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MDA-MB-330
MDA-MB-330
规格:
货期:
编号:TS211490
品牌:Testobio
产品名称: MDA-MB-330
商品货号: TS211490
Organism: Homo sapiens, human
Tissue: mammary gland; breast; Derived from metastatic site: pleural effusion
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: Infiltrating lobular carcinoma
Age: 43 years
Gender: female
Ethnicity: Caucasian
Applications:
The population exhibited a mixed phenotype when examined by immunofluorescence staining for tubulin, with some cells (type I) having extensive arrays and others (type II) a more diffuse reaction pattern.
Karyotype: modal number = 64 with one marker chromosome
Images:
Clinical Data:
female
Caucasian
43 years
Antigen Expression:
Blood Type A; Rh+
Receptor Expression:
epidermal growth factor (EGF)
Cellular Products:
tubulin; actin
Tumorigenic: No
Effects:
No, in immunosuppressed mice
Yes, in semisolid medium
Comments:
The population exhibited a mixed phenotype when examined by immunofluorescence staining for tubulin, with some cells (type I) having extensive arrays and others (type II) a more diffuse reaction pattern.
Most cells of the line stained positively for actin.
This line grows very slowly (doubling time is 10 to 20 days) and never becomes confluent.
Complete Growth Medium: These cells are grown in Leibovitzs L-15 medium with 2 mM L-glutamine supplemented with:
  • 30 ng/ ml human recombinant EGF
  • 0.016 mg/ml human recombinant insulin
  • 2mM glutathione
  • 20% fetal bovine serum
Do not filter EGF thru 0.22 micron filter.

(Note: The L-15 medium formulation was devised for use in a free gas exchange with atmospheric air. A CO2 and air mixture is detrimental to cells when using this medium for cultivation)


Subculturing:
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: Once per week
Remove medium, add fresh 0.25% trypsin, 0.02% EDTA solution for 1 to 2 minutes, remove trypsin and let the culture sit at 37C until the cells detach. Add fresh medium, aspirate and dispense into new flasks.
Cryopreservation:
Culture medium, 95%; DMSO, 5%
Culture Conditions:
Temperature: 37.0°C
Atmosphere: air, 100%
STR Profile:
Amelogenin: X
CSF1PO: 10
D13S317: 9
D16S539: 9,12
D5S818: 13
D7S820: 10,11
THO1: 8,9.3
TPOX: 8,11
vWA: 14,16
Isoenzymes:
AK-1, 1
ES-D, 1
G6PD, B
GLO-I, 1
PGM1, 1
PGM3, 1
Population Doubling Time: 240 to 480 hrs
Name of Depositor: R Cailleau
Deposited As: Homo sapiens
References:

Brinkley BR, et al. Variations in cell form and cytoskeleton in human breast carcinoma cells in vitro. Cancer Res. 40: 3118-3129, 1980. PubMed: 7000337

Cruciger Q, et al. Morphological, biochemical and chromosomal characterization of breast tumor lines from pleural effusions. In Vitro 12: 331, 1976.

Siciliano MJ, et al. Mutually exclusive genetic signatures of human breast tumor cell lines with a common chromosomal marker. Cancer Res. 39: 919-922, 1979. PubMed: 427779

Cailleau R, et al. Long-term human breast carcinoma cell lines of metastatic origin: preliminary characterization. In Vitro 14: 911-915, 1978. PubMed: 730202

首页 > 产品中心 > 微生物培养 > 菌株 > null > MDA-MB-330

MDA-MB-330

  • 货号: TS211490
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: MDA-MB-330
商品货号: TS211490
Organism: Homo sapiens, human
Tissue: mammary gland; breast; Derived from metastatic site: pleural effusion
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: Infiltrating lobular carcinoma
Age: 43 years
Gender: female
Ethnicity: Caucasian
Applications:
The population exhibited a mixed phenotype when examined by immunofluorescence staining for tubulin, with some cells (type I) having extensive arrays and others (type II) a more diffuse reaction pattern.
Karyotype: modal number = 64 with one marker chromosome
Images:
Clinical Data:
female
Caucasian
43 years
Antigen Expression:
Blood Type A; Rh+
Receptor Expression:
epidermal growth factor (EGF)
Cellular Products:
tubulin; actin
Tumorigenic: No
Effects:
No, in immunosuppressed mice
Yes, in semisolid medium
Comments:
The population exhibited a mixed phenotype when examined by immunofluorescence staining for tubulin, with some cells (type I) having extensive arrays and others (type II) a more diffuse reaction pattern.
Most cells of the line stained positively for actin.
This line grows very slowly (doubling time is 10 to 20 days) and never becomes confluent.
Complete Growth Medium: These cells are grown in Leibovitzs L-15 medium with 2 mM L-glutamine supplemented with:
  • 30 ng/ ml human recombinant EGF
  • 0.016 mg/ml human recombinant insulin
  • 2mM glutathione
  • 20% fetal bovine serum
Do not filter EGF thru 0.22 micron filter.

(Note: The L-15 medium formulation was devised for use in a free gas exchange with atmospheric air. A CO2 and air mixture is detrimental to cells when using this medium for cultivation)


Subculturing:
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: Once per week
Remove medium, add fresh 0.25% trypsin, 0.02% EDTA solution for 1 to 2 minutes, remove trypsin and let the culture sit at 37C until the cells detach. Add fresh medium, aspirate and dispense into new flasks.
Cryopreservation:
Culture medium, 95%; DMSO, 5%
Culture Conditions:
Temperature: 37.0°C
Atmosphere: air, 100%
STR Profile:
Amelogenin: X
CSF1PO: 10
D13S317: 9
D16S539: 9,12
D5S818: 13
D7S820: 10,11
THO1: 8,9.3
TPOX: 8,11
vWA: 14,16
Isoenzymes:
AK-1, 1
ES-D, 1
G6PD, B
GLO-I, 1
PGM1, 1
PGM3, 1
Population Doubling Time: 240 to 480 hrs
Name of Depositor: R Cailleau
Deposited As: Homo sapiens
References:

Brinkley BR, et al. Variations in cell form and cytoskeleton in human breast carcinoma cells in vitro. Cancer Res. 40: 3118-3129, 1980. PubMed: 7000337

Cruciger Q, et al. Morphological, biochemical and chromosomal characterization of breast tumor lines from pleural effusions. In Vitro 12: 331, 1976.

Siciliano MJ, et al. Mutually exclusive genetic signatures of human breast tumor cell lines with a common chromosomal marker. Cancer Res. 39: 919-922, 1979. PubMed: 427779

Cailleau R, et al. Long-term human breast carcinoma cell lines of metastatic origin: preliminary characterization. In Vitro 14: 911-915, 1978. PubMed: 730202

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