"NALM-6人B淋巴白血病細(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:懸浮生長(zhǎng)
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(yíng)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(lái)幫助它們的存活增殖,如果營(yíng)養(yǎng)物質(zhì)缺乏,細(xì)胞就會(huì)不生長(zhǎng)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(lái),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(lèi)、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(yíng)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(wú)菌的環(huán)境,一個(gè)小小的偏差,細(xì)胞就會(huì)死亡。
換液周期:每周2-3次
CCD 841 CoN Cells;背景說(shuō)明:結(jié)腸上皮細(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(shū);相關(guān)產(chǎn)品有:SUD4細(xì)胞、DF-1細(xì)胞、GM05887A細(xì)胞
RAMOS2G64C10 Cells;背景說(shuō)明:詳見(jiàn)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(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:McCoy細(xì)胞、MADB106細(xì)胞、U-87MG細(xì)胞
SNU16 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:3-4天換液1次。;生長(zhǎng)特性:懸浮聚集;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:CAL39細(xì)胞、FL 62891細(xì)胞、RIN14B細(xì)胞
NALM-6人B淋巴白血病細(xì)胞代次低|培養(yǎng)基|送STR圖譜
背景信息:急性B淋巴細(xì)胞白血??;男性
┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線(xiàn):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;
ATCC細(xì)胞庫(kù)(American Type Culture Colection),該中心一直致力于細(xì)胞分類(lèi)、鑒定和保藏工作。ATCC是全球最大的生物資源保藏中心,ATCC通過(guò)行業(yè)標(biāo)準(zhǔn)產(chǎn)品、服務(wù)和創(chuàng)新解決方案支持全球?qū)W術(shù)、政府、生物技術(shù)、制藥、食品、農(nóng)業(yè)和工業(yè)領(lǐng)域的科學(xué)進(jìn)步。ATCC提供的服務(wù)和定制解決方案包括細(xì)胞和微生物培養(yǎng)、鑒定、生物衍生物的開(kāi)發(fā)和生產(chǎn)、性能測(cè)試和生物資源保藏服務(wù)。美國(guó)國(guó)家標(biāo)準(zhǔn)協(xié)會(huì)(ANSI)認(rèn)可了ATCC標(biāo)準(zhǔn)開(kāi)發(fā)組織,并制定了標(biāo)準(zhǔn)協(xié)議,以確保生物材料的可靠性和可重復(fù)性。ATCC的使命是為了獲取、鑒定、保存、開(kāi)發(fā)、標(biāo)準(zhǔn)化和分發(fā)生物資源和生物信息,以提高和應(yīng)用生物科學(xué)知識(shí)。
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)
NALM-6人B淋巴白血病細(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
OLN-93 Cells;背景說(shuō)明:膠質(zhì)細(xì)胞;自發(fā)永生;Wistar;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(shū);相關(guān)產(chǎn)品有:SRA 01/04細(xì)胞、C3H/10T1/2細(xì)胞、NS1/1-Ag4.1細(xì)胞
Hs695 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,2-3天換液1次。;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:NB4細(xì)胞、C-33-A細(xì)胞、M109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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:L cells (TK-)細(xì)胞、TK 10細(xì)胞、MGc80-3細(xì)胞
CEM-C7 Cells;背景說(shuō)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(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:CAL120細(xì)胞、NOMO-1細(xì)胞、Farage OL細(xì)胞
┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線(xiàn):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:淋巴母細(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(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(kāi)。(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(zhuān)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(wú)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(zhǎng)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(wú)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(wú)勾。冷凍管要將蓋子蓋緊,并標(biāo)記HAO細(xì)胞名稱(chēng)和凍存日期,同時(shí)作HAO登記(日期、細(xì)胞種類(lèi)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(guò)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(zhǎng)期保存,但為妥善起見(jiàn),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(zhǎng)情況,然后再繼續(xù)凍存。
