A-498細胞 
	
		器官來源:	腎臟
	
	
		細胞形態:	上皮樣
	
	
		生長狀態:	貼壁生長
	
	
		數量:	大量
	
	
		運輸方式:	凍存運輸
	
	
		年限:	52 years
	
	
		ATCC Number:	HTB-44?
	
	
		相關**:	腫瘤
	
	
		是否是腫瘤細胞:	1
	
	
		物種來源:	人
	
	
		A-498細胞Designations:	A-498
	
	
		Depositors:	 W Nelson-Rees
	
	
		Biosafety Level:	1
	
	
		Shipped:	frozen
	
	
		Medium & Serum:	See Propagation
	
	
		Growth Properties:	adherent
	
	
		Organism:	Homo sapiens
	
	
		Morphology:	epithelial
	
	
		
	
	
		Source:	Organ: kidney
	
	
		Disease: carcinoma
	
	
		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: 11,12
	
	
		A-498細胞D13S317: 12
	
	
		D16S539: 12
	
	
		D5S818: 11,13
	
	
		D7S820: 10,11
	
	
		THO1: 6,9.3
	
	
		TPOX: 8,11
	
	
		vWA: 18
	
	
		Isoenzymes:	AK-1, 1
	
	
		ES-D, 2
	
	
		G6PD, B
	
	
		GLO-I, 2
	
	
		Me-2, 1
	
	
		PGM1, 1-2
	
	
		PGM3, 1
	
	
		Age:	52 years
	
	
		Gender:	female
	
	
		Comments:	S. Aaronson isolated this line using techniques as described for ATCC HTB-41.
	
	
		Propagation: A-498細胞ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
	
	
		Atmosphere: air, 95%; carbon dioxide (CO2), 5%
	
	
		Temperature: 37.0°C
	
	
		Subculturing:	Protocol:
	
	
		Remove and discard culture medium.
	
	
		Briefly rinse the cell layer with 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
	
	
		Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
	
	
		Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37C to facilitate dispersal.
	
	
		Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
	
	
		Add appropriate aliquots of the cell suspension to new culture vessels.
	
	
		Incubate cultures at 37C.
	
	
		
	
	
		Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:8 is recommended
	
	
		Medium Renewal: Twice per week
	
	
		Preservation: A-498細胞Freeze medium: culture medium, 95%; DMSO, 5%
	
	
		Storage temperature: liquid nitrogen vapor phase
	
	
		Related Products:	Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2003
	
	
		recommended serum:ATCC 30-2020
	
	
		0.25% (w/v) Trypsin - 0.53 mM EDTA in Hank' BSS (w/o Ca++, Mg++):ATCC 30-2101
	
	
		Cell culture tested DMSO:ATCC 4-X
	
	
		References:	22536: Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871
	
	
		22539: Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080
	
	
		23093: Faust JB, Meeker TC. Amplification and expression of the bcl-1 gene in human solid tumor cell lines. Cancer Res. 52: 2460-2463, 1992. PubMed: 1568216
	
	
		23218: Giard DJ, et al. In vitro cultivation of human tumors: establishment of cell lines derived from a series of solid tumors. J. Natl. Cancer Inst. 51: 1417-1423, 1973. PubMed: 4357758
	
	
		24381: Fogh J. Cultivation, characterization, and identification of human tumor cells with emphasis on kidney, testis, and bladder tumors. Natl. Cancer Inst. Monogr. 49: 5-9, 1978. PubMed: 571047