SH-SY5Y Cell Line human
94030304, human nerve, Neuroblast
Sinônimo(s):
SHSY5Y Cells, SK-SH-SY5Y Cells, SY5Y Cells
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About This Item
Código UNSPSC:
41106514
Produtos recomendados
Nome do produto
SH-SY5Y Cell Line human, 94030304, Neuroblast from neural tissue.
fonte biológica
human nerve
modo de crescimento
Adherent
cariótipo
Not specified
morfologia
Neuroblast
produtos
Not specified
receptores
Not specified
técnica(s)
cell culture | mammalian: suitable
doença(s) relevante(s)
metastasis
Condições de expedição
dry ice
temperatura de armazenamento
−196°C
Origem de linhagem celular
Human neuroblastoma
Descrição de linhagem celular
SH-SY5Y is a thrice-cloned sub-line of bone marrow biopsy-derived line SK-N-SH (Sigma catalogue no. 86012802). SH-SY-5Y has dopamine-β-hydroxylase activity and can convert glutamate to the neurotransmitter GABA. Will form tumours in nude mice in approximately 3-4 weeks. The loss of neuronal characteristics has been described with increasing passage numbers. Therefore it is recommended to verify specific characteristics such as noradrenalin uptake or neuronal markers routinely.
Aplicação
SH-SY5Y cell line human is used for neurotransmitter studies
SH-SY5Y cell line human has been used to:
SH-SY5Y cell line human has been used to:
- study the iron-mediated toxicity of amyloid β peptide
- check the significance of anionic luminescent conjugated polythiophene (LCP) polythiophene acetic acid (PTAA) in vital staining of cells
- study the effect of haloperidol on sigma-1 receptors in guinea pig brain and human neuroblastoma cells
Outras notas
- DNA is stored at -70 °C
- RNA is stored at -70 °C
- Cell line is stored at -196 °C
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Perfil do DNA
STR-PCR Data: Amelogenin: X
CSF1PO: 11
D13S317: 11
D16S539: 8,13
D5S818: 12
D7S820: 7,10
THO1: 7,10
TPOX: 8,11
vWA: 14,18
CSF1PO: 11
D13S317: 11
D16S539: 8,13
D5S818: 12
D7S820: 7,10
THO1: 7,10
TPOX: 8,11
vWA: 14,18
Meio de cultura
Ham′s F12:EMEM (EBSS) (1:1) + 2mM Glutamine + 1% Non Essential Amino AcidsNEAA + 15% Foetal Bovine Serum FBS / FCS.
Rotina de subcultura
Split sub-confluent cultures (70-80%) 1:10 to 1:100 i.e. seeding at 1x1,000-1x10,000 cells/cm2; using 0.25% Trypsin or Trypsin/EDTA, 5% CO2; 37°C. Cells may reattach slowly and may remain in suspension for several days. The loss of neuronal characteristics has been described with increasing passage numbers. Therefore it is recommended to verify specific characteristics such as noradrenalin uptake or neuronal markers routinely.
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