SW480(ICGE-SW480,IC-84172)
SW480(ICGE-SW480,IC-84172)
SW480(ICGE-SW480,IC-84172)
SW480(ICGE-SW480,IC-84172)
Catalog No.
Size
Price
IC-84172
10^6
$498.00
IC-84172
10^6
€547.80
Overview
Organism Homo sapiens, human
Tissue colon
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 Dukes'''''''''''''''''''''''''''''''' type B, colorectal adenocarcinoma
Age 50 years
Gender male
Ethnicity Caucasian
Applications

This cell line is a suitable transfection host.

This line has a mutation in codon 12 of the ras proto-oncogene, and can be used as a positive control for PCR assays of mutation in this codon.

Storage Conditions liquid nitrogen vapor phase
Properties
Karyotype The stemline chromosome number is hypotriploid and 11-12 marker chromosomes were common. Both double minutes and dicentrics were observed in 8% of each metaphase examined.


Derivation
SW480 was established from a primary adenocarcinoma of the colon.
Clinical Data
50 years
Caucasian
male
Receptor Expression
epidermal growth factor (EGF)
Oncogene myc +; myb + ; ras +; fos +; sis +; p53 +; abl -; ros -; src -
Genes Expressed
carcinoembryonic antigen (CEA) 0.7 ng/10 6 cells/10 days; keratin; transforming growth factor beta,myc +; myb + ; ras +; fos +; sis +; p53 +; abl -; ros -; src -,HLA A2, B8, B17; blood type A; Rh+,The cells are positive for keratin by immunoperoxidase staining.,The line is positive for expression of c-myc, K-ras, H-ras, N-ras, myb, sis and fos oncogenes.
Cellular Products
carcinoembryonic antigen (CEA) 0.7 ng/10 exp6 cells/10 days; keratin; transforming growth factor beta
Tumorigenic Yes. Tumors developed within 21 days at 100% frequency (5/5) in nude mice inoculated subcutaneously with 10(7) cells.
Effects
Yes, in nude mice
Virus Susceptibility Human immunodeficiency virus 1 , Human immunodeficiency virus 1
Comments

A cell line established from a lymph node metastasis taken from the same patient one year later is available (see ATCCCCL-227).

The line is negative for CSAp (CSAp-) and colon antigen 3.

The cells are positive for keratin by immunoperoxidase staining.

There is a G -> A mutation in codon 273 of the p53 gene resulting in an Arg -> His substitution and a C -> T mutation in codon 309 resulting in a Pro -> Ser substitution.

The cells express elevated levels of p53 protein.

The line is positive for expression of c-myc, K-ras, H-ras, N-ras, myb, sis and fos oncogenes.

N-myc oncogene expression was not detected.

Matrilysin, a metalloproteinase associated with tumor invasiveness, is not expressed.

The cells have been reported to produce GM-CSF.

Background
Complete Growth Medium The base medium for this cell line is ATCC-formulated Leibovitz''''''''''''''''''''''''''''''''s L-15 Medium, Catalog No. 30-2008. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

(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
Volumes are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes. Corning® T-75 flasks (catalog #430641) are recommended for subculturing this product.
  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 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¡ãC 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¡ãC. without CO2.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:8 is recommended
Medium Renewal: 1 to 2 times per week
Cryopreservation
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Atmosphere: air, 100%
Temperature: 37¡ãC
InCellGene


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