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[供應(yīng)]HTB-120 NCI-H128 人肺小細(xì)胞肺癌細(xì)胞

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更新時間:2025-02-08 21:00:08

有效期:2025年2月8日 -- 2025年8月8日

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簡單介紹 HTB-120 NCI-H128 人肺小細(xì)胞肺癌細(xì)胞,ATCC 細(xì)胞|細(xì)胞系|細(xì)胞株|腫瘤細(xì)胞|細(xì)胞;細(xì)胞庫管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)和*培養(yǎng)條件!

HTB-120 NCI-H128 人肺小細(xì)胞肺癌細(xì)胞

 

 

ATCC® Number: HTB-120™Price:$429.00
Designations:NCI-H128 [H128]
Depositors:AF Gazdar
Biosafety Level:1
Shipped:frozen
Medium & Serum:See Propagation
Growth Properties:floating aggregates
Organism:Homo sapiens
Morphology:floating aggregates         HTB-120 NCI-H128 人肺小細(xì)胞肺癌細(xì)胞
 
Source:Organ: lung
Disease: carcinoma; small cell lung cancer
Derived from metastatic site: pleural effusion
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. Please click here for information regarding the specific requirements for shipment to your location.
 
Tumorigenic:Yes
DNA Profile (STR):Amelogenin: X
CSF1PO: 10
D13S317: 12
D16S539: 13
D5S818: 9
D7S820: 8,10
THO1: 6,9
TPOX: 8
vWA: 17        HTB-120 NCI-H128 人肺小細(xì)胞肺癌細(xì)胞
Cytogenetic Analysis:There are 2 distinct aneuploid peaks, both have characteristic 3p deletion.
Isoenzymes:AK-1, 1
ES-D, 1
G6PD, A
GLO-I, 1-2
Me-2, 1
PGM1, 1
PGM3, 1
Age:60 years
Gender:male
Ethnicity:Black
Comments:This cell line is aneuploid.
Will form colonies in soft agar.
It retains small cell carcinoma morphology and ultrastructure as well as APUD cell characteristics.
NCI-H128 cells do well on a rotary shaker flask at 70 to 80 rpm at 37C.
It is normal for cultures of this line to have fairly large amounts of cell debris.
Propagation: ATCC complete growth medium: RPMI 1640 medium, 80%; fetal bovine serum, 20% - OR - Iscove's modified Dulbecco's medium, 80%; fetal bovine serum, 20%
Subculturing:Subc*tion Ratio: A subc*tion ratio of 1:2 to 1:4 is recommended
Medium Renewal: Twice per week
Allow cell aggregates to settle to the bottom of the flask, discard the supernatant medium, disperse the cells with gentle pipetting and dispense into new flasks. Subculture every 6 to 8 days.
Preservation:Culture medium, 90%; DMSO, 10%
Related Products:normal (or near-normal) cell line established from the same patient:ATCC CRL-5947
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
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
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
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         

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