Name of this Object.

ID of this Object.

Object of this Object.

Type of this Object.

Notebook this object belongs to.

List of possible alternative names this model goes by.

The people who created this model.

The American Type Culture Collection (ATCC) identifying number of this cell line.

The species that this cell was originally cultivated from.

Viruses that are known to be carried by this cell line.

The cDNA models that this cell line produces.

The transcript models that this cell line produces.

The model of the contents of this cell when lysed.

The types of tissue that this cell helps comprise.

Specifies the model of sample that will be used if this model is specified to be used in an experiment.

The average diameter of an individual cell.

The average period of time it takes for a population of these cells to double in number during their exponential growth phase in its preferred media.

Indicate the tags (e.g. GFP, Alexa Fluor 488) that the cell contains, which can indicate the presence and amount of particular features or molecules in the cell.

The primary types of cells that are contained within this sample.

The logarithmic concentration of hydrogen ions of a pure sample of this molecule at room temperature and pressure.

The morphological type of the cell line.

The nominal incubation temperature at which this cell line grows.

The recommended liquid media for the growth of the cells.

The recommended solid media for the growth of the cells.

The recommended media for cryopreservation of these cells, often containing additives that protect the cells during freezing.

The default type of cell culture (adherent or suspension) that should be performed when growing these cells. If a cell line can be cultured via an adherent or suspension culture, this is set to the most common cell culture type for the cell line.

The default method by which to thaw cryovials of this cell line.

The default method by which to wash cultures of this cell line.

The default method by which to change the media for cultures of this cell line.

The default method by which to split this cell line.

Indicates if this molecule emits substantial ionizing radiation.

Indicates if a pure sample of this molecule must be handled in a ventilated enclosures.

Indicates if a pure sample of this molecule is easily set aflame at room temperature and pressure.

Indicates if pure samples of this molecule are strong acids (pH <= 2).

Indicates if pure samples of this molecule are strong acids (pH >= 12).

Indicates if pure samples of this molecule can ignite spontaneously upon exposure to air.

Indicates if pure samples of this molecule react spontaneously upon exposure to water.

Indicates if pure samples of this molecule emit fumes spontaneously when exposed to air.

Indicates this molecule is currently banned from usage in the ECL because the facility isn't yet equiped to handle it.

Indicates if pure samples of this molecule become hazardous once they are expired and must be automatically disposed of when they pass their expiration date.

Indicates if special precautions should be taken in handling this molecule, as indicated by the MSDS classification.

Indicates if this molecule may be safely disposed down a standard drain.

Indicates if pure samples of this molecule have a strong odor.

Indicates if an MSDS is required for this molecule.

The PDF of the MSDS (Materials Saftey Data Sheet) of this molecule.

The National Fire Protection Association (NFPA) 704 hazard diamond classification for this molecule.

The Department of Transportation hazard classification for this molecule.

The Biosafety classification for this molecule.

Indicates if this molecule reacts or degrades in the presence of light.

A list of materials that would be damaged if wetted by this molecule.

Indicates if pure samples of this molecule cannot be reliably aspirated or dispensed on an automated liquid handling robot.

The pipetting parameters used to manipulate pure samples of this model.

Indicates if pure samples of this molecule cannot be performed via the ultrasonic distance method due to vapors interfering with the reading.

Reference microscope images exemplifying the typical appearance of this cell line.

The standard curve used to convert turbidity measurements to cell counts. The cell count conversion factor is the slope of the standard curve, which is used to convert turbidity measurements to cell count.

A description of the acquisition parameters used to collect the data to create the GrowthCurve. The method indicates whether the data was collected by absorbance or nephelometry. The instrument model indicates the model of the instrument used to collect the standard curve data. If the method used was Nephelometry, the beam aperture indicates the diameter of the opening allowing the source light to pass through to the sample when the data was collected. If the method used was Nephelometry, the beam intensity indicates the percentage of the total amount of the source light passed through to hit the sample when the data was collected. If the method used was Nephelometry, integration time indicates the amount of time that light was measured to determine turbidity when the data was collected. If the method used was Absorbance, the wavelength indicates the wavelength of light at which the measurements were taken.