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AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,AsPC-1
  • AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,AsPC-1
  • AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,AsPC-1
  • AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,AsPC-1

AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

價格 詢價
包裝 1000000Cells/瓶 2000000Cells/瓶
最小起訂量 1000000Cells/瓶
發(fā)貨地 上海
文件下載 檢測報告COA
更新日期 2025-02-07
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜英文名稱:AsPC-1
品牌: ATCC、DSMZ等產(chǎn)地: 美國、歐洲、德國等
保存條件: 低溫避光純度規(guī)格: AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜
產(chǎn)品類別: ATCC細(xì)胞庫
種屬: 詳見細(xì)胞說明書組織: 詳見細(xì)胞說明書
細(xì)胞系: 詳見細(xì)胞說明書細(xì)胞形態(tài): 詳見細(xì)胞說明書
生長狀態(tài): 詳見細(xì)胞說明書靶點(diǎn): 詳見細(xì)胞說明書
應(yīng)用: 詳見細(xì)胞說明書貨號: 詳見細(xì)胞說明書
規(guī)格: 1*10^6cells/T25(1瓶)或1ml凍存管(2支)是否進(jìn)口: 來源ATCC、DSMZ、ECACC等細(xì)胞庫
組織來源: 詳見細(xì)胞說明書是否是腫瘤細(xì)胞: 詳見細(xì)胞說明書
器官來源: 詳見細(xì)胞說明書品系: 詳見細(xì)胞說明書
免疫類型: 詳見細(xì)胞說明書物種來源: 人源或其它動物來源等
保質(zhì)期: 可長期保存(液氮低溫凍存)
2025-02-07 AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 AsPC-1 1000000Cells/瓶/1RMB;2000000Cells/瓶/1RMB 1 ATCC、DSMZ等 美國、歐洲、德國等 低溫避光 AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 ATCC細(xì)胞庫

"AsPC-1人轉(zhuǎn)移胰腺腺癌細(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)

生長特性:貼壁生長

當(dāng)T25瓶復(fù)蘇細(xì)胞收到貨時,請觀察好細(xì)胞狀態(tài)后,將T25細(xì)胞瓶壁進(jìn)行75%酒精消毒,將T25瓶置于37度培養(yǎng)箱放置2-4h,以便穩(wěn)定細(xì)胞狀態(tài),當(dāng)細(xì)胞密度達(dá)80%-90%,即可進(jìn)行首次傳代培養(yǎng);干冰運(yùn)輸?shù)募?xì)胞凍存管收到貨后,需立即轉(zhuǎn)入液氮保存或直接進(jìn)行復(fù)蘇(第三天換液并檢查復(fù)蘇細(xì)胞密度,以便進(jìn)行下一步)。 能夠在實(shí)驗(yàn)室條件下進(jìn)行大量培養(yǎng)和繁殖。這種細(xì)胞系在分子生物學(xué)和生物技術(shù)研究中十分常用。

換液周期:每周2-3次

HPaSteC(HPSC) Cells;背景說明:胰腺星狀 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:C3H-10T1/2細(xì)胞、MyLa 2059細(xì)胞、HEL-92細(xì)胞

WM-239A Cells;背景說明:黑色素瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:KYSE 410細(xì)胞、BRL-3A細(xì)胞、Mel-624細(xì)胞

LMH Cells;背景說明:肝癌;雄性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SAOS 2細(xì)胞、Madin-Darby Canine Kidney細(xì)胞、NCI-H920細(xì)胞

AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息:該細(xì)胞來源于人胰腺癌裸鼠異種移植產(chǎn)生的癌性腹水,可以表達(dá)A,人胰腺相關(guān)抗原、人胰腺特異性抗原和黏蛋白。

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

DSMZ菌株保藏中心成立于1969年,是德國的國家菌種保藏中心。該中心一直致力于細(xì)菌、真菌、質(zhì)粒、抗菌素、人體和動物細(xì)胞、植物病毒等的分類、鑒定和保藏工作。DSMZ菌種保藏中心是歐洲規(guī)模最大的生物資源中心,保藏有動物細(xì)胞500多株。Riken BRC成立于1920年,是英國的國家菌種保藏中心。該中心一直致力于細(xì)菌、真菌、植物病毒等的分類、鑒定和保藏工作。日本Riken BRC(Riken生物資源保藏中心)是全球三大典型培養(yǎng)物收集中心之一。Riken保藏中心提供了很多細(xì)胞系。在世界范圍內(nèi),這些細(xì)胞系,都在醫(yī)學(xué)、科學(xué)和獸醫(yī)中具有重要意義。Riken生物資源中心支持了各種學(xué)術(shù)、健康、食品和獸醫(yī)機(jī)構(gòu)的研究工作,并在世界各地不同組織的微生物實(shí)驗(yàn)室和研究機(jī)構(gòu)中使用。

