亚日韩在线中文字幕亚洲,国产在线播放鲁啊鲁视频,张柏芝手扒性器全部图片,亚洲成无码电影在线观看

數(shù)量：大量
器官來源：卵巢
是否是腫瘤細(xì)胞：0
物種來源：人
ATCC Number：CRL-2946?
相關(guān)疾病：其他疾病
細(xì)胞形態(tài)：上皮樣
運(yùn)輸方式：凍存運(yùn)輸
生長狀態(tài)：貼壁生長
年限：56
規(guī)格：0.5ml Designations: UWB1.289+BRCA1
Depositors: ?E. Swisher
Biosafety Level:2
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
Organism: Homo sapiens
Morphology:epithelial-like


Source: Organ: ovary
Disease: ovarian 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.
Isolation: Isolation date: 2003
Receptors:estrogen, not expressed
progesterone, not expressed
Oncogene:p53
Antigen Expression:BRCA1, positive
cytokeratin 7 (CK-7), positive
calretinin, positive
Wilms' tumor protein (WT), positive
DNA Profile (STR):D5S818: 13
D13S317: 9
D7S820: 7, 10
D16S539: 12
vWA: 16, 19
THO1: 9
TPOX: 9, 11
CSF1PO: 11
Amelogenin: X
Age: 56
Gender: female
Comments:UWB1.289+BRCA1 is a stable cell line derived from UWB1.289 (CRL-2945), a BRCA1-null human ovarian cancer line, in which wild-type BRCA1 was restored. A pcDNA3 plasmid carrying wild-type BRCA1 was transfected into the parent line. Restoration of wild-type BRCA1 function in these cells partially restores DNA damage responses. PubMed 17259345.
Propagation: ATCC complete growth medium: The base medium for this cell line is:

50% ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001.

50% MEGM (Mammary Epithelial Growth Medium from Clonetics/Lonza (MEGM Bullet Kit; CC-3150) made of MEBM basal medium and SingleQuot additives (ATCC does not use gentamycin-amphotericin B). Note: Do not filter complete medium. To make the final complete growth medium add the following components to the base medium:

G-418 to a final concentration of 200ug/ml.

fetal bovine serum to a final concentration of 3%.
Atmosphere: 5% CO2 in air recommended
Temperature: 37.0°C

Subculturing: Protocol: Volumes used in this protocol are for 75 sq cm flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.

1. Remove and discard culture medium.
2. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) or 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
3. 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.
4. Add 2.0 to 3.0 ml of complete growth medium and aspirate cells by gently pipetting.
5. Transfer cell suspension to a centrifuge tube and spin at approximately 125 X g for 5 to 10 minutes. Discard supernatant.
6. Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to culture vessels. An inoculum of 5 X 10(3) to 7 X 10(3) viable cells/sq. cm is recommended.
7. Incubate cultures at 37C. Subculture when cell concentration is between 4 X 10(4) and 6 X 10(4) cells/sq. cm.
   Subcultivation ratio: A subcultivation ratio of 1:4 to 1:6 is recommended.
   Medium renewal: Every 2 to 3 days

Preservation: Freeze medium: complete growth medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Doubling Time: approximately 36 hours
Related Products:parental cell line - ATCC CRL-2945 (UWB1.2
Recommended medium: ATCC 30-2001
Recommended serum: ATCC 30-2020
0.25% (w/v) Trypsin - 0.53mM EDTA in Hank's BSS (w/o Ca++, Mg ++): ATCC 30-2101
Phosphate-buffered saline: ATCC 30-2200
Cell culture tested DMSO: ATCC 4-X
Erythrosin B vital stain solution: ATCC 30-2404
References: 16172667: DelloRusso, C., et al. Functional characterization of a novel BRCA1-null ovarian cancer cell line in response to ionizing radiation. Mol Cancer Res.;5(1):35-45, 2007. PubMed 17259345