成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書,AsPC-1
  • AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書,AsPC-1

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

價(jià)格 詢價(jià)
包裝 1000000細(xì)胞數(shù) 2000000細(xì)胞數(shù)
最小起訂量 1000000細(xì)胞數(shù)
發(fā)貨地 上海
更新日期 2025-02-23
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書英文名稱:AsPC-1
品牌: ATCC\RCB等產(chǎn)地: 國外
保存條件: 常溫培養(yǎng)或液氮凍存純度規(guī)格: AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書
產(chǎn)品類別: 化學(xué)試劑
種屬: 詳見產(chǎn)品資料組織: 詳見產(chǎn)品資料
細(xì)胞系: 詳見產(chǎn)品資料細(xì)胞形態(tài): 詳見產(chǎn)品資料
生長狀態(tài): 詳見產(chǎn)品資料靶點(diǎn): 詳見產(chǎn)品資料
應(yīng)用: 詳見產(chǎn)品資料
2025-02-23 AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書 AsPC-1 1000000細(xì)胞數(shù)/RMB;2000000細(xì)胞數(shù)/RMB ATCC\RCB等 國外 常溫培養(yǎng)或液氮凍存 AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書 化學(xué)試劑

"AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

傳代比例:1:2-1:4(首次傳代建議1:2)

生長特性:貼壁生長

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(shí)要注意以下幾點(diǎn):(1)一般兩周需充一次,至少一個(gè)月充一次。溫度達(dá)-196℃,使用時(shí)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(shí),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(shí)更要緩慢,以免溫度驟降而使容器損壞。細(xì)胞凍存時(shí)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(duì)數(shù)生長期的細(xì)胞,在凍存前一天ZuiHAO換。將多個(gè)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(shí)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(shí)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(shí),再移至冰箱冷凍室內(nèi)3~4小時(shí),再吊入容器頸氣態(tài)部分存放2小時(shí),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。

換液周期:每周2-3次

MCA 38 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:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:MeSoTheliOma-211H細(xì)胞、NSI/1-Ag4-1細(xì)胞、GC-1spg細(xì)胞

U-87MG ATCC 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:BJ [Human fibroblast]細(xì)胞、SW 1222細(xì)胞、HT-1376細(xì)胞

ML-2 Cells;背景說明:急性髓單核細(xì)胞白血??;男性;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:CAMA細(xì)胞、H2452細(xì)胞、NCIH508細(xì)胞

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

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。

公司細(xì)胞系形態(tài)漂亮、增殖倍數(shù)高、純度高、功能性強(qiáng),細(xì)胞培養(yǎng)就跟養(yǎng)孩子一個(gè)樣。養(yǎng)孩子要喂奶,養(yǎng)細(xì)胞要加補(bǔ)液,都需要在前期補(bǔ)充足夠的營養(yǎng),初始狀態(tài)的細(xì)胞或剛剛復(fù)蘇的細(xì)胞還要適量加入血清或細(xì)胞因子來幫助它們的存活增殖,如果營養(yǎng)物質(zhì)缺乏,細(xì)胞就會(huì)不生長甚至死亡。養(yǎng)孩子要從小培養(yǎng)學(xué)習(xí),養(yǎng)細(xì)胞也得培養(yǎng)寶寶順利生下來,你會(huì)經(jīng)常撫摸他,給他看各種顏色,刺激他的五感。細(xì)胞也是一樣,分離后的細(xì)胞需要使用特定的細(xì)胞因子進(jìn)行活化、增殖。另外加入因子的種類、因子的濃度、加入時(shí)間、加入順序都會(huì)影響細(xì)胞最終的結(jié)果。養(yǎng)孩子最怕孩子生病,養(yǎng)細(xì)胞最怕被污染,平時(shí)你會(huì)仔細(xì)觀察寶寶是否嘔吐、是否突然哭鬧,猜測(cè)寶寶是否生病了。對(duì)于細(xì)胞,我們也需要時(shí)刻進(jìn)行觀察的,假如培養(yǎng)液渾濁(污染了),則需要換液后加抗生素;假如細(xì)胞增殖不明顯,形態(tài)變差,則可能是因?yàn)闋I養(yǎng)不足了,對(duì)貼壁細(xì)胞可以消化后重新用新的培養(yǎng)基接種并加倍加入細(xì)胞因子含量;對(duì)懸浮細(xì)胞增殖能力不強(qiáng)的,則不著急補(bǔ)液,只是先補(bǔ)加血清、細(xì)胞因子看是否可以好轉(zhuǎn)。培養(yǎng)時(shí)還得全程在無菌的環(huán)境,一個(gè)小小的偏差,細(xì)胞就會(huì)死亡。

