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P3x63Ag8.653
Tissue
Hematopoietic
Disease
Myeloma
Synonyms
P3-x63-Ag8.653, P3-x63-Ag8-653, P3-x63-Ag8 653, P3-x63-Ag 8.653, P3-x63Ag8.653, P3-x63.Ag8.653, P3/x63/Ag8.653, P3x63 Ag8.653, P3x63 AG8-653, P3x63-Ag8.653, P3x63-Ag8.653, P3x63 AG 8.653, P3x63Ag8653, P3-x63-Ag8-6-5-3, P3x63Ag8-6-5-3, P3.times.63 Ag8.653, P3.653, x63-Ag 8.6.5.3, x63-AG 8.653, x63-Ag8-653, x63-Ag8.653, x63.Ag8.653, x63Ag8-653, x63Ag8.653, x63AG8.653, P3-653, GM03570, GM3570, GM03570E, NS653

Documents

P3x63Ag8.653

Cell line · Product number 400118

The cells are resistant to 8-azaguanine and are HAT sensitive. They can be used as fusion partners for producing hybridomas. The cells do not secrete immunog...

€430.00excl. tax and shipping

Customization / Recommendations

In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description
The cells are resistant to 8-azaguanine and are HAT sensitive. They can be used as fusion partners for producing hybridomas. The cells do not secrete immunoglobulin. The cells have been reported to be cholesterol auxotroph due to a deficiency in 3-ketosteroid reductase activity.
Tissue
Hematopoietic
Disease
Myeloma
Synonyms
  • P3-x63-Ag8.653
  • P3-x63-Ag8-653
  • P3-x63-Ag8 653
  • P3-x63-Ag 8.653
  • P3-x63Ag8.653
  • P3-x63.Ag8.653
  • P3/x63/Ag8.653
  • P3x63 Ag8.653
  • P3x63 AG8-653
  • P3x63-Ag8.653
  • P3x63-Ag8.653
  • P3x63 AG 8.653
  • P3x63Ag8653
  • P3-x63-Ag8-6-5-3
  • P3x63Ag8-6-5-3
  • P3.times.63 Ag8.653
  • P3.653
  • x63-Ag 8.6.5.3
  • x63-AG 8.653
  • x63-Ag8-653
  • x63-Ag8.653
  • x63.Ag8.653
  • x63Ag8-653
  • x63Ag8.653
  • x63AG8.653
  • P3-653
  • GM03570
  • GM3570
  • GM03570E
  • NS653

02Classification

Organism
Mouse
Sex
Female
Growth properties
Adherent and suspension
Biosafety level
1

03Characteristics

Morphology
Round cells

04Identifiers

Citation
P3x63Ag8.653 (Cytion catalog number 400118)
NCBI TaxID
10090
Cellosaurus
CVCL_4032

05Expression and susceptibility

Viruses
Tested negative for ectromelia virus (mouse pox).

06Handling and culture

Culture medium
RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Supplement the medium with 10% FBS
Dissociation reagent
Accutase
Subculturing
Gather the suspension cells in a 15 ml tube and gently wash the adherent cells with PBS lacking calcium and magnesium (use 3-5 ml for T25 flasks and 5-10 ml for T75 flasks). Apply Accutase (1-2 ml for T25 flasks, 2.5 ml for T75 flasks) ensuring full coverage of the cell layer. Allow the cells to incubate at room temperature for 10 minutes. Following incubation, combine and centrifuge both the suspension and adherent cells. After centrifugation, carefully resuspend the cell pellet and transfer the cell suspension into new flasks containing fresh medium.
Seeding density
Start new cultures at 4 x 105 cells/ml. The cell density should not exceed 2 x 106 cells/ml.
Fluid renewal
Every 3 to 4 days. Collect floating cells, centrifuge and add to the flask together with fresh medium.
Post-thaw recovery
After thawing, plate the cells at 5 x 104 cells/cm2 and allow the cells to recover from the freezing process and to adhere for at least 48 hours.
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

07Quality control and cryopreservation

Sterility

Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods.

To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.

Freeze medium
As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
Storage conditions

For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.

Shipping conditions

Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.

08Donor

Breed / subspecies
BALB/c