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)

來源說明:細(xì)胞主要來源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫

AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來源:人源、鼠源等其它物種來源

CL 1-0 Cells;背景說明:肺癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HFT-8810細(xì)胞、U373-MG細(xì)胞、NCI-H292細(xì)胞

Turbot Embryonic Cell line Cells;背景說明:胸腺;上皮 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:RAOEC細(xì)胞、SKNEP細(xì)胞、Caco-2/BBe細(xì)胞

GM03320D Cells;背景說明:該細(xì)胞是1967年4月由NicholsWW,LeeJ和DwightS建立,來源于一名13月齡白人男嬰腹部腫塊,臨床診斷為神經(jīng)母細(xì)胞瘤,伴有極少部位的類器官樣分化。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:存在兩種細(xì)胞類型,小的神經(jīng)母細(xì)胞樣細(xì)胞和大的透明成纖維樣細(xì)胞;相關(guān)產(chǎn)品有:TK.10細(xì)胞、HLEB3細(xì)胞、RH35細(xì)胞

526 mel Cells;背景說明:黑色素瘤;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:RTE細(xì)胞、293-EBNA細(xì)胞、Biologics Standards-Cercopithecus-1細(xì)胞

┈訂┈購(技術(shù)服務(wù))┈熱┈線:1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號】┈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)胞凍存復(fù)蘇材料與方法步驟:常用的細(xì)胞冷凍貯存器為貯存器,規(guī)格有35L和50L兩種。使用時要注意以下幾點(diǎn):(1)一般兩周需充一次,至少一個月充一次。溫度達(dá)-196℃,使用時注意勿讓濺到皮膚上,以免引起凍傷。(2)容器為雙層結(jié)構(gòu),中間為真空層,瓶口有雙層焊接處,應(yīng)防止焊接部裂開。(3)在裝入時,要注意緩慢小心,并用厚紙卷筒或制漏斗作引導(dǎo),使直達(dá)瓶底,如有專用灌注裝置則更HAO。若為初次使用,加時更要緩慢,以免溫度驟降而使容器損壞。細(xì)胞凍存時常備的材料有:0.25%胰蛋白酶,含10%~20%的血清培養(yǎng),DMSO(分析純)或無色新鮮甘油(121°C蒸氣GAO壓消毒),2mL安瓿(或?qū)S眉?xì)胞凍存管)、吸管、離心管、噴燈、紗布袋(或凍存管架)等。主要操作步驟為:(1)選擇處于對數(shù)生長期的細(xì)胞,在凍存前一天ZuiHAO換。將多個培養(yǎng)瓶中的細(xì)胞培養(yǎng) 去掉,用0.25%胰蛋白酶消化。適時去掉胰蛋白酶,加入少量新培養(yǎng)。用吸管吸取培養(yǎng)反復(fù)吹打瓶壁上的細(xì)胞,使其成為均勻分散的細(xì)胞懸。懸浮生產(chǎn)細(xì)胞則不要消化處理。然后將細(xì)胞收集于離心管中離心(1000r/min,10分鐘)。(2)去上清,加入含20%小牛血清的完全培養(yǎng)基,于4℃預(yù)冷15分鐘后,逐滴加入已無菌的DMSO或甘油,用吸管輕輕吹打使細(xì)胞均勻,細(xì)胞濃度為3×106~1×107/mL之間。(3)將上述細(xì)胞分裝于安瓿或?qū)S美鋬鏊芰瞎苤?,安瓿裝1~1.5mL在火焰噴燈上封口,封口處要完全封閉,圓滑無勾。冷凍管要將蓋子蓋緊,并標(biāo)記HAO細(xì)胞名稱和凍存日期,同時作HAO登記(日期、細(xì)胞種類及代次、凍存支數(shù))。(4)將裝HAO細(xì)胞的安瓿或凍存管裝入沙布袋內(nèi);置于容器頸口處存放過夜,次日轉(zhuǎn)入中。采用控制降溫速度的方法也可采用下列步驟:先將安瓿置入4℃冰箱中2~3小時,再移至冰箱冷凍室內(nèi)3~4小時,再吊入容器頸氣態(tài)部分存放2小時,Zui后沉入中。細(xì)胞凍存在中可以長期保存,但為妥善起見,凍存半年后,ZuiHAO取出一只安瓿細(xì)胞復(fù)蘇培養(yǎng),觀察生長情況,然后再繼續(xù)凍存。

CHL-IU Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:KU-812-F細(xì)胞、SK-BR3細(xì)胞、QGY-7703細(xì)胞

Centre Antoine Lacassagne-33 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Det. 562細(xì)胞、MV522細(xì)胞、MAC1細(xì)胞

H.Ep. #2 Cells;背景說明:最初認(rèn)為這個細(xì)胞源自喉上皮癌,但隨后通過同功酶分析、HeLa標(biāo)記染色體和DNA指紋分析發(fā)現(xiàn),起源細(xì)胞已被HeLa污染。 角蛋白免疫過氧化物酶染色陽性。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:H1792細(xì)胞、Hs 739.T細(xì)胞、COV-362細(xì)胞

Jiyoye (P-2003) Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每周2-3次。;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:H-1299細(xì)胞、COS1細(xì)胞、HMCB細(xì)胞

BOWES Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:6—1:10傳代,2天換液1次;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:T 24細(xì)胞、MDA 435細(xì)胞、3T3-A31細(xì)胞

Toledo Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每2-3天換液;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:G-361細(xì)胞、H-295細(xì)胞、KP4細(xì)胞

QBC939 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長 ;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HRA-19細(xì)胞、TE9細(xì)胞、C518細(xì)胞

LICR-HN6 Cells;背景說明:舌鱗癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NK10a細(xì)胞、MD Anderson-Metastatic Breast-468細(xì)胞、T-ALL 1細(xì)胞

MHCC 97 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:LL2細(xì)胞、EL-4細(xì)胞、MDA-kb2細(xì)胞

G 401 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:6傳代,每周2-3次。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:PC-9細(xì)胞、HO8910細(xì)胞、HEB細(xì)胞

PLMVEC Cells;背景說明:肺微血管;內(nèi)皮 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:JB6 clone 30, subclone 7b細(xì)胞、HTh-74細(xì)胞、L(TK-)細(xì)胞

NCI-H2108 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:COLO 684細(xì)胞、D6P2T細(xì)胞、University of Arizona Cell Culture-893細(xì)胞

MDA MB231 Cells;背景說明:MDA-MB-231來自患有轉(zhuǎn)移乳腺腺癌的51歲女病人的胸水。在裸鼠和ALS處理的BALB/c小鼠中,它能形成低分化腺癌(III級)。;傳代方法:消化3-5分鐘,1:2,3天內(nèi)可長滿;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:GS-9L細(xì)胞、T-ALL1細(xì)胞、KMST-6細(xì)胞

HECV Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:CCD 19Lu細(xì)胞、NCTC 3960細(xì)胞、PANC-28細(xì)胞

SUNE1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:GM06141B細(xì)胞、NCIH1930細(xì)胞、NCIH446細(xì)胞

DMS 79 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:4傳代;每周換液2-3次。;生長特性:懸浮生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SH-SY5Y Parental細(xì)胞、Cates-1B細(xì)胞、HN6細(xì)胞

Ramos 2G6.4C10 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法: 維持細(xì)胞濃度在2×105/ml-1×106/ml;根據(jù)細(xì)胞濃度每2-3天補(bǔ)液1次。;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:NSI/1-Ag4-1細(xì)胞、Hx147細(xì)胞、no.11細(xì)胞

Abcam HCT 116 EP300 KO Cells(提供STR鑒定圖譜)

AG06239 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSI556 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RST665 Cells(提供STR鑒定圖譜)

BIHi017-A Cells(提供STR鑒定圖譜)

Chula5.hES Cells(提供STR鑒定圖譜)

DA03187 Cells(提供STR鑒定圖譜)

DLD-1 clone A Cells(提供STR鑒定圖譜)

GM03037 Cells(提供STR鑒定圖譜)