A431/P Cells;背景說(shuō)明:該細(xì)胞源自一位患有皮膚鱗狀細(xì)胞癌的85歲女性,是GiardDJ等人建立的一系列細(xì)胞株中的一株。該細(xì)胞在免疫抑制小鼠體內(nèi)可成瘤,在瓊脂上培養(yǎng)可形成克??;是一個(gè)超三倍體人細(xì)胞株。;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:NCIH2135細(xì)胞、MCF12F細(xì)胞、LMTK-細(xì)胞
H82sclc 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:懸浮生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:Y 1細(xì)胞、SCC-4細(xì)胞、Pro-5WgaRI3C細(xì)胞
CEM-C1 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(shū);相關(guān)產(chǎn)品有:Reuber H35細(xì)胞、AG06814-J細(xì)胞、Hs 729細(xì)胞
NCIH740 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:95C細(xì)胞、NCI-H3255細(xì)胞、CCC-HHM-2細(xì)胞
LSECs 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:NCI-H295細(xì)胞、QGY7701細(xì)胞、DHL10細(xì)胞
HPDLF Cells;背景說(shuō)明:牙周膜;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(shū);相關(guān)產(chǎn)品有:HCC2935細(xì)胞、MLO-Y4細(xì)胞、J774 A.1細(xì)胞
VMRCLCD 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:L-5178-Y-R細(xì)胞、PaTu-8988s細(xì)胞、Astrocyte type I clone細(xì)胞
HUSMC Cells;背景說(shuō)明:子宮;平滑肌細(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(shū);相關(guān)產(chǎn)品有:H-847細(xì)胞、Hep G2細(xì)胞、COLO 320F細(xì)胞
COLO.205 Cells;背景說(shuō)明:該細(xì)胞系是1957年由T.U.Sample等從患有結(jié)腸癌的70歲男性白人的腹水中分離的。該病人在取腹水樣品前已用5-尿嘧啶治療4~6周。角蛋白免疫過(guò)氧化物酶染色陽(yáng)性;產(chǎn)生CEA、IL10。;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:PC3細(xì)胞、RCM1細(xì)胞、NCI-1155細(xì)胞
NCI-H2023 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:每周換液2次;生長(zhǎng)特性:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:G-292細(xì)胞、Stanford University-Diffuse Histiocytic Lymphoma-5細(xì)胞、HOS (TE85)細(xì)胞
HEp-2 Cells;背景說(shuō)明:最初認(rèn)為這個(gè)細(xì)胞源自喉上皮癌,但隨后通過(guò)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(guò)氧化物酶染色陽(yáng)性。;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:Jurkat-E6細(xì)胞、HCC38細(xì)胞、beta TC6細(xì)胞
H508 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(shū);相關(guān)產(chǎn)品有:ADR-RES細(xì)胞、U 138 MG細(xì)胞、H-1819細(xì)胞
H1770 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:隨細(xì)胞的生長(zhǎng)而換液;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(shū);相關(guān)產(chǎn)品有:H-209細(xì)胞、HuH1細(xì)胞、Ku812細(xì)胞
T98-G Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:按1:3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(shū);相關(guān)產(chǎn)品有:H-28細(xì)胞、D341 Med細(xì)胞、OV1/P細(xì)胞
TOV-112 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,3-4天換液1次。;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:SW-626細(xì)胞、RWPE2細(xì)胞、RCSMC細(xì)胞
OKT 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:SNU-638細(xì)胞、ROS17/2.8細(xì)胞、SK-N-BE(2)-M17細(xì)胞
NG-108-15 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:TC-1 [Mouse lung]細(xì)胞、CL11細(xì)胞、BNL CL.2細(xì)胞
Abcam A-549 OAS3 KO Cells(提供STR鑒定圖譜)
AC1-1 Cells(提供STR鑒定圖譜)
BayGenomics ES cell line CSH053 Cells(提供STR鑒定圖譜)
