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Documentos clave

8505C

NOTE: Both the cell line and DNA from the cell line may be available for this product. Please choose -1VL or VIAL for cells, or -DNA-5UG for DNA, 94090184, human thyroid, Epithelial

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About This Item

Código UNSPSC:
41106514

origen biológico

human thyroid

envase

tube of 5 μg 94090184-DNA-5UG
pkg of vial of cells 94090184-1VL

modo de crecimiento

Adherent

cariotipo

Not specified

morfología

Epithelial

productos

Not specified

receptores

Not specified

técnicas

cell culture | mammalian: suitable

enfermedades relevantes

cancer

Condiciones de envío

dry ice

temp. de almacenamiento

−196°C

Origen línea celular

Human thyroid carcinoma, undifferentiated.

Descripción línea celular

Established from undifferentiated thyroid carcinomas of a 78 year old female patient. Pathologically this primary carcinoma tissue contained residual well differentiated components suggesting well differentiated to undifferentiated carcinoma progression. Tumour suppresser genes p53, Rb, APC and MCC were analysed and sequence analysis confirmed a C:G to G:C transversion at the first base of p53 gene codon 248. Polymerase chain reaction-loss of heterozygosity assays confirmed allelic deletion of p53 gene. Loss of heterozygosity of tumour suppresser genes was not observed.

Aplicación

8505C cell line has been used to study the impact of synthetic manipulation of expression of microRNAs miR-25 and miR-222 in benign and malignant thyroid cells. It has also been used to determine the induction of pluripotency markers by mitogen activated protein kinase (MEK) inhibition.

Medio de cultivo

EMEM (HBSS) + 2mM Glutamine + 1% Non Essential Amino Acids (NEAA) + 10% Foetal Bovine Serum (FBS).

Rutina de subcultivo

Split sub-confluent cultures (70-80%) 1:3 to 1:6 i.e. seeding at 2-4 x 10,000 cells/cm2 using 0.25% trypsin/EDTA; 5% CO2; 37°C. Doubling time is 36 hours. Saturation density at confluency is 1x100,000 cells/cm2.

Otras notas

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Artículos

DNA, RNA, cDNA derived from ECACC mammalian cell lines allow screening for genes or expression patterns to identify lines most suitable for specific research.

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