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NCI-H1437 Cell Line

General Information
Organism Homo sapiens, human
Cell Line Description NCI-H1437 is a human non-small cell lung cancer (NSCLC) cell line derived from a stage I lung adenocarcinoma specimen obtained from a 60-year-old male patient. These cells exhibit an epithelial morphology, grow as an adherent monolayer under standard culture conditions, and retain key phenotypic characteristics of lung adenocarcinoma. Cytogenetically, the cell line displays an aneuploid karyotype characterized by various numerical and structural chromosomal alterations. At the molecular level, NCI-H1437 harbors mutations in key cancer-associated genes—including the TP53 tumor suppressor gene and MET—while expressing wild-type KRAS and EGFR. Due to its well-defined genomic profile and stable growth characteristics, NCI-H1437 has become a valuable in vitro model for studying lung adenocarcinoma biology, investigating MET kinase signaling pathways, evaluating novel targeted therapies and chemotherapeutic agents, and conducting functional genomic screens.
Tissue Lung
Disease Lung Adenocarcinoma; Non-Small Cell Lung Cancer (NSCLC)
Morphology Epithelial
Gender Male
Age 60 years
Product Format Frozen
Growth Mode Adherent
Biosafety Level 1 (Biosafety classification is based on U.S. Public Health Service Guidelines)
Applications 1. Research on the pathogenesis of non-small cell lung cancer (NSCLC) and the MET signaling pathway;
2. Evaluation and screening of targeted therapies, small-molecule inhibitors, and chemotherapeutic agents;
3. Research on mechanisms underlying lung cancer cell proliferation, apoptosis, and drug resistance;
4. Functional genomic analysis, target validation, and CRISPR/Cas9 screening and validation.
Shipped In Dry ice
Storage Temperature −196°C
Characteristics
Karyotype Aneuploid
Tumorigenic Yes, tumorigenic in immunocompromised (nude) mice
Genetic Profile TP53 mutation; MET mutation; EGFR wild-type; KRAS wild-type
Mycoplasma Test Negative
Culture Conditions and Handling
Subculturing 1. Remove and discard the culture medium.
2. Briefly rinse the cell monolayer with PBS (without Ca2+/Mg2+) to completely remove residual serum.
3. Add 1.0 to 2.0 mL of 0.25% trypsin-0.03% EDTA solution and incubate at 37°C until the cell monolayer detaches (typically 2 to 5 minutes).
4. Add fresh complete growth medium to neutralize the trypsin and gently pipette up and down to prepare a single-cell suspension.
5. Subculture the cell suspension into new culture vessels.
Medium Renewal Every 2 to 3 days
Subcultivation Ratio A split ratio of 1:3 to 1:6 is recommended
Culture Conditions Atmosphere: Air, 95%; CO2, 5%; Temperature: 37°C
Cryopreservation Complete growth medium supplemented with 5% to 10% (v/v) DMSO
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CSC-RO0154 Cas9 Stable Cell Line - NCI-H1437 Inquiry

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* For research use only. Not intended for any clinical use.
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