BayGenomics ES cell line RRU422 Cells(提供STR鑒定圖譜)
BBdF-1 Cells(提供STR鑒定圖譜)
CHO-hGluN1-hGluN2D Cells(提供STR鑒定圖譜)
DA02529 Cells(提供STR鑒定圖譜)
DA05485 Cells(提供STR鑒定圖譜)
Genomeditech HCT116 H_CDH17 Cells(提供STR鑒定圖譜)
OCILY7 Cells;背景說(shuō)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(zhǎng)特性:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:SNU-520細(xì)胞、PT-67細(xì)胞、Hs839T細(xì)胞
NALM-6人B淋巴白血病細(xì)胞代次低|培養(yǎng)基|送STR圖譜
RAT2 Cells;背景說(shuō)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(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:Rat 2細(xì)胞、Walker256細(xì)胞、P31 FUJ細(xì)胞
LTEPa2 Cells;背景說(shuō)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(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:SNU-484細(xì)胞、PTK-1細(xì)胞、MADB106細(xì)胞
Tb 1 Lu Cells;背景說(shuō)明:肺;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(shū);相關(guān)產(chǎn)品有:MCF.10A細(xì)胞、BEL 7402細(xì)胞、NHRF細(xì)胞
COLO 206 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:H-1650細(xì)胞、MC-3T3-E1細(xì)胞、HEC-1-A細(xì)胞
GM02219D Cells;背景說(shuō)明:MOLT-4與MOLT-3來(lái)源于一名19歲的男性急性淋巴細(xì)胞性白血病的復(fù)發(fā)患者,該患者前期接受過(guò)多種藥物聯(lián)合化療。MOLT-4細(xì)胞系為T(mén)淋巴細(xì)胞起源,p53基因的第248位密碼子有一個(gè)G→A突變,不表達(dá)p53,不表達(dá)免疫球蛋白或EB病毒;可產(chǎn)生高水平的末端脫氧核糖轉(zhuǎn)移酶;表達(dá)CD1(49%),CD2(35%),CD3A(26%)B(33%)C(34%),CD4(55%),CD5(72%),CD6(22%),CD7(77%)。;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;圓形;相關(guān)產(chǎn)品有:RMa-bm細(xì)胞、WSU-DLCL2細(xì)胞、HFT8810細(xì)胞
1E9A4A4 Cells(提供STR鑒定圖譜)
MES-SA Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:6-1:8?jìng)鞔?;每周?3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:MCF-12A細(xì)胞、SUNE 1細(xì)胞、6-10B細(xì)胞
MonoMac6 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:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:DMS53細(xì)胞、SUM190細(xì)胞、NCI-H810細(xì)胞
BEND Cells;背景說(shuō)明:子宮內(nèi)膜;上皮細(xì)胞;雌性;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(shū);相關(guān)產(chǎn)品有:SJ-Rh 30細(xì)胞、HBMEC細(xì)胞、MOLP-2細(xì)胞
KM.12 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:HFLS細(xì)胞、GM02131細(xì)胞、SK HEP 01細(xì)胞
IHC-ST1 Cells;背景說(shuō)明:肝內(nèi)膽管癌;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(shū);相關(guān)產(chǎn)品有:Be-Wo細(xì)胞、H-3255細(xì)胞、HPC-Y5細(xì)胞
SKRC-42 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:H-1618細(xì)胞、Ra No. 1細(xì)胞、NK-92MI細(xì)胞
NCIH82 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:懸浮生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:HT55細(xì)胞、NTera 2細(xì)胞、Stanford University-Diffuse Histiocytic Lymphoma-1細(xì)胞
IM9 Cells;背景說(shuō)明:B淋巴細(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:懸浮;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:Chang Cells細(xì)胞、W256細(xì)胞、FTC133細(xì)胞
h-pES10 Cells(提供STR鑒定圖譜)
HAP1 PSMB8 (-) 3 Cells(提供STR鑒定圖譜)
SU-86-86 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(shū);相關(guān)產(chǎn)品有:HCA 7細(xì)胞、NCIH820細(xì)胞、OVCA8細(xì)胞
PLA802 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(shū);相關(guān)產(chǎn)品有:CaES-17細(xì)胞、HS-5細(xì)胞、CCD-19Lu細(xì)胞
