SNU-638 Cells

550,00 CAD$*

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

Numéro de produit : 305634

Fiche signalétique

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Certificat d'analyse (CoA)

Description	The SNU-638 cell line is a human gastric carcinoma model established from the ascitic fluid of a male gastric cancer patient. It exhibits poor differentiation and minimal desmoplasia, and in vitro it grows in a mixed pattern with heterogeneous density and poor attachment to the culture substrate. The cells maintain a round to oval contour and display a low nuclear-to-cytoplasmic ratio, with limited development of microvilli. These characteristics reflect features commonly associated with aggressive gastric cancer phenotypes and make the line suitable for studying poorly differentiated gastric adenocarcinomas. At the molecular level, SNU-638 does not harbor mutations in the c-Ki-ras gene but does express high levels of tumor-associated markers such as CA 19-9 and tissue polypeptide antigen (TPA), with absent alpha-fetoprotein (AFP) expression. It also carries a TP53 gene mutation, which is frequently found in gastric cancers and plays a central role in tumorigenesis. Genomic profiling revealed that SNU-638 lacks MET amplification or overexpression, categorizing it as MET-negative with minimal dependency on the MET signaling pathway. This molecular profile makes SNU-638 a valuable control cell line in studies targeting MET or evaluating the efficacy of MET inhibitors in gastric cancer.
Organisme	Human
Tissu	Gastric
Maladie	Adenocarcinoma
Site métastatique	Ascites
Synonymes	SNU638

Âge	48 years
Genre	Male
Origine ethnique	Korean
Morphologie	Epithelial-like
Type de cellule	Epithelial
Propriétés de croissance	Adherent, monolayer

Référence	SNU-638 (Cytion catalog number 305634)
Niveau de biosécurité	1
NCBI_Numéro d'identification fiscale	9606
Cellosaurus - Numéro d'enregistrement	CVCL_0102

Profil mutationnel	Mutation: MET, Simple, p.Asn375Ser (c.1124A>G), Unspecified; Mutation: TP53, Simple, p.Arg282Trp (c.844C>T), Heterozygous

Milieu de culture	RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
Suppléments	Supplement the medium with 10% heat-inactivated FBS
Réactif de dissociation	Accutase
Temps de doublement	25 hours
Repiquage	Remove medium, add fresh 0.25 % trypsin 0.02 % EDTA solution, stand culture flask at 37''''C for 3 to 5 minutes, add culture medium and collect the cells, transfer the medium into 15ml tube, centrifuge, aspirate the medium, resuspend the pellets with culture medium and dispense into the culture flask
Renouvellement des fluides	2 to 3 times per week
Milieu de congélation	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.
Décongélation et culture des cellules	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.
Atmosphère d'incubation	37°C, 5% CO₂, humidified atmosphere.
Conditions d'expédition	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.
Conditions d'entreposage	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.

Stérilité	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.

Numéro de lot	Type de certificat	Date	Numéro de catalogue
305634-031125	Certificat d'analyse	05. Dec. 2025	305634

SNU-638 Cells

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Certificat d'analyse (CoA)