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HCC202
HCC202
规格:
货期:
编号:TS212038
品牌:Testobio
产品名称: HCC202
商品货号: TS212038
Organism: Homo sapiens, human
Tissue: breast; mammary gland/duct
Cell Type: Epithelial
Product Format: frozen
Culture Properties: adherent, The line grows as attached medium-sized epithelial cells with some floating cells.
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: TNM stage IIIA, grade 3, primary ductal carcinoma
Age: 82 years
Gender: female
Ethnicity: Caucasian, White
Karyotype: polyploid
Derivation:
The HCC202 cell line was initiated from a primary ductal carcinoma on September 5, 1992, and took 41 months to establish.
Clinical Data:
82 years
Caucasian, White
female
Receptor Expression:
estrogen receptor, negative
progesterone receptor, negative
Oncogene: her2/neu +, p53 -
Genes Expressed:
Epithelial glycoprotein 2 EGP2; cytokeratin 19
Cellular Products:
Epithelial glycoprotein 2 EGP2; cytokeratin 19
Comments:
The tumor was classified as TNM Stage IIIA, grade 3, invasive ductal carcinoma with metastases in 4 out of 19 lymph nodes.

The cells are poorly differentiated.

The cells are positive for expression of Her2-neu, but are negative for expression of p53.

HCC202 is positive for the epithelial cell specific marker Epithelial Glycoprotein 2 (EGP2) and for cytokeratin 19.

The cells are negative for expression of estrogen receptor (ER -) and progesterone receptor (PR -).





Complete Growth Medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, ATCC 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (ATCC 30-2020) 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-0.53 mM EDTA solution to remove all traces of serum that 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

Subculture Ratio: 1:2 to 1:3
Medium Renewal: Every 2 to 3 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:
Culture medium, 95%; DMSO, 5%
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 10
D13S317: 8,9
D16S539: 13
D5S818: 11,13
D7S820: 8,12
THO1: 6
TPOX: 8,9
vWA: 16
Name of Depositor: AF Gazdar, AK Virmani
Deposited As: Homo sapiens
Year of Origin: September 5, 1992
References:

Gazdar AF, et al. Characterization of paired tumor and non-tumor cell lines established from patients with breast cancer. Int. J. Cancer 78: 766-774, 1998. PubMed: 9833771

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HCC202

  • 货号: TS212038
  • 好评
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  • 品牌 : TESTOBIO
产品名称: HCC202
商品货号: TS212038
Organism: Homo sapiens, human
Tissue: breast; mammary gland/duct
Cell Type: Epithelial
Product Format: frozen
Culture Properties: adherent, The line grows as attached medium-sized epithelial cells with some floating cells.
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: TNM stage IIIA, grade 3, primary ductal carcinoma
Age: 82 years
Gender: female
Ethnicity: Caucasian, White
Karyotype: polyploid
Derivation:
The HCC202 cell line was initiated from a primary ductal carcinoma on September 5, 1992, and took 41 months to establish.
Clinical Data:
82 years
Caucasian, White
female
Receptor Expression:
estrogen receptor, negative
progesterone receptor, negative
Oncogene: her2/neu +, p53 -
Genes Expressed:
Epithelial glycoprotein 2 EGP2; cytokeratin 19
Cellular Products:
Epithelial glycoprotein 2 EGP2; cytokeratin 19
Comments:
The tumor was classified as TNM Stage IIIA, grade 3, invasive ductal carcinoma with metastases in 4 out of 19 lymph nodes.

The cells are poorly differentiated.

The cells are positive for expression of Her2-neu, but are negative for expression of p53.

HCC202 is positive for the epithelial cell specific marker Epithelial Glycoprotein 2 (EGP2) and for cytokeratin 19.

The cells are negative for expression of estrogen receptor (ER -) and progesterone receptor (PR -).





Complete Growth Medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, ATCC 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (ATCC 30-2020) 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-0.53 mM EDTA solution to remove all traces of serum that 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

Subculture Ratio: 1:2 to 1:3
Medium Renewal: Every 2 to 3 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:
Culture medium, 95%; DMSO, 5%
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 10
D13S317: 8,9
D16S539: 13
D5S818: 11,13
D7S820: 8,12
THO1: 6
TPOX: 8,9
vWA: 16
Name of Depositor: AF Gazdar, AK Virmani
Deposited As: Homo sapiens
Year of Origin: September 5, 1992
References:

Gazdar AF, et al. Characterization of paired tumor and non-tumor cell lines established from patients with breast cancer. Int. J. Cancer 78: 766-774, 1998. PubMed: 9833771

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