C-33 A Cells;背景說(shuō)明:C-33A細(xì)胞株是N. Auersperg從宮頸癌切片中建立的一系列細(xì)胞株(參見(jiàn)ATCC CRL-1594和ATCC CRL-1595)中的一株。 細(xì)胞一開(kāi)始就表現(xiàn)出亞二倍體核型及上皮細(xì)胞形態(tài)。 連續(xù)傳代可以觀察到核型不穩(wěn)定。 存在成視網(wǎng)膜細(xì)胞瘤蛋白(pRB),但大小不正常。 P53表達(dá)上調(diào),且有一個(gè)273位密碼子的點(diǎn)突變導(dǎo)致Arg -> Cys的替換。 人乳頭瘤病毒DNA及RNA陰性。;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:ST2細(xì)胞、KRC-Y細(xì)胞、VP 229細(xì)胞
GLC82 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:NCTC 929細(xì)胞、Panc5.04細(xì)胞、TE-8細(xì)胞
TU 686 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(shū);相關(guān)產(chǎn)品有:NF639細(xì)胞、KOPN8細(xì)胞、N-Tera-2細(xì)胞
Immortalized Human Hepatocytes Cells;背景說(shuō)明:肝;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(shū);相關(guān)產(chǎn)品有:H-7721細(xì)胞、H-774細(xì)胞、CaES-17細(xì)胞
UACC 812 Cells;背景說(shuō)明:該細(xì)胞是由Liebovitz A等于1986年從一名43歲的白人女性乳腺導(dǎo)管癌患者的乳腺切除腫瘤組織中分離建立的;手術(shù)前該病人曾接受過(guò)廣泛的化療。該細(xì)胞HER-2/neu癌基因序列有15倍的擴(kuò)增;雌激素受體ER、孕激素受體PR和糖蛋白P陰性。;傳代方法:1:3傳代;5-7天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:RL-952細(xì)胞、VMM5細(xì)胞、Tu212細(xì)胞
H1869 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次。;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:PA12細(xì)胞、SW900細(xì)胞、H283細(xì)胞
Huh-7.5 Cells(提供STR鑒定圖譜)
L.P3 Q-2 Cells(提供STR鑒定圖譜)
MSHRIe002-A-SOX17 control 1 Cells(提供STR鑒定圖譜)
OH94 Cells(提供STR鑒定圖譜)
ROS-17 Cells(提供STR鑒定圖譜)
Ubigene A-549 PKN2 KO Cells(提供STR鑒定圖譜)
UTA.01006.WT Cells(提供STR鑒定圖譜)
HAP1 VIMP (-) 1 Cells(提供STR鑒定圖譜)
PA317 Cells;背景說(shuō)明:胚胎;成纖維細(xì)胞;NIH Swiss;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(shū);相關(guān)產(chǎn)品有:R 2 C細(xì)胞、Panc04.03細(xì)胞、H3396細(xì)胞
SNK6 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(shū);相關(guān)產(chǎn)品有:BJA-B1細(xì)胞、H69C細(xì)胞、CCC-HPF-1細(xì)胞
PL-45 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:KPNRTBM1細(xì)胞、SAOS 2細(xì)胞、DHL-4細(xì)胞
MC57G Cells;背景說(shuō)明:纖維肉瘤;C57BL/6J;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(shū);相關(guān)產(chǎn)品有:HTR8svn細(xì)胞、MIA Paca2細(xì)胞、HT144細(xì)胞
NCI-HUT-520 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:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:P3J HR-1細(xì)胞、RS(4;11)細(xì)胞、MF2059細(xì)胞
NCI-HUT-520 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:貼壁或懸浮,詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:P3J HR-1細(xì)胞、RS(4;11)細(xì)胞、MF2059細(xì)胞
CLONE M3 Cells;背景說(shuō)明:黑色素瘤;雄性;DBA;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(shū);相關(guān)產(chǎn)品有:P3-X63-Ag 8.653細(xì)胞、A3細(xì)胞、HPAF-II細(xì)胞
Blotchy fibroblast-11 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:Mevo細(xì)胞、OCI-AML-3細(xì)胞、UMC11細(xì)胞
HEK/293 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:VMM5A細(xì)胞、Human Corneal Epithelial cells-Transformed細(xì)胞、L-M[TK-]細(xì)胞
HuT-78 Cells;背景說(shuō)明:皮膚;T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(shū);相關(guān)產(chǎn)品有:LLC-PK1細(xì)胞、University of Arizona Cell Culture-812細(xì)胞、LS-513細(xì)胞
NCI-SNU-216 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(shū);相關(guān)產(chǎn)品有:KPL4細(xì)胞、ANA-1細(xì)胞、H4-II-EC3細(xì)胞
NCI-SNU-C2B 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:X63-Ag8細(xì)胞、SUM 52細(xì)胞、GL261細(xì)胞
