C57BL/6N-Tg(Th-SNCA*)15Ccs/Ieg

Status

Available to order

EMMA IDEM:14608
International strain nameC57BL/6N-Tg(Th-SNCA*)15Ccs/Ieg
Alternative nameC57BL/6N-Tg(Th-Snca15Hlu)
Strain typeTransgenic Strains
Allele/Transgene symbolTg(Th-SNCA*)1.2Ccs,
Gene/Transgene symbolTg(Th-SNCA*)1.2Ccs

Information from provider

ProviderXinran Zhu
Provider affiliationTierphysiologie, Biologie, Ruhr-Universität Bochum
Genetic informationTh-Snca transgenic mice express the human α-synuclein gene with two missense mutations (A53T and A30P) under the direction of the mouse tyrosine hydroxylase promoter.
Phenotypic informationHomozygous:
Transgenic mice were viable, fertile, and showed no gross anatomical or neuronal abnormalities. Dopaminergic neuron (DA) numbers in the substantia nigra and fiber densities and dopamine levels in the striatum were normal. Accumulation of damaged mitochondrion were observed in DA neurons and in glia cells within the region as well.

Heterozygous:
Transgenic mice were viable, fertile, and showed no gross anatomical or neuronal abnormalities.
Breeding historyThe construct was microinjected into fertilized C57BL/6N oocytes and the founder line 15 were bred to C57BL/6N to establish the colony.
References
  • Mono- and double-mutant mouse models of Parkinson's disease display severe mitochondrial damage.;Stichel Christine C, Zhu Xin-Ran, Bader Verian, Linnartz Bettina, Schmidt Saskia, Lübbert Hermann, ;2007;Human molecular genetics;16;2377-93; 17412759
  • Genetic mouse models for Parkinson's disease display severe pathology in glial cell mitochondria.;Schmidt Saskia, Linnartz Bettina, Mendritzki Sonja, Sczepan Teresa, Lübbert Matthias, Stichel Christine C, Lübbert Hermann, ;2011;Human molecular genetics;20;1197-211; 21212098
  • Influence of different promoters on the expression pattern of mutated human alpha-synuclein in transgenic mice.;Maskri Lyutha, Zhu XinRan, Fritzen Sabrina, Kühn Kati, Ullmer Christoph, Engels Peter, Andriske Michael, Stichel Christine C, Lübbert Hermann, ;2004;Neuro-degenerative diseases;1;255-65; 16908976
Homozygous fertileyes
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisednot known

Information from EMMA

Archiving centreHelmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany
Animals used for archivingheterozygous C57BL/6N

Literature references

  • Mono- and double-mutant mouse models of Parkinson's disease display severe mitochondrial damage.;Stichel Christine C, Zhu Xin-Ran, Bader Verian, Linnartz Bettina, Schmidt Saskia, Lübbert Hermann, ;2007;Human molecular genetics;16;2377-93; 17412759
  • Genetic mouse models for Parkinson's disease display severe pathology in glial cell mitochondria.;Schmidt Saskia, Linnartz Bettina, Mendritzki Sonja, Sczepan Teresa, Lübbert Matthias, Stichel Christine C, Lübbert Hermann, ;2011;Human molecular genetics;20;1197-211; 21212098
  • Influence of different promoters on the expression pattern of mutated human alpha-synuclein in transgenic mice.;Maskri Lyutha, Zhu XinRan, Fritzen Sabrina, Kühn Kati, Ullmer Christoph, Engels Peter, Andriske Michael, Stichel Christine C, Lübbert Hermann, ;2004;Neuro-degenerative diseases;1;255-65; 16908976

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Availabilities

Requesting frozen sperm or embryos is generally advisable wherever possible, in order to minimise the shipment of live mice.

  • Frozen sperm. Delivered in 4 weeks (after paperwork in place). €1740*
  • Rederivation of mice from frozen stock, delivery time available upon request . €3880*

Due to the dynamic nature of our processes strain availability may change at short notice. The local repository manager will advise you in these circumstances.

* In addition users have to cover all the shipping costs (including the cost for returning dry-shippers, where applicable).

More details on pricing and delivery times

Practical information

Example health report
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Material Transfer Agreement (MTA)
For this strain no provider MTA is needed. Distribution is based on the EMMA conditions only.

EMMA conditions
Legally binding conditions for the transfer

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