P3HRI Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每2-3天換液;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:SCL I細(xì)胞、CCF-STTG1細(xì)胞、MDST8細(xì)胞

AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

SKBr3 Cells;背景說明:這株細(xì)胞源自胸水。沒有病毒顆粒。亞顯微結(jié)構(gòu)特征包括微絲和橋粒,肝糖原顆粒,大溶酶體,成束的細(xì)胞質(zhì)纖絲。SK-BR-3細(xì)胞株過表達(dá)HER2/c-erb-2基因產(chǎn)物。;傳代方法:消化3-5分鐘,1:2,3天內(nèi)可長滿;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:Hs-281-T細(xì)胞、HFTF細(xì)胞、OAW 42細(xì)胞

BE(2)C Cells;背景說明:神經(jīng)母細(xì)胞瘤;骨髓轉(zhuǎn)移;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SUM 149PT細(xì)胞、NT2/D1細(xì)胞、BALB/c 3T3 clone A31細(xì)胞

RGC-5 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:B16F0細(xì)胞、Human Epidermoid carcinoma #2細(xì)胞、A 72細(xì)胞

J 82 Cells;背景說明:電子顯微鏡下未觀察到橋粒但觀察到數(shù)目不同的粗面內(nèi)質(zhì)網(wǎng)和突出微絲。 含ras (H-ras)癌基因。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:RK-13細(xì)胞、MNNG-HOS (TE 85, clone F-5)細(xì)胞、REC細(xì)胞

PLC-PRF-5 Cells;背景說明:該細(xì)胞系分泌乙肝病毒表面抗原(HBsAg)。 此細(xì)胞系原先被支原體污染,后用BM-cycline去除支原體;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:NCIH345細(xì)胞、DU 4475細(xì)胞、207細(xì)胞

56.4H7 Cells(提供STR鑒定圖譜)

YES2 Cells;背景說明:食管鱗癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MDAMB175細(xì)胞、WM2664細(xì)胞、H-295R細(xì)胞

Malme-3 M Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:4傳代,2天換液1次。;生長特性:混合生長;形態(tài)特性:成纖維細(xì)胞;相關(guān)產(chǎn)品有:KNS-62細(xì)胞、NS1-Ag 4/1細(xì)胞、SRS-82細(xì)胞

Adeno 293 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:COLO-824細(xì)胞、Hep-G2/C3A細(xì)胞、HCAEC細(xì)胞

A 172 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:A427細(xì)胞、BEAS2B細(xì)胞、Tissue Culture-1細(xì)胞

CSQT-2 Cells;背景說明:肝癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Blotchy fibroblast-11細(xì)胞、COR-L88細(xì)胞、BT-474細(xì)胞

H1650 Cells;背景說明:該細(xì)胞是從一名27歲白人男性(10年煙齡)支氣管肺泡癌患者的胸腔積液中分離得到的。;傳代方法:1:4-1:6傳代;2-3天換液1次。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:H2171細(xì)胞、PLB-985細(xì)胞、HCCLM6細(xì)胞

H1650 Cells;背景說明:該細(xì)胞是從一名27歲白人男性(10年煙齡)支氣管肺泡癌患者的胸腔積液中分離得到的。;傳代方法:1:4-1:6傳代;2-3天換液1次。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:H2171細(xì)胞、PLB-985細(xì)胞、HCCLM6細(xì)胞

MCF 7B Cells;背景說明:浸潤性導(dǎo)管癌;胸腔積液轉(zhuǎn)移;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:J-111細(xì)胞、CCD 1112SK細(xì)胞、Hep 2細(xì)胞

GM20891 Cells(提供STR鑒定圖譜)

HAP1 KIF15 (-) 1 Cells(提供STR鑒定圖譜)

SK-RC-20 Cells;背景說明:腎癌;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:CT 26細(xì)胞、L 1210細(xì)胞、TE 32.T細(xì)胞

HCC-1833 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Menschliche Und Tierische Zellkulture-1細(xì)胞、Panc 5.04細(xì)胞、HOCF細(xì)胞

BpRcl Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4-1:6傳代;每周換液2-3次。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:HTR-8/SV neo細(xì)胞、NCI-H508細(xì)胞、ARH 77細(xì)胞

