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RPMI 8866 Cell Line human

95041316, human blood, Lymphoblastoid

Synonym(s):

R8866 Cells, RPMI8866 Cells, Roswell Park Memorial Institute 8866 Cells

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About This Item

UNSPSC Code:
41106514
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Product Name

RPMI 8866 Cell Line human, 95041316, Lymphoblastoid from blood

biological source

human blood

growth mode

Suspension

karyotype

Not specified

morphology

Lymphoblastoid

products

Not specified

receptors

Immunoglobulin E (IgE) binding factor, Calcitonin

technique(s)

cell culture | mammalian: suitable

relevant disease(s)

cancer

shipped in

dry ice

storage temp.

−196°C

Cell Line Origin

Human B lymphocyte

Cell Line Description

RPMI 8866 has been established from the peripheral blood of a 51-year-old American woman with chronic myelogenous leukaemia in May 1966. The B lymphoid cell line expresses a relatively high amount of calcitonin receptors, membrane bound Ig and soluble IgE-binding factor (Fc epsilon RII/CD23).

Application

Receptor studies, binding assays, hormone studies.

DNA Profile

STR-PCR Data: Amelogenin: X
CSF1PO: 11
D13S317: 10,14
D16S539: 11
D5S818: 12
D7S820: 11,12
THO1: 9.3
TPOX: 8,11
vWA: 14,16

Culture Medium

RPMI 1640 + 2mM Glutamine + 10% Foetal Bovine Serum (FBS).

Subculture Routine

To keep the cells in exponential growth maintain cultures between 3-9x100,000 cells/ml; 5% CO2; 37°C. If starting from a frozen ampoule, add thawed cells to a conical based centrifuge tube e.g. 15ml tube. Slowly add 4 ml of culture medium to the tube. Take a sample of the cell suspension, e.g. 200ul, to count cells. Centrifuge the cell suspension at low speed i.e. 100 - 150 x g for a maximum of 5 minutes. Remove medium and re-suspend the cell pellet at a density of 3 - 5 x 100,000 cells/ml in fresh medium containing 10% serum. Incubate flask at 37 C; 5 - 7% CO2. Check daily. Keep flask in a vertical position until the cells reach the exponential phase of growth, this can take up to 7 days.

Other Notes

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Questions

1–8 of 8 Questions  
  1. Could you provide information on product 95041316-1VL, including the doubling time and data sheet details?

    1 answer
    1. The RPMI 8866 cell line datasheet is accessible through the cell line catalogue entry on the website. Our ECACC cell culturists have recommended that this cell line might require up to 7 days to reach the exponential or log phase of the cell cycle. Once it reaches this phase, the doubling time of the cell line is expected to be around 18-24 hours, provided the cells are seeded at the optimal subculture seeding density of between 2-3 x 10^4 cells/ml.

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  2. Why is Vapor Phase Liquid Nitrogen preferred for storage of Cell Line cells?

    1 answer
    1. If ampules are immersed into liquid phase of liquid nitrogen, it increases the risk of the liquid seeping into the vial. This could lead to problems of cross-contamination and increased risk of the ampule exploding when thawed.

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  3. How many Cell Line cells are in the vial?

    1 answer
    1. Each vial of cells contains 2-3 x 106 cells in 1 ml of freezing media. This is in a 1.8 mL ampule.  For exceptionally large cells, counts may decrease. Suspension cells, generally smaller cells, may contain as many as 4-5 x 106 cells/vial to assure optimal viability upon thaw.

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  4. What passage are my Cell Line cells?

    1 answer
    1. If the passage of the cells is known, it is listed on the product page at the HPA website (www.hpacultures.org.uk).

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  5. Are the Cell Line cells tested for viral pathogens?

    1 answer
    1. HPA Cultures does not perform any viral testing on the cell lines.

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  6. What medium should I use when I thaw the Cell Line cells?

    1 answer
    1. The medium for each cell line is listed on the product page. It is specific to each cell line. If not visible on the Sigma-Aldrich website product page, the HPA website also contains the same information (www.hpacultures.org.uk). The product number for the cell line is the same on either site.

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  7. Are my Cell Line cells mycoplasma tested?

    1 answer
    1. ECACC routinely tests all manufactured cell banks for mycoplasma.

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  8. How do I handle Cell Line frozen cells upon arrival?

    1 answer
    1. Upon receipt, frozen ampules should be transferred directly to vapor phase liquid nitrogen without delay (-135°C) or liquid phase liquid nitrogen if vapor phase is not available. DO NOT use a -80°C freezer as an alternative; this will result in loss of viability.

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