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

CEMC7 Cells;背景說明:急性T淋巴細(xì)胞白血?。慌?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:HPDLF細(xì)胞、Jijoye細(xì)胞、H.Ep. #2細(xì)胞

U 138 MG Cells;背景說明:星形細(xì)胞瘤;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:A375-MEL細(xì)胞、R-1059-D細(xì)胞、32D-Cl3細(xì)胞

NCI-HUT-520 Cells;背景說明:詳見相關(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:P3J HR-1細(xì)胞、RS(4;11)細(xì)胞、MF2059細(xì)胞

Pro-5 Lec1.3c 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:HuH28細(xì)胞、VM Cub 1細(xì)胞、HS-294T細(xì)胞

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

物種來源:人源、鼠源等其它物種來源

形態(tài)特性:上皮細(xì)胞樣

細(xì)胞凍存知識(shí)普及:細(xì)胞凍存是細(xì)胞保存的主要方法之一。利用凍存技術(shù)將細(xì)胞置于-196℃中低溫保存,可以使細(xì)胞暫時(shí)脫離生長狀態(tài)而將其細(xì)胞性保存起來,這樣在需要的時(shí)候再復(fù)蘇細(xì)胞用于實(shí)驗(yàn)。而且適度地保存一定量的細(xì)胞,可以防止因正在培養(yǎng)的細(xì)胞被污染或其他意外事件而使細(xì)胞丟種,起到了細(xì)胞保種的作用。除此之外,還可以利用細(xì)胞凍存的形式來購買、寄贈(zèng)、交換和運(yùn)送某些細(xì)胞。細(xì)胞凍存時(shí)向培養(yǎng)基中加入保護(hù)劑--終濃度5%.15%的甘油或二甲基亞砜(DMSO),可使溶冰點(diǎn)降低,加之在緩慢凍結(jié)條件下,細(xì)胞內(nèi)水分透出,減少了冰晶形成,從而避免細(xì)胞損傷。 采用""慢凍快融""的方法能較HAO地保證細(xì)胞存活。標(biāo)準(zhǔn)冷凍速度開始為-1到-2℃/min,當(dāng)溫度低于-25℃時(shí)可加速,到-80℃之后可直接投入內(nèi)(-196℃)。

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

ARO81 Cells;背景說明:甲狀腺癌;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:SN12C細(xì)胞、Y3-Ag1,2,3細(xì)胞、Baby Hamster Kidney from litter No. 21細(xì)胞

hFOB1.19 Cells;背景說明:成骨細(xì)胞;SV40轉(zhuǎn)化;條件永生;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:Helacyton gartleri細(xì)胞、IPLB-SF 21細(xì)胞、Ramos細(xì)胞

SUM-159 Cells;背景說明:乳腺癌;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:NCI-H1341細(xì)胞、HS5細(xì)胞、JurkatE6-1細(xì)胞

SUP-T1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:2-3天換液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:N-2a細(xì)胞、A-431細(xì)胞、SN12C細(xì)胞

