宁波泰斯拓生物

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浙江省宁波市镇海区庄市街道兴庄路9号创e慧谷42号楼B幢401室
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HCC1419

货号 TS212067
中文名称 null
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产品名称: HCC1419
商品货号: TS212067
Organism: Homo sapiens, human
Tissue: mammary gland; breast
Cell Type: Epithelial
Product Format: frozen
Morphology: epithelial
Culture Properties: adherent, The line grows as large epithelial attached cells in island-like formation.
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: 42 years
Gender: female
Ethnicity: Hispanic
Storage Conditions: liquid nitrogen vapor temperature
Karyotype: aneuploid
Derivation:
This cell line was initiated on 12/28/94 from a patient who received prior chemotherapy with no previous family history of breast cancer. The line took 9 months to establish.
Clinical Data:
female
Hispanic
42 years
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 5 out of 5 lymph node metastasis.xa0

The cells are poorly differentiated.xa0

The cells overexpress Her2-neu but are negative for expression of p53. HCC1419 is positive for the epithelial cell specific marker epithelial glycoprotein 2 (EGP2) and for cytokeratin 19.xa0

The cells are negative for expression of estrogen receptor (ER) and for expression of 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 mMxa0EDTA 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 10 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: 2 to 3 times a week.
Note:xa0The line grows as large epithelial attached cells in island-like formation.
Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 13 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney,xa05th edition, published byxa0Wiley-Liss, N.Y., 2005.
Cryopreservation:
Freeze medium: Complete growth medium 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor temperature
Culture Conditions:
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 10,12
D13S317: 9,12
D16S539: 11,12
D5S818: 10,12
D7S820: 11
THO1: 6,9.3
TPOX: 8
vWA: 16,17
Name of Depositor: AF Gazdar, AK Virmani
Year of Origin: December 28, 1994
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