OCI-AML4 Cells;背景說明:急性髓系白血??;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HCC-94細(xì)胞、F36P細(xì)胞、Colo320細(xì)胞

373 MG Cells;背景說明:膠質(zhì)瘤;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:OEC19細(xì)胞、MAVER1細(xì)胞、NCIH295R細(xì)胞

H2452 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:消化3-5分鐘。1:2。3天內(nèi)可長滿。;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:BrCL12細(xì)胞、PTK2細(xì)胞、EB2細(xì)胞

RA 1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NCTC 1469細(xì)胞、A549 ATCC細(xì)胞、A-704細(xì)胞

H.Ep.-2 Cells;背景說明:最初認(rèn)為這個細(xì)胞源自喉上皮癌,但隨后通過同功酶分析、HeLa標(biāo)記染色體和DNA指紋分析發(fā)現(xiàn),起源細(xì)胞已被HeLa污染。 角蛋白免疫過氧化物酶染色陽性。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:SNU-886細(xì)胞、PLA802細(xì)胞、BT-B細(xì)胞

HPS2973 Cells(提供STR鑒定圖譜)

Jurkat-JMN Cells(提供STR鑒定圖譜)

mDD1 Cells(提供STR鑒定圖譜)

NEYS Cells(提供STR鑒定圖譜)

PUMCHi001-A Cells(提供STR鑒定圖譜)

Ubigene HCT 116 CHD8 KO Cells(提供STR鑒定圖譜)

VRISGi004-A Cells(提供STR鑒定圖譜)

HCT116-SN6 Cells(提供STR鑒定圖譜)

GA-10 clone 4 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每2-3天換液;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:P388.D1細(xì)胞、Hs 636 T細(xì)胞、SNU-869細(xì)胞

HEC-1-A Cells;背景說明:這株細(xì)胞及其亞株HEC-1-B是H.Kuramoto及其同事1968年從一位IA期子宮內(nèi)膜癌患者身上分離得到的。PAF可以誘導(dǎo)其c-fos的表達(dá)。;傳代方法:消化3-5分鐘,1:2,3天內(nèi)可長滿;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:WSU-DLCL2細(xì)胞、U-87 MG細(xì)胞、Ramos.2G6.4C10細(xì)胞

mRMEC Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:A375mel細(xì)胞、SCL-II細(xì)胞、SK-GT-2細(xì)胞

SNU-886 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SuDHL 2細(xì)胞、RBL 1細(xì)胞、MIN-6細(xì)胞

NOZC-1 Cells;背景說明:患者有癌性腹膜炎。細(xì)胞為中等分化的管狀膽囊癌。會分泌AFP和CEA。倍增時間48小時,板植率14-19%。細(xì)胞可在裸鼠中成瘤,形態(tài)與原發(fā)腫瘤相似。;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:F442A細(xì)胞、MFE-280細(xì)胞、Hs 636.T細(xì)胞

K562/ADR Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:LCMS細(xì)胞、PG-4細(xì)胞、HSC-I細(xì)胞

Rat Fetal Lung-6 Cells;背景說明:胚肺;成纖維細(xì)胞;SD大鼠;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:JB6 [Mouse]細(xì)胞、HUV-EC-C細(xì)胞、SK-MEL-2細(xì)胞

H4-II-EC3 Cells;背景說明:在糖皮質(zhì)激素、胰島素或cAMP衍生物的誘導(dǎo)下可以產(chǎn)生酪酸基轉(zhuǎn)移酶;可被逆轉(zhuǎn)錄病毒感染;可產(chǎn)生白蛋白、轉(zhuǎn)鐵蛋白、凝血酶原;在AxC大鼠中可以成瘤。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:SUM-190細(xì)胞、SKRC-20細(xì)胞、T241細(xì)胞

OEC33 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:ZR-75-1細(xì)胞、HPF細(xì)胞、Wien133細(xì)胞

Mv 1 Lu Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Sf-21細(xì)胞、C4-1細(xì)胞、RL-65細(xì)胞

Jurkat E6-1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:CLL-CII細(xì)胞、Colon-26細(xì)胞、HB 611細(xì)胞

Karpas-422 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Colon 38細(xì)胞、T.T細(xì)胞、Caco-2/ATCC細(xì)胞

EM-3 Cells;背景說明:髓系白血??;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:WERI-Rb-1細(xì)胞、SUP T1細(xì)胞、CNE-2細(xì)胞

