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Human Subcutaneous Pre-Adipocytes
Tissue
Adipose tissue (subcutaneous)
Disease
Normal

Documents

Human Subcutaneous Pre-Adipocytes

Cell line · Product number 300697

Human Subcutaneous Pre-Adipocytes are primary preadipocytes isolated from human subcutaneous adipose tissue. They can be expanded and differentiated into mat...

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In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description
Human Subcutaneous Pre-Adipocytes are primary preadipocytes isolated from human subcutaneous adipose tissue. They can be expanded and differentiated into mature adipocytes, serving as a model for adipogenesis, metabolism, obesity, and diabetes research.
Tissue
Adipose tissue (subcutaneous)
Disease
Normal
Applications
Adipogenesis and differentiation studies; obesity, metabolism and diabetes research

02Classification

Organism
Human
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
Fibroblast-like (preadipocyte)
Cell type
Preadipocyte
Doubling time
Approximately 48-72 hours

04Identifiers

Citation
Human Subcutaneous Pre-Adipocytes (Cytion catalog number 300697)
NCBI TaxID
9606

05Handling and culture

Culture medium
Preadipocyte Growth Medium
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Growth supplements; serum (FBS) as per medium
Dissociation reagent
Trypsin-EDTA or Accutase
Subculturing
At 70-80% confluence, wash with PBS, detach with Trypsin-EDTA or Accutase, neutralize, centrifuge at 300xg for 3 min, and reseed into fresh medium.
Split ratio
1:2 to 1:3
Seeding density
5 x 10^3 cells/cm2
Fluid renewal
Every 2-3 days
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 200 x g for 5 minutes, carefully discard the supernatant containing freezing medium.

  7. Follow the procedure described under Post-Thaw Recovery

06Quality control and cryopreservation

Freeze medium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
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.