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              人小細胞肺癌細胞;NCI-H69細胞

              • 產(chǎn)品型號:
              • 產(chǎn)品時間:2025-08-02
              • 簡要描述:上?;鄯f生物專業(yè)供應人小細胞肺癌細胞;NCI-H69細胞, 慧穎生物擁有完善的細胞庫和管理體系,細胞技術20%為博士學歷、40%為碩士學歷,自公司成立以來,慧穎細胞庫攜手合作單位,以每月平均近100株的量向高校、醫(yī)院、研究所等提供優(yōu)質細胞株細胞系。
              • 產(chǎn)品簡介

              人小細胞肺癌細胞;NCI-H69細胞

              數(shù)量:大量
              生長狀態(tài):懸浮生長,多細胞聚集
              細胞形態(tài):其他
              年限:55 years adult
              ATCC Number:HTB-119™
              相關疾病:小細胞肺癌
              是否是腫瘤細胞:1
              物種來源:
              運輸方式:凍存運輸
              器官來源:
              規(guī)格:0.1ml

              收到人小細胞肺癌細胞;NCI-H69細胞后的處理:

              1)收到細胞后,首先觀察瓶身是否完好(注意有無縫隙,裂痕)。

              2)顯微鏡下觀察細胞的生長狀況,有無細胞漂浮。

              3)用新潔爾滅消毒瓶口及瓶身。

              4)打開瓶口,再次用新潔爾滅消毒瓶口(可能會有液體溢出,注意不要碰到液體),酒精燈烤瓶口消毒。

              5)將培養(yǎng)液轉移至50ml離心管或廣口瓶中(若細胞漂浮嚴重,離心培養(yǎng)基,1000g*5分鐘,將離心后的培養(yǎng)基轉移至另一個大離心管中,留一點吹打細胞沉淀成懸液,回收細胞至原培養(yǎng)瓶),若漂浮不嚴重,亦離心一下。

              6)在原培養(yǎng)瓶中留一部分原裝培養(yǎng)液,再補加自己新配的培養(yǎng)基至適當容積,例如4ml,讓細胞適應一下環(huán)境。  當細胞長到70-80%,凍存大部分,小部分傳代。

              上?;鄯f生物專業(yè)供應 訂購:/!

              英文介紹:

              Source:

              Organ: lung 
              Disease: carcinoma; small cell lung cancer

               

              Permits/Forms:

              In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimay responsible for obtaining the permits. Pleaseclick here for information regarding the specific requirements for shipment to your location.

                  

              Receptors:

              insulin-like growth factor II (IGF II)

                

              Tumorigenic:

              Yes

                

              Oncogene:

              myc +; myb +; fes +; fms +; raf +; ras +

                

              DNA Profile (STR):

              CSF1PO: 10, 12 
              D13S317: 12 
              D16S539: 11 
              D5S818: 11, 13 
              D7S820: 9 
              THO1: 8, 9 
              TPOX: 10 
              vWA: 16, 17 
              Amelogenin: XY

                

              Cytogenetic Analysis:

              modal number = 76 to 78; range = 40 to 87
              This is an aneuploid human male cell line. Monosomy of many of the normal chromosomes is noted as well as bisomy in this subtetraploid cell line; however, translocations and deletions involving many of the missing chromosomes are noted, and these chromosomal rearrangements appear to be stable and generally paired. Twelve marker chromosomes were identified including: der(16)t(1;16)(q21;q23), der(22)t(4;22)(q12;q13), der(12)t(11;12)(q23;p12), del(17)(p11), der(19)t(5;19)(?q21;q13) and others.