H209 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次。;生長特性:懸浮生長,有少數(shù)細(xì)胞疏松貼壁;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:HN6細(xì)胞、SKHEP1細(xì)胞、SPCA1細(xì)胞

C32 mel 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:貼壁生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MESSA-DX5細(xì)胞、C1R細(xì)胞、NGEC細(xì)胞

SUM 52 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:MDA415細(xì)胞、SU86-86細(xì)胞、SKRC-20細(xì)胞

Wien133 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:CHL-CL-11細(xì)胞、BALL1細(xì)胞、LTEP-a2細(xì)胞

Panc8.13 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:GM04680細(xì)胞、Nb2a細(xì)胞、NCIH660細(xì)胞

MDCC-MSB1 Cells;背景說明:淋巴瘤;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:GA10細(xì)胞、CHO Lec1細(xì)胞、KE-37細(xì)胞

NRK Cells;背景說明:腎;自發(fā)永生;Osborne-Mendel;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:DC2.4細(xì)胞、Sp2/O-Ag14細(xì)胞、NCTC-3960細(xì)胞

CCRF-CEM C7 Cells;背景說明:急性T淋巴細(xì)胞白血??;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:1301細(xì)胞、Colon 26細(xì)胞、Alexander細(xì)胞

BT-325 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:SNU601細(xì)胞、Merwin Plasma Cell tumor-11細(xì)胞、NCI-H87細(xì)胞

NCI-H1793 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:6傳代 ;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:Sol8細(xì)胞、Colo-678細(xì)胞、H-2135細(xì)胞

GM03570E 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:SU-DHL-2細(xì)胞、WM-239A細(xì)胞、Lu-165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

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

371M Cells(提供STR鑒定圖譜)

Abcam HeLa VOPP1 KO Cells(提供STR鑒定圖譜)

AIW002-02/MAPT-KO Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRJ292 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XK248 Cells(提供STR鑒定圖譜)

C6-Russian Cells(提供STR鑒定圖譜)

DA00311 Cells(提供STR鑒定圖譜)

FLAM-76 Cells(提供STR鑒定圖譜)

GM09382 Cells(提供STR鑒定圖譜)

OCI-Ly1 Cells;背景說明:彌漫大B淋巴瘤;男性;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:THPI細(xì)胞、Mahlavu細(xì)胞、HCC1500細(xì)胞

293/EBNA Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4-1:10傳代;每周2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:LS-180細(xì)胞、Line 870 Emory University-4細(xì)胞、MC3T3, E1 subgroup-4 clone細(xì)胞

GM3569 Cells;背景說明:該細(xì)胞是由綿羊紅細(xì)胞免疫的BALB/c小鼠脾細(xì)胞和P3X63Ag8骨髓瘤細(xì)胞融合得到的。該細(xì)胞不分泌免疫球蛋白,對(duì)20μg/ml的8-氮鳥嘌呤有抗性,對(duì)HAT比較敏感;該細(xì)胞可以作為細(xì)胞融合時(shí)的B細(xì)胞組分用于制備雜交瘤;鼠痘病毒陰性。;傳代方法:1:2傳代;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞樣;圓形;相關(guān)產(chǎn)品有:P3.NS-1/1.Ag4.1細(xì)胞、MDA-MB361細(xì)胞、KNS-81細(xì)胞

SNUC2B 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:PaTu 8988 S細(xì)胞、H-727細(xì)胞、C-28/I2細(xì)胞

