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UWB1.289+BRCA1
UWB1.289+BRCA1
規(guī)格:
價格:
編號:B224800
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱
UWB1.289+BRCA1
商品貨號
B224800
Organism
Homo sapiens, human
Tissue
ovary
培養(yǎng)基
Product Format
frozen
Morphology
epithelial-like
Culture Properties
adherent
Biosafety Level
2 [Cells contain CMV and SV40 vial DNA sequences]

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Disease
ovarian carcinoma
Age
56
Gender
female
Storage Conditions
liquid nitrogen vapor phase
Images
ATCC CRL-2946 micrograph
Derivation
UWB1.289+BRCA1 is a stable cell line derived from UWB1.289 (ATCC CRL-2945), a BRCA1-null human ovarian cancer line, in which wild-type BRCA1 was restored.
Clinical Data
female
Antigen Expression
BRCA1, positive
cytokeratin 7 (CK-7), positive
calretinin, positive
Wilms' tumor protein (WT), positive
Receptor Expression
estrogen, not expressed
progesterone, not expressed
Oncogene
p53
Genes Expressed
p53, cytokeratin 7 (CK-7)
Comments

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. RefDelloRusso, 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

Restoration of wild-type BRCA1 function in these cells partially restores DNA damage responses.

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%.
    • Subculturing
    Volumes used in this protocol are for 75 cm2 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 37°C 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 103 to 7 X 103 viable cells/cm2 is recommended.
    7. Incubate cultures at 37°C. Subculture when cell concentration is between 4 x 104 and 6 x 104 cells/cm2.

    Subcultivation ratio: A subcultivation ratio of 1:4 to 1:6 is recommended.
    Medium renewal: Every 2 to 3 days

    Cryopreservation
    Freeze medium: complete growth medium, 95%; DMSO, 5%
    Storage temperature: liquid nitrogen vapor phase
    Culture Conditions
    Atmosphere: 5% CO2 in air recommended
    Temperature: 37°C
    STR Profile
    D5S818: 13
    D13S317: 9
    D7S820: 7, 10
    D16S539: 12
    vWA: 16, 19
    THO1: 9
    TPOX: 9, 11
    CSF1PO: 11
    Amelogenin: X
    Population Doubling Time
    approximately 36 hours
    Name of Depositor
    E Swisher
    Year of Origin
    2003
    References

    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

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