L 132 Cells;背景說明:胚肺;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Roswell Park Memorial Institute 8226細(xì)胞、MES-13細(xì)胞、H1694細(xì)胞

MPP 89 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:KY180細(xì)胞、Sp 2/0-Ag 14細(xì)胞、INS1細(xì)胞

SNUhES46 Cells(提供STR鑒定圖譜)

7860 Cells;背景說明:該細(xì)胞源自一位原發(fā)性腎透明細(xì)胞癌患者。該細(xì)胞有微絨毛和橋粒,能在軟瓊脂上生長。此細(xì)胞生成一種PTH(甲狀旁腺素)樣的多肽,與乳癌和肺癌中生成的肽相似,其N端序列與PTH相似,具有PTH樣活性,分子量為6000D。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:HPAF II細(xì)胞、IMR90細(xì)胞、RS411細(xì)胞

HIMEC Cells;背景說明:腸微血管內(nèi)皮 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NCI-157細(xì)胞、2V6.11細(xì)胞、SCL-2細(xì)胞

LM3 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:HCC1500細(xì)胞、UCLA-SO-M14細(xì)胞、H-35細(xì)胞

MT-2 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:Stanford University-Diffuse Histiocytic Lymphoma-16細(xì)胞、SKNO-1細(xì)胞、RPTEC TERT1細(xì)胞

MV-522 Cells;背景說明:肺腺癌;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SUM 102細(xì)胞、451-LU細(xì)胞、Caki2細(xì)胞

Walker 256 Cells;背景說明:乳腺癌;雌性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Centre Antoine Lacassagne-85-1細(xì)胞、GBC-SD細(xì)胞、BHP 10-3細(xì)胞

AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

Panc 4.03 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:WEHI-3細(xì)胞、RTE細(xì)胞、NCI-H2452細(xì)胞

SNUC1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每3-5天換液。;生長特性:懸浮生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:HSC3細(xì)胞、PY8119細(xì)胞、AML-EOL-1細(xì)胞

CEM-0 Cells;背景說明:G.E. Foley 等人建立了類淋巴母細(xì)胞細(xì)胞株CCRF-CEM。 細(xì)胞是1964年11月從一位四歲白人女性急性淋巴細(xì)胞白血病患者的外周血白血球衣中得到。此細(xì)胞系從香港收集而來。;傳代方法:1:2傳代。3天內(nèi)可長滿。;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:33604細(xì)胞、NCIH1341細(xì)胞、NB1-RGB細(xì)胞

3T3 L1 Cells;背景說明:3T3-L1是從3T3細(xì)胞(Swissalbino)中經(jīng)克隆分離得到的連續(xù)傳代的亞系。該細(xì)胞從快速分裂到匯合和接觸性抑制狀態(tài)經(jīng)歷了前脂肪細(xì)胞到脂肪樣細(xì)胞的轉(zhuǎn)變。該細(xì)胞鼠痘病毒陰性;可產(chǎn)生甘油三酯,高濃度血清可增強(qiáng)細(xì)胞內(nèi)脂肪堆積。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:NL20SV細(xì)胞、2008細(xì)胞、H2286細(xì)胞

NG-108-15 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:TC-1 [Mouse lung]細(xì)胞、CAL62細(xì)胞、Primary Liver Carcinoma/Poliomyelitis Research Foundation/5細(xì)胞

SKM1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;;生長特性:貼壁生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:QBC-939細(xì)胞、LS-411N細(xì)胞、L-6 myoblast細(xì)胞

CAL 148 Cells;背景說明:乳腺癌;胸腔積液轉(zhuǎn)移;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HCT GEO細(xì)胞、Detroit-562細(xì)胞、SaOS細(xì)胞

Huh7.5 Cells;背景說明:肝癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Simpson細(xì)胞、Vx-2細(xì)胞、HSF細(xì)胞

BayGenomics ES cell line RRK260 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XL978 Cells(提供STR鑒定圖譜)

GLUTag Cells(提供STR鑒定圖譜)

OLF10.1.8 Cells(提供STR鑒定圖譜)

1.1B4 Cells(提供STR鑒定圖譜)

MCW073i-40000527 Cells(提供STR鑒定圖譜)

" "PubMed=1764370; DOI=10.1038/bjc.1991.467; PMCID=PMC1977874

Barton C.M., Staddon S.L., Hughes C.M., Hall P.A., O'Sullivan C., Kloppel G., Theis B., Russell R.C.G., Neoptolemos J., Williamson R.C.N., Lane D.P., Lemoine N.R.