T-84 Cells;背景說明:T84細(xì)胞株是從一位72歲男性結(jié)腸癌患者的肺轉(zhuǎn)移灶建立的可移植人類癌細(xì)胞株。 腫瘤組織皮下接種于BALB/c裸鼠,并連續(xù)進(jìn)行移植。 [26072] 在裸鼠身上的移植過程中,細(xì)胞株始終保持結(jié)腸癌的原始組織性狀。 [26072] 在無胸腺小鼠中傳代23代后建立了T84細(xì)胞株。 這些細(xì)胞單層生長到飽和并在接觸細(xì)胞間展現(xiàn)出緊密連接和橋粒。 [1155] 有很多關(guān)于多肽類激素和神經(jīng)遞質(zhì)并維持定向電解質(zhì)傳輸?shù)氖荏w。 [1155] 這株細(xì)胞展現(xiàn)了接觸細(xì)胞中的緊密連接和橋粒。 [1155] 角蛋白免疫過氧化物酶染色陽性。;傳代方法:1:2-1:4傳代;每周2次。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞,多角;相關(guān)產(chǎn)品有:SK-RC 39細(xì)胞、HCC1500細(xì)胞、BHP10-3細(xì)胞

Rat 2 Cells;背景說明:成纖維細(xì)胞;自發(fā)永生;Fischer 344;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:AR4IP細(xì)胞、TEV-1細(xì)胞、253J B-V細(xì)胞

BayGenomics ES cell line BGC030 Cells(提供STR鑒定圖譜)

SNU251 Cells;背景說明:卵巢內(nèi)膜癌;腹水轉(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:LS 513細(xì)胞、L-Wnt-3A細(xì)胞、AN3-CA細(xì)胞

NUGC3 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:6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:VMRC-RCZ細(xì)胞、SU-DHL6細(xì)胞、16-HBEo細(xì)胞

MDCK-2 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3傳代,3-4天傳1次;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:Ku812F細(xì)胞、HS578T細(xì)胞、Swiss/3T3細(xì)胞

Virginia Mason Research Center-Lung Cancer D 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:H211細(xì)胞、CLL-CII細(xì)胞、bEnd.3[BEND3]細(xì)胞

MILE SVEN 1 Cells;背景說明:MS1是1994年建株的胰島內(nèi)皮細(xì)胞株。原代培養(yǎng)的胰島內(nèi)皮細(xì)胞用抗G418的溫度敏感型SV40大T抗原(tsA-58-3)轉(zhuǎn)染??剐钥寺∮每寺…h(huán)分離,并篩選吸收dil-Ac-LDL的。這株細(xì)胞保留了內(nèi)皮細(xì)胞的許多特性,如吸收乙酰化LDL和表達(dá)八因子相關(guān)抗原及BEGF受體。;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:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:AN3 CA細(xì)胞、Ha Fe細(xì)胞、GM04154細(xì)胞

HNE1 Cells;背景說明:鼻咽部;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:RINm5F細(xì)胞、TE-14細(xì)胞、AX-Mel細(xì)胞

KU-812 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;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:骨髓母細(xì)胞;相關(guān)產(chǎn)品有:PC14細(xì)胞、2008細(xì)胞、NKT細(xì)胞

Panc-327 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:HCEC-12細(xì)胞、SN12C細(xì)胞、SNU-C2B細(xì)胞

GM13696 Cells(提供STR鑒定圖譜)

HAP1 FUT8 (-) 3 Cells(提供STR鑒定圖譜)

RPMI 7951 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:貼壁生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:X63.Ag8.653細(xì)胞、BEAS 2B細(xì)胞、SU-DHL-4細(xì)胞

Hs27F Cells;背景說明:包皮;成纖維細(xì)胞;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:LWnt3A細(xì)胞、IPLB-Sf21-AE細(xì)胞、HLEpiC細(xì)胞

VeroC1008 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:Bronchial Epithelium transformed with Ad12-SV40 2B細(xì)胞、CEMO-1細(xì)胞、EST81細(xì)胞

MDAMB231 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(jí))。;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:MUTZ-1細(xì)胞、PANC-08-13細(xì)胞、H128細(xì)胞

RCM-1 [Human rectum adenocarcinoma] Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4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;相關(guān)產(chǎn)品有:HPDE細(xì)胞、TOV-21G細(xì)胞、H-2107細(xì)胞

