reassessment.

Hum. Mutat. 35:756-765(2014)


PubMed=25167228; DOI=10.1038/bjc.2014.475; PMCID=PMC4453732

Hamidi H., Lu M., Chau K., Anderson L., Fejzo M.S., Ginther C., Linnartz R., Zubel A., Slamon D.J., Finn R.S.

KRAS mutational subtype and copy number predict in vitro response of human pancreatic cancer cell lines to MEK inhibition.

Br. J. Cancer 111:1788-1801(2014)


PubMed=25485619; DOI=10.1038/nbt.3080

Klijn C., Durinck S., Stawiski E.W., Haverty P.M., Jiang Z.-S., Liu H.-B., Degenhardt J., Mayba O., Gnad F., Liu J.-F., Pau G., Reeder J., Cao Y., Mukhyala K., Selvaraj S.K., Yu M.-M., Zynda G.J., Brauer M.J., Wu T.D., Gentleman R.C., Manning G., Yauch R.L., Bourgon R., Stokoe D., Modrusan Z., Neve R.M., de Sauvage F.J., Settleman J., Seshagiri S., Zhang Z.-M.

A comprehensive transcriptional portrait of human cancer cell lines.

Nat. Biotechnol. 33:306-312(2015)


PubMed=25877200; DOI=10.1038/nature14397

Yu M., Selvaraj S.K., Liang-Chu M.M.Y., Aghajani S., Busse M., Yuan J., Lee G., Peale F.V., Klijn C., Bourgon R., Kaminker J.S., Neve R.M.

A resource for cell line authentication, annotation and quality control.

Nature 520:307-311(2015)


PubMed=26216984; DOI=10.1073/pnas.1501605112; PMCID=PMC4538616

Daemen A., Peterson D., Sahu N., McCord R., Du X.-N., Liu B., Kowanetz K., Hong R., Moffat J., Gao M., Boudreau A., Mroue R., Corson L., O'Brien T., Qing J., Sampath D., Merchant M., Yauch R.L., Manning G., Settleman J., Hatzivassiliou G., Evangelista M.

Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors.

Proc. Natl. Acad. Sci. U.S.A. 112:E4410-E4417(2015)


PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878

Scholtalbers J., Boegel S., Bukur T., Byl M., Goerges S., Sorn P., Loewer M., Sahin U., Castle J.C.

TCLP: an online cancer cell line catalogue integrating HLA type, predicted neo-epitopes, virus and gene expression.

Genome Med. 7:118.1-118.7(2015)


PubMed=27259358; DOI=10.1074/mcp.M116.058313; PMCID=PMC4974343

Humphrey E.S., Su S.-P., Nagrial A.M., Hochgrafe F., Pajic M., Lehrbach G.M., Parton R.G., Yap A.S., Horvath L.G., Chang D.K., Biankin A.V., Wu J.-M., Daly R.J.

Resolution of novel pancreatic ductal adenocarcinoma subtypes by global phosphotyrosine profiling.

Mol. Cell. Proteomics 15:2671-2685(2016)


PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469

Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

A landscape of pharmacogenomic interactions in cancer.

Cell 166:740-754(2016)


PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675

Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.

An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.

Cancer Res. 79:1263-1273(2019)"


關(guān)鍵字: Capan-2人胰腺癌細(xì)胞代次低|培養(yǎng)基;復(fù)蘇細(xì)胞系;細(xì)胞STR鑒定報(bào)告;細(xì)胞STR鑒定圖譜;ATCC|DSMZ細(xì)胞庫(kù);

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