Abnormalities of the p53 tumour suppressor gene in human pancreatic cancer.

Br. J. Cancer 64:1076-1082(1991)


PubMed=1630814

Ruggeri B.A., Zhang S.-Y., Caamano J., DiRado M., Flynn S.D., Klein-Szanto A.J.P.

Human pancreatic carcinomas and cell lines reveal frequent and multiple alterations in the p53 and Rb-1 tumor-suppressor genes.

Oncogene 7:1503-1511(1992)


PubMed=7972006; DOI=10.1073/pnas.91.23.11045; PMCID=PMC45163

Okamoto A., Demetrick D.J., Spillare E.A., Hagiwara K., Hussain S.P., Bennett W.P., Forrester K., Gerwin B.I., Serrano M., Beach D.H., Harris C.C.

Mutations and altered expression of p16INK4 in human cancer.

Proc. Natl. Acad. Sci. U.S.A. 91:11045-11049(1994)


PubMed=8026879; DOI=10.1002/ijc.2910580207

Berrozpe G., Schaeffer J., Peinado M.A., Real F.X., Perucho M.

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

Int. J. Cancer 58:185-191(1994)


PubMed=8194712; DOI=10.1016/0016-5085(94)90422-7

Simon B., Weinel R., Hohne M., Watz J., Schmidt J., Kortner G., Arnold R.

Frequent alterations of the tumor suppressor genes p53 and DCC in human pancreatic carcinoma.

Gastroenterology 106:1645-1651(1994)


PubMed=8286197; DOI=10.1038/bjc.1994.24; PMCID=PMC1968784

Lohr J.-M., Trautmann B., Gottler M., Peters S., Zauner I., Maillet B., Kloppel G.

Human ductal adenocarcinomas of the pancreas express extracellular matrix proteins.

Br. J. Cancer 69:144-151(1994)


PubMed=21607521; DOI=10.3892/or.1.6.1223

Iguchi H., Morita R., Yasuda D., Takayanagi R., Ikeda Y., Takada Y., Shimazoe T., Nawata H., Kono A.

Alterations of the p53 tumor-suppressor gene and ki-ras oncogene in human pancreatic cancer-derived cell-lines with different metastatic potential.

Oncol. Rep. 1:1223-1227(1994)


PubMed=9331070

Teng D.H.-F., Perry W.L. 3rd, Hogan J.K., Baumgard M.L., Bell R., Berry S., Davis T., Frank D., Frye C., Hattier T., Hu R., Jammulapati S., Janecki T., Leavitt A., Mitchell J.T., Pero R., Sexton D., Schroeder M., Su P.-H., Swedlund B., Kyriakis J.M., Avruch J., Bartel P., Wong A.K.C., Oliphant A., Thomas A., Skolnick M.H., Tavtigian S.V.

Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor.

Cancer Res. 57:4177-4182(1997)


PubMed=9665481; DOI=10.1016/S0002-9440(10)65561-7; PMCID=PMC1852940

Paciucci R., Vila M.R., Adell T., Diaz V.M., Tora M., Nakamura T., Real F.X.

Activation of the urokinase plasminogen activator/urokinase plasminogen activator receptor system and redistribution of E-cadherin are associated with hepatocyte growth factor-induced motility of pancreas tumor cells overexpressing Met.

Am. J. Pathol. 153:201-212(1998)


PubMed=10027410; DOI=10.1016/S0002-9440(10)65298-4; PMCID=PMC1850008

Ghadimi B.M., Schrock E., Walker R.L., Wangsa D., Jauho A., Meltzer P.S., Ried T.

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

Am. J. Pathol. 154:525-536(1999)


PubMed=10408907; DOI=10.1016/S0304-3835(98)00380-2

Bartsch D.K., Barth P., Bastian D., Ramaswamy A., Gerdes B., Chaloupka B., Deiss Y., Simon B., Schudy A.

Higher frequency of DPC4/Smad4 alterations in pancreatic cancer cell lines than in primary pancreatic adenocarcinomas.

