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Reagentes e instrumentos para imunologia, biologia celular e biologia molecular.

MEL-JUSO genomic DNA - 5 microgram

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Referência 300282GD5

Tamanho : 5µg

Contactar o distribuidor local :

Telefone : +1 850 650 7790

Marca : CLS Cell Lines Service

Contactar o distribuidor local :

Telefone : +1 850 650 7790

MEL-JUSO genomic DNA - 5 microgram

MEL-JUSO Cells

Organism	Human
Tissue	Skin
Disease	Cutaneous melanoma
Synonyms	Mel-Juso, Mel Juso, MelJuSo, MELJUSO, JuSo, MEL-Juso, Mel JuSo

Age	58 years
Gender	Female
Ethnicity	European
Growth properties	Adherent

Citation	MEL-JUSO (Cytion catalog number 300282)

Culture Medium	RPMI 1640, w: 2.1 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
Medium supplements	Supplement the medium with 10% FBS
Passaging solution	PBS, 1 mM EDTA
Freeze medium	CM-1 (Cytion catalog number 800100) or CM-ACF (Cytion catalog number 806100)
Handling of cryopreserved cultures	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. Optionally, skip centrifugation but remove any remaining freezing medium after 24 hours. 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.

Sterility	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.