S3 HeLa Cells;背景說(shuō)明:該細(xì)胞是1955年由PuckTT,MarcusPI和CieciuraSJ建系的,含HPV-18序列;角蛋白陽(yáng)性;可用于與染色體突變、細(xì)胞營(yíng)養(yǎng)、集落形成相關(guān)的哺乳動(dòng)物細(xì)胞的克隆分析。;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:MDA-MB 231細(xì)胞、MPVECs細(xì)胞、Melan-a細(xì)胞
C-Li-7 Cells;背景說(shuō)明:人肝癌細(xì)胞株。這株細(xì)胞從裸鼠體外移植瘤中建立。;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(shū);相關(guān)產(chǎn)品有:SW-780細(xì)胞、SJSA1細(xì)胞、KU 812F細(xì)胞
C4-2B Cells;背景說(shuō)明:前列腺癌;左鎖骨上淋巴結(jié)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:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:H-II-E-C3細(xì)胞、FRO81-2細(xì)胞、LCD細(xì)胞
SZ-NF6 Cells(提供STR鑒定圖譜)
AML193 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。3天內(nèi)可長(zhǎng)滿(mǎn)。;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:NCIH146細(xì)胞、MOLP2細(xì)胞、GM01232E細(xì)胞
H-250 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(shū);相關(guān)產(chǎn)品有:H520細(xì)胞、Functional Liver Cell-7細(xì)胞、OUMS-27細(xì)胞
SNU-C1 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:每3-5天換液。;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:NGP細(xì)胞、GLAG-66細(xì)胞、Ly7細(xì)胞
A875 Cells;背景說(shuō)明:NGF受體陽(yáng)性。;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:多角形;相關(guān)產(chǎn)品有:SNU182細(xì)胞、U2932細(xì)胞、H820細(xì)胞
BE(2)M-17 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(shū)部分;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:P3X63 AG8-653細(xì)胞、GM00637B細(xì)胞、50.B1細(xì)胞
BE(2)C Cells;背景說(shuō)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(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);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
NALM-6人B淋巴白血病細(xì)胞代次低|培養(yǎng)基|送STR圖譜
UMUC-14 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(shū);相關(guān)產(chǎn)品有:HCAEC細(xì)胞、NS-20Y細(xì)胞、CTLL2細(xì)胞
NRK clone 52E 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:PBL細(xì)胞、ARO81細(xì)胞、NIH:OVCAR-5細(xì)胞
SW-403 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:2—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:上皮細(xì)胞;相關(guān)產(chǎn)品有:TF-1a細(xì)胞、HSC5細(xì)胞、Lewis-Lung細(xì)胞
J-111 Cells;背景說(shuō)明:?jiǎn)魏思?xì)胞白血病;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(shū);相關(guān)產(chǎn)品有:Vero 76 clone E6細(xì)胞、Hs940.T細(xì)胞、HME1細(xì)胞
DSL6A/C1 Cells;背景說(shuō)明:胰腺癌;雄性;Lewis;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(shū);相關(guān)產(chǎn)品有:HSC-4細(xì)胞、293T/17細(xì)胞、OVCAR433細(xì)胞
MEL-526 Cells;背景說(shuō)明:黑色素瘤;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(shū);相關(guān)產(chǎn)品有:Tj-905細(xì)胞、D283-MED細(xì)胞、Panc 03.27細(xì)胞
P3JHR-1 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:每2-3天換液;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:L02細(xì)胞、HTh-74細(xì)胞、COLO320-DM細(xì)胞
Ca 9-22 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:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:SCH細(xì)胞、C4-2B細(xì)胞、Anip 973細(xì)胞
BayGenomics ES cell line RRR323 Cells(提供STR鑒定圖譜)
BayGenomics ES cell line YHD299 Cells(提供STR鑒定圖譜)
HTK Cells(提供STR鑒定圖譜)
PCRP-HOXB9-1E6 Cells(提供STR鑒定圖譜)
F2408-No.7 Cells(提供STR鑒定圖譜)
HPS3191 Cells(提供STR鑒定圖譜)
" "PubMed=2985879; DOI=10.1016/0145-2126(85)90084-0
Drexler H.G., Gaedicke G., Minowada J.
