RD(ICGE-RD,IC-82963)
RD(ICGE-RD,IC-82963)
RD(ICGE-RD,IC-82963)
RD(ICGE-RD,IC-82963)
Catalog No.
Size
Price
IC-82963
10^6
$498.00
IC-82963
10^6
€547.80
Overview
Organism Homo sapiens, human
Tissue muscle
Product Format frozen
Morphology spindle cells and large multinucleated cells
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 rhabdomyosarcoma
Age 7 years
Gender female
Ethnicity Caucasian
Applications
This cell line can be used for the detection of viruses.
Storage Conditions liquid nitrogen vapor phase
Properties
Karyotype unstable within a hyperdiploid bimodal stemline number of 49 and 50. Twenty-two cells had chromosome associations, 15 cells microchromosomes, 2 cells had fragments, 2 cells with breaks, 2 cells with achromatic gaps and 1 cell with a secondary constriction Note: Cytogenetic information is based on initial seed stock at ATCC. Cytogenetic instability has been reported in the literature for some cell lines.


Clinical Data
7 years
Caucasian
female
Genes Expressed myoglobin; myosin ATPase
Cellular Products
myoglobin
myosin ATPase
Virus Susceptibility Human poliovirus 1 
Vesicular stomatitis, Glasgow (Indiana) 
Vesicular stomatitis, Orsay (Indiana) 
Herpes simplex virus 
Vaccinia virus 
Background
Complete Growth Medium The base medium for this cell line is ATCC-formulated Dulbecco''''''''s Modified Eagle''''''''s Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%. 
Subculturing

Volumes used in this protocol are for a 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, 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 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¡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.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: Every 3 to 4 days
Cryopreservation
Freeze medium: Complete growth medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Temperature: 37¡ãC
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