                

              Isoenzymes:

              AK-1, 1 
              ES-D, 2 
              G6PD, B 
              GLO-I, 1-2 
              Me-2, 1 
              PGM1, 2 
              PGM3, 1

                

              Age:

              55 years adult

                

              Gender:

              male

                

              Ethnicity:

              Caucasian

                

              Comments:

              This cell line is aneuploid, will form colonies in soft agar and retains small cell carcinoma morphology and ultrastructure as well as APUD cell characteristics. 
              The cells grow in aggregates, thus cell counts are not accurate. 
              The cells stain positively for cytokeratins. 
              The line can be adapted to grow in shaker flask or spinner flask systems. 
              The N-myc gene is amplified, and there is expression of the mRNA and protein. 
              C-myc mRNA, but not protein, is expressed at a low level. 
              There is expression of c-myb, v-fes, v-fms, c-raf 1, Ha-ras, Ki-ras and N-ras mRNA.

                

              Propagation:

              ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
              Temperature: 37.0°C

                

              Subculturing:

              Protocol: Attached cells can be detached by shaking flask Allow aggregates to settle to the bottom of the flask, remove and discard the supernatant medium. Add fresh medium, disperse cells by gentle pipetting and dispense into new flasks. Do not break down aggregates. Subculture every 6 to 8 days. 
              Subc*tion Ratio: A subc*tion ratio of 1:2 to 1:4 is recommended 
              Medium Renewal: 2 times weekly

                

              Preservation:

              Freeze medium: Complete growth medium, 95%; DMSO, 5% 
              Storage temperature: liquid nitrogen vapor temperature

                

              Related Products:

              Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC30-2001
              recommended serum:ATCC 30-2020
              derivative:ATCC CRL-11351
              purified DNA:ATCC HTB-119D

                

              References:

              1805: Little CD, et al. Amplification and expression of the c-myc oncogene in human lung cancer cell lines. Nature 306: 194-196, 1983. PubMed: 6646201
              22250: Bepler G, et al. Expression of p64c-myc and neuroendocrine properties define three subclasses of small cell lung cancer. Oncogene 4: 45-50, 1989. PubMed: 2536917
              22446: Schardt C, et al. Characterization of insulin-like growth factor II receptors in human small cell lung cancer cell lines. Exp. Cell Res. 204: 22-29, 1993. PubMed: 8380141
              22465: Broers JL, et al. Spontaneous changes in intermediate filament protein expression patterns in lung cancer cell lines. J. Cell Sci. 91: 91-108, 1988. PubMed: 2473086
              22869: Rygaard K, et al. Expression of myc family oncoproteins in small-cell lung-cancer cell lines and xenografts. Int. J. Cancer 54: 144-152, 1993. PubMed: 8386707
              23036: Gazdar AF, et al. Establishment of continuous, clonable cultures of small-cell carcinoma of lung which have amine precursor uptake and decarboxylation cell properties. Cancer Res. 40: 3502-3507, 1980. PubMed:6108156
              23037: . . Cancer Res. 40: 4556-4563, 1980.
              23056: Carney DN, et al. Establishment and identification of small cell lung cancer cell lines having classic and variant features. Cancer Res. 45: 2913-2923, 1985. PubMed: 2985257
              23057: Gazdar AF, et al. Characterization of variant subclasses of cell lines derived from small cell lung cancer having distinctive biochemical, morphological, and growth properties. Cancer Res. 45: 2924-2930, 1985. PubMed: 2985258
              23065: Kiefer PE, et al. Amplification and expression of protooncogenes in human small cell lung cancer cell lines. Cancer Res. 47: 6236-6242, 1987. PubMed: 2824028
              23080: Hensel CH, et al. Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer. Cancer Res. 50: 3067-3072, 1990. PubMed: 2159370
              24389: . . Lung Cancer 4: 155-161, 1988.
              32276: Cairns P, et al. Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions. Cancer Res. 57: 5356-5359, 1997. PubMed: 9393760
              32488: Geiger T, et al. Antitumor activity of a PKC-alpha antisense oligonucleotide in combination with standard chemotherapeutic agents against various human tumors transplanted into nude mice. Anticancer Drug Des. 13: 35-45, 1998. PubMed: 9474241

               

               

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