JHH-2 Cells;背景說明:肝癌;腹水轉(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:MRC-9細(xì)胞、LP1細(xì)胞、IM95細(xì)胞

HCC-1806 Cells;背景說明:該細(xì)胞源自一位患有乳腺髓樣癌的44歲黑人女性,表達(dá)WNT7B癌基因,細(xì)胞與細(xì)胞邊界處有細(xì)胞橋粒、微絨毛、張力細(xì)絲。;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:D324 Med細(xì)胞、RBL 2H3細(xì)胞、HCS2/8細(xì)胞

SN4741 Cells;背景說明:多巴胺能神經(jīng) 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:Tb1.Lu細(xì)胞、Tn-5細(xì)胞、Fetal Human Lens-124細(xì)胞

HMMMF Cells(提供STR鑒定圖譜)

ISt-1 Cells(提供STR鑒定圖譜)

MCF-7GFP Cells(提供STR鑒定圖譜)

ND13698 Cells(提供STR鑒定圖譜)

PPMI.I.1065.1 Cells(提供STR鑒定圖譜)

UCSD225i-NDC1-3 Cells(提供STR鑒定圖譜)

ZZUi030-A Cells(提供STR鑒定圖譜)

HCT116-SLC22A23-KO-c7 Cells(提供STR鑒定圖譜)

H716 Cells;背景說明:從一位經(jīng)5-尿嘧啶治療的患者腹水中得到的細(xì)胞建立了這個(gè)細(xì)胞株。 與其它結(jié)直腸癌細(xì)胞系不同,這株細(xì)胞有多巴脫羧酶,細(xì)胞質(zhì)中有核心致密的內(nèi)分泌型顆粒。 這株細(xì)胞不表達(dá)TAG-72 或CA19-9抗原,也不生成癌胚抗原(CEA);傳代方法:1:3—1:6傳代,每周換液2—3次;生長特性:懸浮生長,聚團(tuán),少數(shù)貼壁;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:Colo16細(xì)胞、BRL 3A細(xì)胞、NCI-H1666細(xì)胞

PTK2 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:JIII細(xì)胞、OVCAR3細(xì)胞、MDA-MB-435 S細(xì)胞

NCI-H295R Cells;背景說明:腎上腺皮質(zhì)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:OCI-LY-8細(xì)胞、MIA-PaCa-2細(xì)胞、NCI-H1954細(xì)胞

SKNMC Cells;背景說明:這株細(xì)胞與HTB-11都是神經(jīng)源的。1971年9月分離得到SK-N-MC后,發(fā)現(xiàn)它有中性多巴胺-β-羥化酶活性,也有細(xì)胞內(nèi)兒茶胺,用甲醛可以誘導(dǎo)出熒光。;傳代方法:1:6-1:12傳代,每周2-3次換液。;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:KU812-F細(xì)胞、BC-028細(xì)胞、CAL 39細(xì)胞

SV-HUC-1 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:Neuro 2a細(xì)胞、NCI-UMC-11細(xì)胞、NCI-SNU-475細(xì)胞

SV-HUC-1 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:Neuro 2a細(xì)胞、NCI-UMC-11細(xì)胞、NCI-SNU-475細(xì)胞

H69/P 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次;生長特性:懸浮生長,聚團(tuán);形態(tài)特性:聚團(tuán)懸浮;相關(guān)產(chǎn)品有:Mo 59J細(xì)胞、SNU-1040細(xì)胞、HFT-8810細(xì)胞

Hs-940 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,2-3天換液1次。;生長特性:貼壁生長;形態(tài)特性:成纖維細(xì)胞;相關(guān)產(chǎn)品有:UCLA RO-81-A-1細(xì)胞、SK-Hep1細(xì)胞、751-NA-15細(xì)胞

PC10 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:MIMVEC細(xì)胞、BNCL2細(xì)胞、NCI-H2106細(xì)胞