Cancer Lett. 139:43-49(1999)


PubMed=11115575; DOI=10.3892/or.8.1.89

Sun C.-L., Yamato T., Furukawa T., Ohnishi Y., Kijima H., Horii A.

Characterization of the mutations of the K-ras, p53, p16, and SMAD4 genes in 15 human pancreatic cancer cell lines.

Oncol. Rep. 8:89-92(2001)


PubMed=11169959; DOI=10.1002/1097-0215(200002)9999:9999<::AID-IJC1049>3.0.CO;2-C

Sirivatanauksorn V., Sirivatanauksorn Y., Gorman P.A., Davidson J.M., Sheer D., Moore P.S., Scarpa A., Edwards P.A.W., Lemoine N.R.

Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.

Int. J. Cancer 91:350-358(2001)


PubMed=11787853; DOI=10.1007/s004280100474

Moore P.S., Sipos B., Orlandini S., Sorio C., Real F.X., Lemoine N.R., Gress T.M., Bassi C., Kloppel G., Kalthoff H., Ungefroren H., Lohr J.-M., Scarpa A.

Genetic profile of 22 pancreatic carcinoma cell lines. Analysis of K-ras, p53, p16 and DPC4/Smad4.

Virchows Arch. 439:798-802(2001)


PubMed=12692724; DOI=10.1007/s00428-003-0784-4

Sipos B., Moser S., Kalthoff H., Torok V., Lohr J.-M., Kloppel G.

A comprehensive characterization of pancreatic ductal carcinoma cell lines: towards the establishment of an in vitro research platform.

Virchows Arch. 442:444-452(2003)


PubMed=14695172

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=16912165; DOI=10.1158/0008-5472.CAN-06-0721

Calhoun E.S., Hucl T., Gallmeier E., West K.M., Arking D.E., Maitra A., Iacobuzio-Donahue C.A., Chakravarti A., Hruban R.H., Kern S.E.

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.

Cancer Res. 66:7920-7928(2006)


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)


DOI=10.4172/2324-9293.1000104

Wagenhauser M.U., Ruckert F., Niedergethmann M., Grutzmann R., Saeger H.-D.

Distribution of characteristic mutations in native ductal adenocarcinoma of the pancreas and pancreatic cancer cell lines.

Cell Biol. Res. Ther. 2:1000104.1-1000104.5(2013)


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=25984343; DOI=10.1038/sdata.2014.35; PMCID=PMC4432652

Cowley G.S., Weir B.A., Vazquez F., Tamayo P., Scott J.A., Rusin S., East-Seletsky A., Ali L.D., Gerath W.F.J., Pantel S.E., Lizotte P.H., Jiang G.-Z., Hsiao J., Tsherniak A., Dwinell E., Aoyama S., Okamoto M., Harrington W., Gelfand E.T., Green T.M., Tomko M.J., Gopal S., Wong T.C., Li H.-B., Howell S., Stransky N., Liefeld T., Jang D., Bistline J., Meyers B.H., Armstrong S.A., Anderson K.C., Stegmaier K., Reich M., Pellman D., Boehm J.S., Mesirov J.P., Golub T.R., Root D.E., Hahn W.C.

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Sci. Data 1:140035-140035(2014)


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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.

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


PubMed=25877200; DOI=10.1038/nature14397

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

Nature 520:307-311(2015)


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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)


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Tumor Biol. 37:5847-5855(2016)


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.

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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.

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關(guān)鍵字: AsPC-1人轉(zhuǎn)移胰腺腺癌細(xì)胞代次低|培;復(fù)蘇細(xì)胞系;細(xì)胞STR鑒定報告;細(xì)胞STR鑒定圖譜;ATCC|DSMZ細(xì)胞庫;

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公司提供ATCC、DSMZ、ECACC、NCI-DTP、RCB(Riken)等細(xì)胞系
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主營行業(yè) 細(xì)胞培養(yǎng),細(xì)胞生物學(xué),生物技術(shù)服務(wù) 經(jīng)營模式 貿(mào)易,工廠,服務(wù)
  • 上海賓穗生物科技有限公司
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  • 公司成立:8年
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  • 主營產(chǎn)品:ATCC細(xì)胞、DSMZ細(xì)胞系、ECACC細(xì)胞系
  • 公司地址:手機(jī)號/微信號:13641930791 上海市紫竹科學(xué)園區(qū)
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