
NZM2
NZM2 is an adherent cell line derived from a 47 year old male with melanoma metastatic to obturator lymph node
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Description
Description: NZM2 is an adherent cell line derived from a 47 year old male with melanoma metastatic to obturator lymph node.
Description Key Words: Human metastatic melanoma
Also Known As: No other names
Organism: Human (Homo sapiens)
Tissue: melanoma metastatic to obturator lymph node
Growth Properties: Adherent
Doubling Time: 70 hours
Morphology: Epithelial
Growth Medium: This cell line was established by the depositor in: Alpha modified Minimum Essential Medium (MEM) supplemented with 5% Foetal Bovine Serum (FBS)”, 5 ug/ml Insulin, 5 ug/ml Transferrin, 5 ng/ml Sodium Selenite (ITS), in an atmosphere of 5%O2, 5%CO2 and 90%N2.
At CellBank Australia it has been cultured in: Alpha modified Minimum Essential Medium (MEM) supplemented with 10% Foetal Bovine Serum (FBS)”, 5 ug/ml Insulin, 5 ug/ml Transferrin, 5 ng/ml Sodium Selenite (ITS), in an atmosphere of 5%CO2.
Resuscitation: Remove protective cryoflex layer around the ampoule prior to thawing. Thaw the ampoule by gently agitating in a 37°C waterbath; thawing should be rapid (around 2 minutes). A centrifugation step to remove the cryoprotectant after thawing is necessary for this cell line.
Subculturing Procedure:
Medium Renewal: 3 times per week.
Subcultivation Ratio: 1:2 – 1:4 Seeding density 1.2 x104cells/cm2. Split subconfluent cultures(70-80%). Harvest the cells using 0.05% Trypsin/EDTA at 37°C for 5 minutes.
Culture Conditions: Incubate the culture at 37°C with 5% CO2.
Cryoprotectant Medium: 10% DMSO + 90% FCS
Handling Procedure for Frozen Cells: Upon receipt, frozen ampoules should be transferred directly to liquid nitrogen storage without delay, if not to be used immediately. Storage at -80°C may result in loss of viability.
Additional Information:
- Wild-type for BRAF, NRAS, TP53, PIK3CA, PTEN
- CDKN2A/B deletion
- Resistant to temozolomide;
- MGMT expressed
- aneuploid 1.77x diploid; chromosome number 71-78.
NZM1 and NZM2 were developed from the same patient whose malignant lymph nodes were excised 4 weeks apart.
Depositor: Professor Bruce Baguley – The University of Auckland, New Zealand
Reference:
Original Reference:
Marshall ES, Matthews JHL, Shaw JHF, Nixon J, Tumewu P, Finlay GJ, Holdaway KM, Baguley BC.
Radiosensitivity testing of human melanoma cell lines: comparison of [3H]-thymidine incorporation and soft agar clonogenic assays.
Eur J Cancer 1994; 30A: 1370-1376.
PubMed 7999427
Cellosaurus: CVCL_D823
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