Isoenzyme studies in human leukemia-lymphoma cell lines -- 1 carboxylic esterase.
Leuk. Res. 9:209-229(1985)
PubMed=3159941; DOI=10.1016/0145-2126(85)90134-1
Drexler H.G., Gaedicke G., Minowada J.
Isoenzyme studies in human leukemia-lymphoma cell lines -- III Beta-hexosaminidase (E.C. 3.2.1.30).
Leuk. Res. 9:549-559(1985)
PubMed=3874327; DOI=10.1016/0145-2126(85)90133-x
Drexler H.G., Gaedicke G., Minowada J.
Isoenzyme studies in human leukemia-lymphoma cells lines -- II. Acid phosphatase.
Leuk. Res. 9:537-548(1985)
PubMed=2415623; DOI=10.4049/jimmunol.136.1.320
Goldmacher V.S., Lambert J.M., Young A.Y., Anderson J., Tinnel N.L., Kornacki M., Ritz J., Blattler W.A.
Expression of the common acute lymphoblastic leukemia antigen (CALLA) on the surface of individual cells of human lymphoblastoid lines.
J. Immunol. 136:320-325(1986)
PubMed=2939141; DOI=10.4049/jimmunol.136.11.4311
Pesando J.M., Graf L.
Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells.
J. Immunol. 136:4311-4318(1986)
PubMed=2783384
Luo Y., Hara H., Haruta Y., Seon B.K.
Establishment of ascitic tumor of human pre-B acute lymphoblastic leukemia in nonconditioned nude mice.
Cancer Res. 49:706-710(1989)
PubMed=2140233; DOI=10.1111/j.1440-1827.1990.tb01549.x
Nakano A., Harada T., Morikawa S., Kato Y.
Expression of leukocyte common antigen (CD45) on various human leukemia/lymphoma cell lines.
Acta Pathol. Jpn. 40:107-115(1990)
PubMed=8847894
Tani A., Tatsumi E., Nakamura F., Kumagai S., Kosaka Y., Sano K., Nakamura H., Amakawa R., Ohno H.
Sensitivity to dexamethasone and absence of bcl-2 protein in Burkitt's lymphoma cell line (Black93) derived from a patient with acute tumor lysis syndrome: comparative study with other BL and non-BL lines.
Leukemia 10:1592-1603(1996)
PubMed=9067587; DOI=10.1038/sj.leu.2400571
Uphoff C.C., MacLeod R.A.F., Denkmann S.A., Golub T.R., Borkhardt A., Janssen J.W.G., Drexler H.G.
Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines.
Leukemia 11:441-447(1997)
PubMed=9510473; DOI=10.1111/j.1349-7006.1998.tb00476.x; PMCID=PMC5921588
Hosoya N., Hangaishi A., Ogawa S., Miyagawa K., Mitani K., Yazaki Y., Hirai H.
Frameshift mutations of the hMSH6 gene in human leukemia cell lines.
Jpn. J. Cancer Res. 89:33-39(1998)
PubMed=9680106; DOI=10.1016/S0145-2126(98)00050-2
Matsuo Y., Drexler H.G.
Establishment and characterization of human B cell precursor-leukemia cell lines.
Leuk. Res. 22:567-579(1998)
PubMed=9738977; DOI=10.1111/j.1349-7006.1998.tb03275.x; PMCID=PMC5921886
Takizawa J., Suzuki R., Kuroda H., Utsunomiya A., Kagami Y., Joh T., Aizawa Y., Ueda R., Seto M.
Expression of the TCL1 gene at 14q32 in B-cell malignancies but not in adult T-cell leukemia.
Jpn. J. Cancer Res. 89:712-718(1998)
PubMed=10490826; DOI=10.1038/sj.onc.1202874
Fu X.-Y., McGrath S., Pasillas M., Nakazawa S., Kamps M.P.
