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MCF-10-2A
MCF-10-2A
规格:
货期:
编号:TS211499
品牌:Testobio
产品名称: MCF-10-2A
商品货号: TS211499
Organism: Homo sapiens, human
Tissue:
mammary gland; breast
Cell Type: Epithelial
Product Format: frozen
Morphology: epithelial
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: fibrocystic disease
Age: 36 years
Gender: female
Applications: This is a suitable transfection host.
Disclosure: This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC.
Karyotype: modal number = 40 to 43; XX; five marker chromosomes; double minutes
Derivation:
MCA-10-2A was derived from adherent cells in the population.
The line was produced by long term culture in serum free medium with low Ca++ concentration.
This line was established from the same tumor material as MCF 10A (ATCC CRL-10317) and MCF 10F (ATCC CRL-10318).
Clinical Data:
female
Receptor Expression:
epidermal growth factor (EGF); insulin; glucocorticoid
Genes Expressed:
cytokeratin 19
Cellular Products:
cytokeratin 19
Tumorigenic: No
Effects:
No, in immunosuppressed mice
Yes, in semisolid medium
Comments:
The MCF-10-2A cell line is a non-tumorigenic epithelial cell line that does not undergo senescence after exposure to high calcium levels.
The cells are positive for epithelial cytokeratins and milk fat globule antigen.
They exhibit three dimensional growth in collagen, and infrequently form domes in confluent cultures.
Complete Growth Medium: These cells are grown in a 1:1 mixture of Dulbeccos Modified Eagles Medium and Hamx92s F12 medium (DMEM: F12 Medium; ATCC 30-2006).
Supplemented with:
  • 20 ng/ml epidermal growth factor (Do not filter)
  • 100 ng/ml cholera toxin
  • 0.01 mg/ml bovine insulin
  • 500 ng/ml hydrocortisone
  • 5% horse serum
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-0.03% (w/v) 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.xa0
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: Every 2 to 3 days
Cryopreservation:
culture medium 95%; DMSO, 5%
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 10,12
D13S317: 9
D16S539: 11,12
D5S818: 10,13
D7S820: 10,11
THO1: 8
TPOX: 9,11
vWA: 15,17
Name of Depositor: Michigan Cancer Foundation
Deposited As: Homo sapiens
U.S. Patent Number:
References:

Soule H, McGrath CM. Immortal human mammary epithelial cell lines. US Patent 5,026,637 dated Jun 25 1991

Pauley RJ, et al. Immortal human mammary epithelial cell sublines. US Patent 5,206,165 dated Apr 27 1993

Pauley RJ, et al. Immortal human mammary epithelial cell sublines. US Patent 5,238,840 dated Aug 24 1993

Soule HD, McGrath CM. A simplified method for passage and long-term growth of human mammary epithelial cells. In Vitro Cell. Dev. Biol. 22: 6-12, 1986. PubMed: 2418007

Soule HD, et al. Isolation and characterization of a spontaneously immortalized human breast epithelial cell line, MCF-10. Cancer Res. 50: 6075-6086, 1990. PubMed: 1975513

Tait L, et al. Ultrastructural and immunocytochemical characterization of an immortalized human breast epithelial cell line, MCF-10. Cancer Res. 50: 6087-6094, 1990. PubMed: 1697506

首页 > 产品中心 > 微生物培养 > 菌株 > null > MCF-10-2A

MCF-10-2A

  • 货号: TS211499
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: MCF-10-2A
商品货号: TS211499
Organism: Homo sapiens, human
Tissue:
mammary gland; breast
Cell Type: Epithelial
Product Format: frozen
Morphology: epithelial
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: fibrocystic disease
Age: 36 years
Gender: female
Applications: This is a suitable transfection host.
Disclosure: This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC.
Karyotype: modal number = 40 to 43; XX; five marker chromosomes; double minutes
Derivation:
MCA-10-2A was derived from adherent cells in the population.
The line was produced by long term culture in serum free medium with low Ca++ concentration.
This line was established from the same tumor material as MCF 10A (ATCC CRL-10317) and MCF 10F (ATCC CRL-10318).
Clinical Data:
female
Receptor Expression:
epidermal growth factor (EGF); insulin; glucocorticoid
Genes Expressed:
cytokeratin 19
Cellular Products:
cytokeratin 19
Tumorigenic: No
Effects:
No, in immunosuppressed mice
Yes, in semisolid medium
Comments:
The MCF-10-2A cell line is a non-tumorigenic epithelial cell line that does not undergo senescence after exposure to high calcium levels.
The cells are positive for epithelial cytokeratins and milk fat globule antigen.
They exhibit three dimensional growth in collagen, and infrequently form domes in confluent cultures.
Complete Growth Medium: These cells are grown in a 1:1 mixture of Dulbeccos Modified Eagles Medium and Hamx92s F12 medium (DMEM: F12 Medium; ATCC 30-2006).
Supplemented with:
  • 20 ng/ml epidermal growth factor (Do not filter)
  • 100 ng/ml cholera toxin
  • 0.01 mg/ml bovine insulin
  • 500 ng/ml hydrocortisone
  • 5% horse serum
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-0.03% (w/v) 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.xa0
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: Every 2 to 3 days
Cryopreservation:
culture medium 95%; DMSO, 5%
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 10,12
D13S317: 9
D16S539: 11,12
D5S818: 10,13
D7S820: 10,11
THO1: 8
TPOX: 9,11
vWA: 15,17
Name of Depositor: Michigan Cancer Foundation
Deposited As: Homo sapiens
U.S. Patent Number:
References:

Soule H, McGrath CM. Immortal human mammary epithelial cell lines. US Patent 5,026,637 dated Jun 25 1991

Pauley RJ, et al. Immortal human mammary epithelial cell sublines. US Patent 5,206,165 dated Apr 27 1993

Pauley RJ, et al. Immortal human mammary epithelial cell sublines. US Patent 5,238,840 dated Aug 24 1993

Soule HD, McGrath CM. A simplified method for passage and long-term growth of human mammary epithelial cells. In Vitro Cell. Dev. Biol. 22: 6-12, 1986. PubMed: 2418007

Soule HD, et al. Isolation and characterization of a spontaneously immortalized human breast epithelial cell line, MCF-10. Cancer Res. 50: 6075-6086, 1990. PubMed: 1975513

Tait L, et al. Ultrastructural and immunocytochemical characterization of an immortalized human breast epithelial cell line, MCF-10. Cancer Res. 50: 6087-6094, 1990. PubMed: 1697506

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