Mine otse sisu juurde
ChaGO-k-1
Kude
Metastatic
Haigus
Bronchogenic carcinoma
Sünonüümid
CHAGO-K-1, ChaGo K-1, ChaGo-K1, CHAGOK1, ChaGoK1

Dokumendid

ChaGO-k-1

Cell line · Toote number 305759

€550.00ilma käibemaksu ja saatmiskuludeta

Kohandamine / Soovitused

Laos
Lot
Soovitatav (värskeim partii)
  • CoA
1

01Üldine teave

Kirjeldus

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.

Kude
Metastatic
Haigus
Bronchogenic carcinoma
Rakendused
3D cell culture, Cancer research
Sünonüümid
  • CHAGO-K-1
  • ChaGo K-1
  • ChaGo-K1
  • CHAGOK1
  • ChaGoK1

02Klassifikatsioon

Organism
Inimene
Sugu
Mees
Kasvuvõime
Järgija
Bioloogilise ohutuse tase
1

03Tunnused

Viide
ChaGO-k-1 (Cytion catalog number 305759)
NCBI maksukood
9606
Cellosaurus
CVCL_1121

04Avaldumine ja vastuvõtlikkus

Antigeeni ekspressioon
HCG; human chorionic gonadotropin (alpha subunit only); estradiol; progesterone; mucin (apomucin, MUC-1, MUC-2)
Isoensüümid
AK-1, 1,ES-D, 1,G6PD, B,GLO-I, 1-2,LDH, 5,Me-2, 0,PGM1, 1,PGM3, 1
Mutatsiooniprofiil
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)

05Käsitlemine ja kasvatamine

Inkubatsiooni keskkond

37°C, 5% CO2, humidified atmosphere.

Vedeliku vahetus
2 to 3 times per week
Sulatamine ja kasvatamine
  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.

06Kvaliteedikontroll ja krüokonserveerimine

Viljatus

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.

Külmutuskeskkond
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.
Säilitamistingimused

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.

Tarne- ja kohaletoimetamistingimused

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.

07Annetaja

Doonori vanus
45 years
Etniline kuuluvus
Caucasian

09Toote üksikasjad

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