EB-1, a tyrosine kinase signal transduction gene, is transcriptionally activated in the t(1;19) subset of pre-B ALL, which express oncoprotein E2a-Pbx1.
Oncogene 18:4920-4929(1999)
PubMed=10695022
Matsuo Y., Nishizaki C., Drexler H.G.
Efficient DNA fingerprinting method for the identification of cross-culture contamination of cell lines.
Hum. Cell 12:149-154(1999)
PubMed=10739008; DOI=10.1016/S0145-2126(99)00182-4
Inoue K., Kohno T., Takakura S., Hayashi Y., Mizoguchi H., Yokota J.
Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines.
Leuk. Res. 24:255-262(2000)
PubMed=11021758; DOI=10.1038/sj.leu.2401891
Majka M., Rozmyslowicz T., Honczarenko M.J., Ratajczak J., Wasik M.A., Gaulton G.N., Ratajczak M.Z.
Biological significance of the expression of HIV-related chemokine coreceptors (CCR5 and CXCR4) and their ligands by human hematopoietic cell lines.
Leukemia 14:1821-1832(2000)
DOI=10.1016/B978-0-12-221970-2.50457-5
Drexler H.G.
The leukemia-lymphoma cell line factsbook.
(In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001)
PubMed=11226526; DOI=10.1016/S0145-2126(00)00121-1
Inoue K., Kohno T., Takakura S., Hayashi Y., Mizoguchi H., Yokota J.
Corrigendum to: Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines Leukemia Research 24 (2000), 255-262.
Leuk. Res. 25:275-278(2001)
PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459
Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.
Short tandem repeat profiling provides an international reference standard for human cell lines.
Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)
PubMed=11986953; DOI=10.1038/sj.leu.2402485
O'Donnell P.H., Guo W.-X., Reynolds C.P., Maurer B.J.
N-(4-hydroxyphenyl)retinamide increases ceramide and is cytotoxic to acute lymphoblastic leukemia cell lines, but not to non-malignant lymphocytes.
Leukemia 16:902-910(2002)
PubMed=15843827; DOI=10.1038/sj.leu.2403749
Andersson A., Eden P., Lindgren D., Nilsson J., Lassen C., Heldrup J., Fontes M., Borg A., Mitelman F., Johansson B., Hoglund M., Fioretos T.
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations.
Leukemia 19:1042-1050(2005)
PubMed=16405397; DOI=10.1089/dna.2006.25.19
Adachi N., So S., Iiizumi S., Nomura Y., Murai K., Yamakawa C., Miyagawa K., Koyama H.
The human pre-B cell line Nalm-6 is highly proficient in gene targeting by homologous recombination.
DNA Cell Biol. 25:19-24(2006)
PubMed=16408098; DOI=10.1038/sj.leu.2404081
Quentmeier H., MacLeod R.A.F., Zaborski M., Drexler H.G.
JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.
Leukemia 20:471-476(2006)
PubMed=16969076; DOI=10.4161/cbt.5.8.3251; PMCID=PMC2714972
Edkins S., O'Meara S., Parker A., Stevens C., Reis M., Jones S., Greenman C.D., Davies H.R., Dalgliesh G.L., Forbes S., Hunter C., Smith R., Stephens P.J., Goldstraw P., Nicholson A., Chan T.-L., Velculescu V.E., Yuen S.T., Leung S.Y., Stratton M.R., Futreal P.A.
Recurrent KRAS codon 146 mutations in human colorectal cancer.
Cancer Biol. Ther. 5:928-932(2006)
PubMed=20103924
Adachi N., Nishijima H., Shibahara K.-i.
Gene targeting using the human Nalm-6 pre-B cell line.
Biosci. Trends 2:169-180(2008)
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=20575032; DOI=10.1002/ajh.21738; PMCID=PMC7159455
Inukai T., Zhang X.-R., Kameyama T., Suzuki Y., Yoshikawa K., Kuroda I., Nemoto A., Akahane K., Sato H., Goi K., Nakamoto K., Hamada J.-i., Tada M., Moriuchi T., Sugita K.