2B4 Cells;背景說明:前列腺癌;骨轉(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:MOPC細(xì)胞、PK 15細(xì)胞、KY180細(xì)胞

SVGp12 Cells;背景說明:星形膠質(zhì)細(xì)胞;SV40轉(zhuǎn)化;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:H-2066細(xì)胞、SW-1573細(xì)胞、TE354T細(xì)胞

SUP-M2 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:SW1271細(xì)胞、D283MED細(xì)胞、Baby Hamster Kidney-21細(xì)胞

NCIH441 Cells;背景說明:NCI-H441建系于1982年(A.F.Gazdar,etal.)。該細(xì)胞分離自一名肺腺癌患者的心包液。該細(xì)胞能在半固體瓊脂糖中形成克隆,并能表達(dá)肺泡表面活性蛋白A。該細(xì)胞在有血清培養(yǎng)基中倍增時(shí)間為58小時(shí),在無血清培養(yǎng)基中倍增時(shí)間為99-138小時(shí)。;傳代方法:1:3傳代,2-3天傳一代;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:ASH-3細(xì)胞、HA細(xì)胞、A-204細(xì)胞

MonoMac1 Cells;背景說明:急性單核細(xì)胞白血病;男性;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:HSC-3細(xì)胞、95C細(xì)胞、C38細(xì)胞

Statens Seruminstitut Rabbit Cornea Cells;背景說明:角膜;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:SUDHL4細(xì)胞、HT細(xì)胞、HCEC-B4G12細(xì)胞

Silvanus Cells(提供STR鑒定圖譜)

ES-2 Cells;背景說明:ES-2細(xì)胞系源于一位47歲黑人女性的臨床卵巢透明細(xì)胞癌手術(shù)標(biāo)本。該細(xì)胞對(duì)中低劑量的阿霉素,順鉑,雙乙基亞硝脲,表鬼臼毒素吡喃葡糖苷等化療藥物有一定耐藥性。該細(xì)胞少量表達(dá)糖蛋白P。;傳代方法:1:3傳代,2-3天傳一次;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:OCI/AML-2細(xì)胞、GMK,BSC-1細(xì)胞、TOV-112細(xì)胞

Transformed Human Liver Epithelial-3 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:NRCC細(xì)胞、TE-1細(xì)胞、S.B.細(xì)胞

SCLC-21H Cells;背景說明: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。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SPCA-1細(xì)胞、NCIH2107細(xì)胞、231-luc細(xì)胞

H-1436 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:隨細(xì)胞的密度而增加;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:PNT1/A細(xì)胞、SUM-52-PE細(xì)胞、Hca-F細(xì)胞

TPC1 Cells;背景說明: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。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:TE-4細(xì)胞、Mono Mac 1細(xì)胞、U-373MG細(xì)胞

NEC8 Cells;背景說明:睪丸胚胎性癌;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:EB3 [Human Burkitt lymphoma]細(xì)胞、Rca-B細(xì)胞、KYSE410細(xì)胞

BALL1 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:懸浮生長;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:Wien 133細(xì)胞、HEH2細(xì)胞、UCLA-SO-M21細(xì)胞

NBL_S 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:KCL22細(xì)胞、HEK.EBNA細(xì)胞、Ocular Choroidal Melanoma-1細(xì)胞

HFL 1 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:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:MIA Paca2細(xì)胞、Panc 04.03細(xì)胞、HCC-1937細(xì)胞

HCC-2108 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:Human Embryonic Skin細(xì)胞、P3.653細(xì)胞、OCLY8細(xì)胞

P3-X63Ag8 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:HCC 2185細(xì)胞、B16/F0細(xì)胞、NUGC4細(xì)胞

MBVP Cells;背景說明:腦血管;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:COLO-16細(xì)胞、EOMA細(xì)胞、BMU-S1細(xì)胞

ACCM Cells;背景說明:涎腺腺樣囊性癌;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:QBI-HEK 293A細(xì)胞、ARH 77細(xì)胞、KG1A細(xì)胞

LS 1034 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3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:IAR 20細(xì)胞、HBE細(xì)胞、211H細(xì)胞

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

BayGenomics ES cell line CSI538 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RST648 Cells(提供STR鑒定圖譜)

C5-1X Cells(提供STR鑒定圖譜)

LL/2-mNIS-Neo/eGFP-Puro Cells(提供STR鑒定圖譜)

R/3.2-L Cells(提供STR鑒定圖譜)

RL34-HII 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.

Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.

Sci. Data 1:140035-140035(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=26586397; DOI=10.1007/s13277-015-4405-z

Zhang J., Wang D.-M., Hu N., Wang Q., Yu S., Wang J.

The construction and proliferative effects of a lentiviral vector capable of stably overexpressing SPINK1 gene in human pancreatic cancer AsPC-1 cell line.

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.

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=27910856; DOI=10.1038/cgt.2016.71; PMCID=PMC5159445

Mezencev R., Matyunina L.V., Wagner G.T., McDonald J.F.

Acquired resistance of pancreatic cancer cells to cisplatin is multifactorial with cell context-dependent involvement of resistance genes.

Cancer Gene Ther. 23:446-453(2016)


PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076

Li J., Zhao W., Akbani R., Liu W.-B., Ju Z.-L., Ling S.-Y., Vellano C.P., Roebuck P., Yu Q.-H., Eterovic A.K., Byers L.A., Davies M.A., Deng W.-L., Gopal Y.N.V., Chen G., von Euw E.M., Slamon D.J., Conklin D., Heymach J.V., Gazdar A.F., Minna J.D., Myers J.N., Lu Y.-L., Mills G.B., Liang H.

Characterization of human cancer cell lines by reverse-phase protein arrays.

Cancer Cell 31:225-239(2017)


PubMed=29444439; DOI=10.1016/j.celrep.2018.01.051; PMCID=PMC6343826

Yuan T.L., Amzallag A., Bagni R., Yi M., Afghani S., Burgan W., Fer N., Strathern L.A., Powell K., Smith B., Waters A.M., Drubin D.A., Thomson T., Liao R., Greninger P., Stein G.T., Murchie E., Cortez E., Egan R.K., Procter L., Bess M., Cheng K.T., Lee C.-S., Lee L.C., Fellmann C., Stephens R., Luo J., Lowe S.W., Benes C.H., McCormick F.

Differential effector engagement by oncogenic KRAS.

Cell Rep. 22:1889-1902(2018)


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)


PubMed=30971826; DOI=10.1038/s41586-019-1103-9

Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.

Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.

Nature 568:511-516(2019)


PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103

Ghandi M., Huang F.W., Jane-Valbuena J., Kryukov G.V., Lo C.C., McDonald E.R. 3rd, Barretina J.G., Gelfand E.T., Bielski C.M., Li H.-X., Hu K., Andreev-Drakhlin A.Y., Kim J., Hess J.M., Haas B.J., Aguet F., Weir B.A., Rothberg M.V., Paolella B.R., Lawrence M.S., Akbani R., Lu Y.-L., Tiv H.L., Gokhale P.C., de Weck A., Mansour A.A., Oh C., Shih J., Hadi K., Rosen Y., Bistline J., Venkatesan K., Reddy A., Sonkin D., Liu M., Lehar J., Korn J.M., Porter D.A., Jones M.D., Golji J., Caponigro G., Taylor J.E., Dunning C.M., Creech A.L., Warren A.C., McFarland J.M., Zamanighomi M., Kauffmann A., Stransky N., Imielinski M., Maruvka Y.E., Cherniack A.D., Tsherniak A., Vazquez F., Jaffe J.D., Lane A.A., Weinstock D.M., Johannessen C.M., Morrissey M.P., Stegmeier F., Schlegel R., Hahn W.C., Getz G., Mills G.B., Boehm J.S., Golub T.R., Garraway L.A., Sellers W.R.

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Nature 569:503-508(2019)"


關(guān)鍵字: AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中;傳代細(xì)胞;復(fù)蘇細(xì)胞;實(shí)驗(yàn)細(xì)胞;科研細(xì)胞;

公司簡介

上海冠導(dǎo)生物工程有限公司,先后從ATCC、DSMZ、ECACC、RIKEN、PromoCell、ScienCell、JCRB等國內(nèi)外細(xì)胞庫引進(jìn)細(xì)胞2000余株。以此為契機(jī),公司組建了冠導(dǎo)細(xì)胞庫,我司細(xì)胞均由資深細(xì)胞培養(yǎng)工程師進(jìn)行培養(yǎng)。我司可以提供的細(xì)胞有:①細(xì)胞系②原代細(xì)胞③穩(wěn)轉(zhuǎn)株④耐藥株⑤標(biāo)記細(xì)胞⑥細(xì)胞配套試劑等。
成立日期 2015-11-05 (10年) 注冊(cè)資本 100萬(元)
員工人數(shù) 50-100人 年?duì)I業(yè)額 ¥ 1000萬-5000萬
主營行業(yè) 細(xì)胞培養(yǎng),微生物學(xué),細(xì)胞生物學(xué) 經(jīng)營模式 工廠,試劑,定制,服務(wù)
  • 上海冠導(dǎo)生物工程有限公司
VIP 4年
  • 公司成立:10年
  • 注冊(cè)資本:100萬(元)
  • 企業(yè)類型:有限責(zé)任公司(自然人投資或控股)
  • 主營產(chǎn)品:①細(xì)胞系②原代細(xì)胞③穩(wěn)轉(zhuǎn)株④耐藥株⑤標(biāo)記細(xì)胞⑥細(xì)胞配套試劑等。
  • 公司地址:手機(jī)號(hào)/微信號(hào):18818239863 【QQ號(hào):3171921642】上海市張江高科技園區(qū)
詢盤

AsPC-1人轉(zhuǎn)移胰腺腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書相關(guān)廠家報(bào)價(jià)

更多
產(chǎn)品名稱 價(jià)格   公司名稱 報(bào)價(jià)日期
¥1680
VIP2年
廣州弗爾博生物科技有限公司
2025-02-24
¥1800
VIP4年
上海雅吉生物科技有限公司
2025-02-24
¥1500
VIP1年
上海晶風(fēng)生物科技有限公司
2025-02-24
詢價(jià)
VIP1年
上海賓穗生物科技有限公司
2025-02-24
¥1428
VIP5年
上海賓穗生物科技有限公司
2025-02-23
詢價(jià)
VIP6年
上海弘順生物科技有限公司
2025-02-23
¥1200
VIP3年
上海滬震實(shí)業(yè)有限公司
2025-02-21
詢價(jià)
深圳市豪地華拓生物科技有限公司
2025-02-18
¥10000
VIP3年
吉奧藍(lán)圖(廣東)生命科學(xué)技術(shù)中心
2025-01-21
詢價(jià)
武漢益普生物科技有限公司
2022-02-22
內(nèi)容聲明:
以上所展示的信息由商家自行提供,內(nèi)容的真實(shí)性、準(zhǔn)確性和合法性由發(fā)布商家負(fù)責(zé)。 商家發(fā)布價(jià)格指該商品的參考價(jià)格,并非原價(jià),該價(jià)格可能隨著市場(chǎng)變化,或是由于您購買數(shù)量不同或所選規(guī)格不同而發(fā)生變化。最終成交價(jià)格,請(qǐng)咨詢商家,以實(shí)際成交價(jià)格為準(zhǔn)。請(qǐng)意識(shí)到互聯(lián)網(wǎng)交易中的風(fēng)險(xiǎn)是客觀存在的