C57BL/6NTac-Acvr2bem2H/H

Status

Available to order

EMMA IDEM:16098
Citation informationRRID:IMSR_EM:16098 

Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information.

International strain nameC57BL/6NTac-Acvr2bem2H/H
Alternative nameC57BL/6NTac-Acvr2b/H
Strain typeEndonuclease-mediated
Allele/Transgene symbolAcvr2bem2H
Gene/Transgene symbolAcvr2b

Information from provider

Provider Mary Lyon Centre at MRC Harwell
Provider affiliationMary Lyon Centre at MRC Harwell
Genetic informationActivin A and Acivin receptor subunits including Acvr2b play a role in the remyelination of Oligodendrocyte progenitor cells, a process shown to be hampered in the pathogenesis of Multiple Sclerosis. This strain carries floxed critical exons for Acvr2b and can be useful for studying molecular mechanisms involved in remyelination.
Phenotypic informationHomozygous:
no data available

Heterozygous:
no data available
Breeding historyCoisogenic on C57BL/6NTac
ReferencesNone available
Homozygous fertileyes
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom

Disease and phenotype information

IMPC phenotypes (gene matching)
  • preweaning lethality, incomplete penetrance / IMPC
  • polycystic kidney / IMPC
  • abnormal kidney morphology / IMPC
  • enlarged kidney / IMPC
  • preweaning lethality, complete penetrance / IMPC

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Availabilities

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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.

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Practical information

Genotyping protocol

Example health report
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Material Transfer Agreement (MTA)
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