A specific linkage between the incidence of TP53 mutations and type of chromosomal translocations in B-precursor acute lymphoblastic leukemia cell lines.
Am. J. Hematol. 85:535-537(2010)
PubMed=20922763; DOI=10.1002/pbc.22801; PMCID=PMC3005554
Kang M.H., Smith M.A., Morton C.L., Keshelava N., Houghton P.J., Reynolds C.P.
National Cancer Institute pediatric preclinical testing program: model description for in vitro cytotoxicity testing.
Pediatr. Blood Cancer 56:239-249(2011)
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=23596518; DOI=10.1371/journal.pone.0061189; PMCID=PMC3626652
Suzuki T., Ukai A., Honma M., Adachi N., Nohmi T.
Restoration of mismatch repair functions in human cell line Nalm-6, which has high efficiency for gene targeting.
PLoS ONE 8:E61189-E61189(2013)
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=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=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=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=29786757; DOI=10.1007/s12185-018-2474-7
Tomoyasu C., Imamura T., Tomii T., Yano M., Asai D., Goto H., Shimada A., Sanada M., Iwamoto S., Takita J., Minegishi M., Inukai T., Sugita K., Hosoi H.
Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes.
Int. J. Hematol. 108:312-318(2018)
PubMed=30285677; DOI=10.1186/s12885-018-4840-5; PMCID=PMC6167786
Tan K.-T., Ding L.-W., Sun Q.-Y., Lao Z.-T., Chien W., Ren X., Xiao J.-F., Loh X.-Y., Xu L., Lill M., Mayakonda A., Lin D.-C., Yang H.H., Koeffler H.P.
Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines.
BMC Cancer 18:940.1-940.13(2018)
PubMed=30629668; DOI=10.1371/journal.pone.0210404; PMCID=PMC6328144
Uphoff C.C., Pommerenke C., Denkmann S.A., Drexler H.G.
Screening human cell lines for viral infections applying RNA-Seq data analysis.
PLoS ONE 14:E0210404-E0210404(2019)
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=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)
PubMed=31160637; DOI=10.1038/s41598-019-44491-x; PMCID=PMC6547646
Quentmeier H., Pommerenke C., Dirks W.G., Eberth S., Koeppel M., MacLeod R.A.F., Nagel S., Steube K.G., Uphoff C.C., Drexler H.G.
The LL-100 panel: 100 cell lines for blood cancer studies.
Sci. Rep. 9:8218-8218(2019)
PubMed=31243274; DOI=10.1038/s41467-019-10637-8; PMCID=PMC6594946
Tian L.-Q., Shao Y., Nance S., Dang J.-J., Xu B.-S., Ma X.-T., Li Y.-J., Ju B.-S., Dong L., Newman S., Zhou X., Schreiner P., Tseng E., Hon T., Ashby M., Li C.-L., Easton J., Gruber T.A., Zhang J.-H.
Long-read sequencing unveils IGH-DUX4 translocation into the silenced IGH allele in B-cell acute lymphoblastic leukemia.
Nat. Commun. 10:2789.1-2789.10(2019)
PubMed=31978347; DOI=10.1016/j.cell.2019.12.023; PMCID=PMC7339254
Nusinow D.P., Szpyt J., Ghandi M., Rose C.M., McDonald E.R. 3rd, Kalocsay M., Jane-Valbuena J., Gelfand E.T., Schweppe D.K., Jedrychowski M.P., Golji J., Porter D.A., Rejtar T., Wang Y.K., Kryukov G.V., Stegmeier F., Erickson B.K., Garraway L.A., Sellers W.R., Gygi S.P.
Quantitative proteomics of the Cancer Cell Line Encyclopedia.
Cell 180:387-402.e16(2020)
PubMed=34823530; DOI=10.1186/s12935-021-02335-7; PMCID=PMC8614043
Li Y.-Y., Zuo C., Gu L.
Characterization of a novel glucocorticoid-resistant human B-cell acute lymphoblastic leukemia cell line, with AMPK, mTOR and fatty acid synthesis pathway inhibition.
Cancer Cell Int. 21:623.1-623.14(2021)"
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