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SK-PN-DW

94092301

biological source

human nerve

growth mode

Semi-adherent

karyotype

82XXY

morphology

Polygonal

products

Pro-cholecystokinin (Pro-cck)

receptors

Vimentin, P53, anti-MIC2

technique(s)

cell culture | mammalian: suitable

relevant disease(s)

cancer

shipped in

dry ice

storage temp.

−196°C

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This Item
CB_94092305CB_94092302CB_94092304
SK-PN-DW 94092301

SK-PN-DW

SK-N-DZ 94092305

SK-N-DZ

SK-N-AS 94092302

SK-N-AS

SK-N-F1 94092304

SK-N-F1

growth mode

Semi-adherent

growth mode

Adherent

growth mode

Adherent

growth mode

Adherent/aggregates in suspension

karyotype

82XXY

karyotype

44XX, monosomic for 10, 11, 13, 14, 19. Both copies of chromosome 2 missing in each cell.

karyotype

46

karyotype

Aneuploid

morphology

Polygonal

morphology

Neuronal

morphology

Polygonal

morphology

Epithelial-like

products

Pro-cholecystokinin (Pro-cck)

products

p53, moderate MDR-1 expression

products

Not specified

products

Not specified

receptors

Vimentin, P53, anti-MIC2

receptors

Not specified

receptors

Vimentin

receptors

Transferrin receptor

Cell Line Origin

Human primitive neuroectodermal tumour

Cell Line Description

SK-PN-DW has been derived from a male patient with a primitive neuroectodermal tumour that expresses cholecystokinin (cck) RNA and synthesises substantial amounts of pro-cck. SK-PN-DW is able to process the pro-hormone, producing immunoreactive cck-like material plus a peptide that immunochemically and chromatographically resembles intact cck c-terminal extension peptide. Cells have a tendency to float.

Application

Tumour lines should prove useful in understanding the regulation of the cck gene in human neuronal cells and will also provide an in vitro system for investigation of the post translational processing of the cck preprohormone.

DNA Profile

STR-PCR Data: Amelogenin: X
CSF1PO: 12
D13S317: 9
D16S539: 12
D5S818: 13,14
D7S820: 8,14
THO1: 6
TPOX: 8,9
vWA: 16

Culture Medium

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

Subculture Routine

Split sub-confluent cultures (70-80%) 1:3 to 1:6 i.e. seeding at 2-4x10,000 cells/cm2 using 0.25% trypsin or trypsin/EDTA; 5% CO2; 37°C.

Other Notes

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