Ir al contenido
ChaGO-k-1
Pañuelo de papel
Metastatic
Enfermedad
Bronchogenic carcinoma
Sinónimos
CHAGO-K-1, ChaGo K-1, ChaGo-K1, CHAGOK1, ChaGoK1

Documentos

ChaGO-k-1

Cell line · Número de producto 305759

€550.00sin impuestos ni gastos de envío

Personalización / Recomendaciones

En stock
Lote
Recomendado (lote más fresco)
  • CoA
1

01Información general

Descripción

The ChaGo-K-1 cell line is a clonal derivative of the ChaGo human bronchogenic carcinoma line, which was originally established from a primary lung tumor. This subline was developed through single-cell cloning of the parent ChaGo population, specifically selected for its elevated secretion of the α-subunit of human chorionic gonadotropin (HCG-α), a placental glycoprotein hormone subunit that is not typically produced by lung epithelial cells. In detailed hormone profiling, ChaGo-K-1 was shown to secrete extremely high levels of free HCG-α (approximately 290 pmol/day/mg protein), while secreting negligible levels of intact HCG or the β-subunit. This indicates that the cell line ectopically expresses HCG-α in the absence of normal trophoblastic function, a feature characteristic of some tumors exhibiting hormonal dysregulation.

Cytogenetic analysis of ChaGo-K-1 revealed a hyperdiploid karyotype with a modal chromosome number between 51 and 54, indicating chromosomal instability, which is typical of many human cancer cell lines. Importantly, electron microscopy demonstrated no evidence of mycoplasma contamination or viral particles, supporting the cell line’s integrity and suitability for research. The unique ability of ChaGo-K-1 to ectopically secrete HCG-α at levels exceeding even the eutopic secretion of intact HCG by placental tumor cells (e.g., JEG-3) suggests that the mechanisms regulating glycoprotein hormone subunit expression can be co-opted or dysregulated in non-placental malignancies. This property makes ChaGo-K-1 an important model for studying ectopic hormone production, oncogenic dedifferentiation, and tumor-associated glycoprotein signaling.

Pañuelo de papel
Metastatic
Enfermedad
Bronchogenic carcinoma
Aplicaciones
3D cell culture, Cancer research
Sinónimos
  • CHAGO-K-1
  • ChaGo K-1
  • ChaGo-K1
  • CHAGOK1
  • ChaGoK1

02Clasificación

Organismo
Humano
Sexo
Hombre
Propiedades de crecimiento
Adherente
Nivel de bioseguridad
1

03Identificadores

Referencia
ChaGO-k-1 (Cytion catalog number 305759)
N.º de identificación fiscal del NCBI
9606
Cellosaurus
CVCL_1121

04Expresión y susceptibilidad

Expresión de antígenos
HCG; human chorionic gonadotropin (alpha subunit only); estradiol; progesterone; mucin (apomucin, MUC-1, MUC-2)
Isoenzimas
AK-1, 1,ES-D, 1,G6PD, B,GLO-I, 1-2,LDH, 5,Me-2, 0,PGM1, 1,PGM3, 1
Perfil mutacional
Mutation: ARID1A, Simple, c.1921-2A>G, Heterozygous, Note=Splice acceptor mutation (Cosmic-CLP=687596), ARID1A, Simple, p.His684Asp (c.2050C>G), Heterozygous (Cosmic-CLP=687596), RB1, Simple, p.Glu837Lys (c.2509G>A), Homozygous (Cosmic-CLP=687596), TP53, Simple, p.Cys275Phe (c.824G>T), Heterozygous (Cosmic-CLP=687596)

05Manejo y cultivo

Atmósfera de incubación

37°C, 5% CO2, humidified atmosphere.

Renovación de fluidos
2 to 3 times per week
Descongelación y cultivo
  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 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. 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.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

06Control de calidad y criopreservación

Esterilidad

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.

Medio de congelación
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.
Condiciones de almacenamiento

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.

Condiciones de envío

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.

07Donante

Edad del donante
45 years
Origen étnico
Caucasian

09Detalles del producto

Tabla de composición