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CCD-1059Sk
CCD-1059Sk
规格:
货期:
编号:TS212461
品牌:Testobio
产品名称: CCD-1059Sk
商品货号: TS212461
Organism: Homo sapiens, human
Tissue: skin
Cell Type: fibroblast
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
Biosafety Level: 1

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: normal
Age: 20 years
Gender: female
Ethnicity: Caucasian
Storage Conditions: liquid nitrogen vapor phase
Derivation:
The line was established from skin taken from normal breast tissue removed at biopsy.
Clinical Data:
20 years
female
Caucasian
Comments:
Cells senesce after approximately 35 population doublings.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Eagles 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%.
Subculturing: Volumes used in this protocol are for 75 cm2 flask; 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 0.25% (w/v) Trypsin-0.53mM 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 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.

Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended
Medium Renewal: Every 3 to 4 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

    Cryopreservation: Complete growth medium, 95%; DMSO, 5%
    Culture Conditions:
    Temperature: 37°C
    STR Profile:
    Amelogenin: X
    CSF1PO: 11,12
    D13S317: 12
    D16S539: 9,11
    D5S818: 11
    D7S820: 11,12
    THO1: 9,9.3
    TPOX: 8
    vWA: 16,18
    Isoenzymes:
    G6PD, B
    Population Doubling Capacity: Cells senesce after approximately 35 population doublings.
    首页 > 产品中心 > 微生物培养 > 菌株 > null > CCD-1059Sk

    CCD-1059Sk

    • 货号: TS212461
    • 好评
    询价
    • 品牌 : TESTOBIO
    产品名称: CCD-1059Sk
    商品货号: TS212461
    Organism: Homo sapiens, human
    Tissue: skin
    Cell Type: fibroblast
    Product Format: frozen
    Morphology: fibroblast
    Culture Properties: adherent
    Biosafety Level: 1

    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: normal
    Age: 20 years
    Gender: female
    Ethnicity: Caucasian
    Storage Conditions: liquid nitrogen vapor phase
    Derivation:
    The line was established from skin taken from normal breast tissue removed at biopsy.
    Clinical Data:
    20 years
    female
    Caucasian
    Comments:
    Cells senesce after approximately 35 population doublings.
    Complete Growth Medium: The base medium for this cell line is ATCC-formulated Eagles 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%.
    Subculturing: Volumes used in this protocol are for 75 cm2 flask; 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 0.25% (w/v) Trypsin-0.53mM 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 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
    5. Add appropriate aliquots of the cell suspension to new culture vessels.
    6. Incubate cultures at 37°C.

    Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended
    Medium Renewal: Every 3 to 4 days

    Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

      Cryopreservation: Complete growth medium, 95%; DMSO, 5%
      Culture Conditions:
      Temperature: 37°C
      STR Profile:
      Amelogenin: X
      CSF1PO: 11,12
      D13S317: 12
      D16S539: 9,11
      D5S818: 11
      D7S820: 11,12
      THO1: 9,9.3
      TPOX: 8
      vWA: 16,18
      Isoenzymes:
      G6PD, B
      Population Doubling Capacity: Cells senesce after approximately 35 population doublings.
      合作单位: