NCI-H128細胞 
	
		是否是腫瘤細胞:	1
	
	
		物種來源:	人
	
	
		年限:	60 years
	
	
		數量:	大量
	
	
		生長狀態:	漂浮生長
	
	
		細胞形態:	其他
	
	
		ATCC Number:	HTB-120?
	
	
		相關**:	小細胞肺癌
	
	
		器官來源:	肺
	
	
		運輸方式:	凍存運輸
	
	
		Designations:	NCI-H128 [H128]
	
	
		Depositors:	 AF Gazdar
	
	
		NCI-H128細胞Biosafety Level:	1
	
	
		Shipped:	frozen
	
	
		Medium & Serum:	See Propagation
	
	
		Growth Properties:	floating aggregates
	
	
		Organism:	Homo sapiens
	
	
		Morphology:	floating aggregates
	
	
		
	
	
		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 ultimately 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
	
	
		Cytogenetic Analysis: NCI-H128細胞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:	Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
	
	
		Medium Renewal: Twice per week
	
	
		NCI-H128細胞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. NCI-H128細胞Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions. Cancer Res. 57: 5356-5359, 1997. PubMed: 9393760