131-94H4細胞 
	
		器官來源:	脾
	
	
		細胞形態:	**樣
	
	
		**類型:	IgG1 kappa
	
	
		生長狀態:	懸浮生長
	
	
		運輸方式:	凍存運輸
	
	
		年限:	*****
	
	
		數量:	大量
	
	
		是否是腫瘤細胞:	0
	
	
		物種來源:	小鼠
	
	
		品系:	129GIX+
	
	
		131-94H4細胞ATCC Number:	CRL-2739?
	
	
		Designations:	131-94H4
	
	
		Depositors:	 National Cancer Institute
	
	
		Isotype:	IgG1 kappa
	
	
		Biosafety Level:	1
	
	
		Shipped:	frozen
	
	
		Medium & Serum:	See Propagation
	
	
		Growth Properties:	suspension
	
	
		Organism:	Mus musculus (B cell); Mus musculus (myeloma) deposited as mouse (B cell); mouse (myeloma)
	
	
		Morphology:	lymphoblast
	
	
		
	
	
		Source:	Strain: 129GIX+
	
	
		Organ: spleen
	
	
		Cell Type: hybridoma: 131-94H4細胞B lymphocyte;
	
	
		Cellular Products:	immunoglobulin; monoclonal antibody; against a synthetic v-myb oncogene peptide
	
	
		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.
	
	
		Age:	*****
	
	
		Gender:	female
	
	
		Comments:	Animals were immunized with a synthetic polypeptide with the sequence RRKVEQEGYPQESSKAG(C) corresponding to peptides 119 to 135 of the MYB oncogene formerly v-myb (residues 2 to 18). Spleen cells were fused with Sp2/0 myeloma cells. Using immunoblot techniques, the antibody recognizes a 25 kd protein in BM2 cells and a protein of approximately 100 kd in Molt 4 cells. Protein is also detected in selected embryo tissues.The IgG1 and IgG2b reactivities of the antibody with the v-myb peptide (119 to 135) were confirmed by ELISA. IgG1 was strongly positive while IgG2b was only slightly reactive.
	
	
		Propagation: 131-94H4細胞ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. 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: Cultures can be maintained by the addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension at 1 to 2 X 10(5) viable cells/ml.
	
	
		Interval: Maintain cell density between 1 X 10(5) and 1 X 10(6) viable cells/ml.
	
	
		Medium Renewal: Add fresh medium every 2 to 3 days (depending on cell density)
	
	
		Preservation:	Freeze medium:131-94H4細胞 Complete growth medium supplemented with 5% (v/v) DMSO
	
	
		Storage temperature: liquid nitrogen vapor phase