WERI-Rb-1細(xì)胞，人視網(wǎng)膜神經(jīng)膠質(zhì)瘤細(xì)胞

簡(jiǎn)要描述：WERI-Rb-1細(xì)胞，人視網(wǎng)膜神經(jīng)膠質(zhì)瘤細(xì)胞
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WERI-Rb-1細(xì)胞，人視網(wǎng)膜神經(jīng)膠質(zhì)瘤細(xì)胞

Designations:	WERI-Rb-1
Depositors:	TW Sery
Biosafety Level:	1
Shipped:	frozen
Medium & Serum:	See Propagation
Growth Properties:	susopension
Organism:	Hom sapiens
Morphology:	grape-like clusters of round cells
Source:	Organ: eye Tissue: retina Disease: retinoblastoma
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.
Isolation:	Isolation date: 1974
Applications:	transfection host
Tumorigenic:	Yes WERI-Rb-1細(xì)胞，人視網(wǎng)膜神經(jīng)膠質(zhì)瘤細(xì)胞
Cytogenetic Analysis:	This is a near diploid line. The modal chromosome number is 47 occurring at 38%, and the rate of polyploidy is 9%. Fifteen to sixteen marker chromosomes are present in all cells. They are t(1,?), t(3p,5q), der(3)t(?q29;?), t(3q,?), 5q+, i(6p), t(7q,?), 9q+, t(10q,21q), 16q+ and five to six others. Normal chromosomes 3, 10, 13 and 16 are absent. There are two copies of the X chromosome. No Y chromosomes were detected in QM stained preparations
Isoenzymes:	ES-D, 1 G6PD, B GLO-I, 2 Me-2, 1 PGM1, 1 PGM3, 0
Age:	1 year
Gender:	female
Ethnicity:	Caucasian
Comments:	The WERI-Rb-1 line is one of two human retinoblastoma cell lines established in 1974 by R.M. McFall and T.W. Sery. The cells survive culturing in Difco Bacto-Agar but do not form colonies. Scanning electron microscopy reveals some variation in the number and frequency of surface blebs, lamellipodia and microvilli. The line is of interest in studies of cell differentiation, animal models of tumor therapy and biochemical evaluations.
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%. Atmosphere: 5% CO2 in air recommended Temperature: 37.0°C
Subculturing:	Protocol: Cultures can be maintained by addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension in fresh medium at 2 - 3 X 10 exp5 viable cells/ml. Maintain cell density between 1 X 10 exp5 and 1 to 2 X 10 exp6 viable cells/ml. Medium Renewal: Every 3 to 4 days
Preservation:	Freeze medium: Complete growth 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 30-2001 recommended serum:ATCC 30-2020
References:	23026: McFall RC, et al. Characterization of a new continuous cell line derived from a human retinoblastoma. Cancer Res. 37: 1003-1010, 1977. PubMed: 844036 23030: McFall RC, et al. Scanning electron microscopic observation of two retinoblastoma cell lines. Cancer Res. 38: 2827-2835, 1978. PubMed:679190 32287: Rostomily RC, et al. Expression of neurogenic basic helix-loop-helix genes in primitive neuroectodermal tumors. Cancer Res. 57: 3526-3531, 1997. PubMed: 9270024

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