NCI-H322 cell

SKU:BHC11101699
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Overview
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NCI-H322 cell is a Club cells cell line derived from Caucasian (Male). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Minimally invasive lung adenocarcinoma
Growth Properties Adherent
Tissue Lung
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Catalog no. Size
305839 1 cryovial
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This cell line is available in the U.S. For non-profit users, please sign and submit the Non-Profit Supply Agreement to orders@biohippo.com before placing an order. For commercial users, please complete the CLEAR Form before ordering, as additional usage fees may apply based on the intended use. For further details, please contact orders@biohippo.com. Products ship after the required agreement is completed; typical delivery is 2–3 business days. Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10^6 cells for adherent lines or 5 × 10^6 cells for suspension lines (refer to the batch CoA for details).

Field Specification
Species Human
NCI-H322 is a human non-small cell lung cancer (NSCLC) cell line derived from an adult patient with a bronchioalveolar carcinoma, a histologic subtype of adenocarcinoma. This cell line was established by the NCI-Navy Medical Oncology Branch as part of a comprehensive effort to generate clinically annotated lung cancer models for research and therapeutic development. NCI-H322 exhibits adherent epithelial morphology in vitro and is typically maintained in RPMI-1640 medium supplemented with 10% fetal bovine serum under standard cell culture conditions. Molecular profiling of NCI-H322 reveals that it carries a KRAS mutation, which contributes to oncogenic signaling through the MAPK/ERK and PI3K/AKT pathways. This mutation renders the cell line resistant to EGFR-targeted therapies and makes it suitable for studies focused on KRAS-driven lung adenocarcinoma. Additionally, the line is wild-type for EGFR and TP53, offering a defined genetic context for dissecting KRAS-dependent tumor biology. Its transcriptional and proteomic data have been included in large-scale datasets such as the Cancer Cell Line Encyclopedia (CCLE), where it has contributed to analyses of lineage-specific vulnerabilities and drug response patterns. NCI-H322 has been used extensively in pharmacologic screening and mechanistic studies to explore sensitivity to MEK inhibitors, PI3K pathway inhibitors, and chemotherapeutic agents. Its consistent performance across studies and well-documented mutation profile make it a valuable preclinical model for KRAS-mutant NSCLC, as well as a key reference in efforts to understand tumor heterogeneity and drug resistance in lung adenocarcinoma.

SKU:BHC11101699

Mutational profile: Mutation: TP53, Simple, p.Arg248Leu (c.743G>T), Homozygous (PubMed=1311061, PubMed=1565469, PubMed=10536175, PubMed=20557307).

  • cultureMedium: RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
  • supplements: Supplement the medium with 10% FBS
  • dissociationReagent: Accutase
  • doublingTime: 50
  • freezeMedium: As a cryopreservation medium, 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.

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