NCI-H2126 Cells

USUSD$550.00*

Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10⁶ cells for adherent lines or 5 × 10⁶ cells for suspension lines (refer to the batch CoA for details).

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cryovial

產品編號： 300639

安全資料表

產品說明書

分析證明書 (CoA)

說明	The NCI-H2126 cell line is derived from a human large cell carcinoma, a subtype of non-small cell lung cancer (NSCLC). Originating from the lung tissue of a male patient, this cell line exhibits characteristics typical of large cell carcinomas, including poorly differentiated, undifferentiated cellular features. It is an important model for understanding the genetic and molecular mechanisms underlying large cell lung cancers and for testing therapeutic agents targeting this NSCLC subtype. Genomic studies on NCI-H2126 have identified frequent allelic losses and chromosomal aberrations, such as deletions on chromosome arms 6q and 13q, which are commonly implicated in tumor suppressor gene inactivation in NSCLC. These genetic alterations contribute to the disruption of key regulatory pathways, including those involved in cell cycle control and apoptosis. The cell line has been employed in comparative studies to distinguish patterns of chromosomal loss across different lung cancer subtypes, enhancing the understanding of NSCLC-specific molecular signatures. NCI-H2126 has also been included in extensive drug screening programs to evaluate its sensitivity and resistance to various chemotherapeutic agents and targeted therapies. The cell line’s genetic profile and its tumorigenic potential in xenograft models make it a valuable resource for preclinical studies focused on the development and refinement of treatments for large cell carcinoma and other forms of NSCLC.
生物體	Human
組織	Lung
疾病	Large cell carcinoma
轉移部位	Pleural effusion
應用	3D cell culture, Cancer research
同義詞	H-2126, NCIH2126, NCI-H2126

年齡	65 years
性別	Male
族裔	European
形態學	Epithelial
生長特性	Adherent

引用	NCI-H2126 (Cytion catalog number 300639)
生物安全等級	2
NCBI_TaxID	9606
Cellosaurus 編號	CVCL_1532

同工酶	AK-1, 1, ES-D, 1-2, G6PD, B, GLO-I, 2, Me-2, 0, PGM1, 1-2, PGM3, 2
致瘤性	Yes, in nude mice
病毒	EBV (Transformant)
倍性狀態	Hypertriploid

培養基	DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a)
營養補充品	Supplement the medium with 5% FBS, 0.005 mg/mL Insulin, 0.01 mg/mL Transferrin, 30nM Sodium selenite, 10 nM Hydrocortisone, 10 nM beta-estradiol
解離試劑	Accutase
傳代培養	Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
冷凍培養基	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.
細胞解凍與培養	Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit. 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. 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. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening. 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. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium. 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. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.
培養環境	37°C, 5% CO₂, humidified atmosphere.
運送條款	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.
儲存條件	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.

不孕症	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.