B6.129P2-Lamp1tm1Psa/Ph

Status

Available to order

EMMA IDEM:08121
Citation informationRRID:IMSR_EM:08121 

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 nameB6.129P2-Lamp1tm1Psa/Ph
Alternative nameLamp1
Strain typeTargeted Mutant Strains : Knock-out
Allele/Transgene symbolLamp1tm1Psa
Gene/Transgene symbolLamp1

Information from provider

ProviderPaul Saftig
Provider affiliationInstitute of Biochemistry, Christian-Albrechts-University Kiel
Genetic informationFor construction of a targeting vector, a 5.3-kbp KpnI DNA restriction fragment of Lamp1 covering exons 2 and 3 was derived from 129Sv phage library and subcloned. The neo expression cassette was inserted as BamHI DNA restriction fragment into a BglII restriction site located in exon 3 of the KpnI fragment (nucleotide position 323 of the Lamp1 cDNA; amino acid 107 of 382). The insertion of the neo cassette introduces a premature translational stop codon into the open reading frame of the Lamp1 gene. Additionally, for negative selection a thymidine kinase cassette was inserted at the 3' site of the KpnI fragment. Linearized vector was introduced into E14.1 ES cells. Correctly targeted clones were injected into C57BL/6J blastocysts.
Phenotypic informationHomozygous:
Homozygous mice do not exhibit gross changes in the phenotype. Focusing on the brain, Lamp1-deficient mice show altered cathepsin D immunoreactivity and mild astrogliosis.

Heterozygous:
Heterozygous animals appear normal, like wild-type animals.
Breeding historyBackcrossed, N=8
References
  • Normal lysosomal morphology and function in LAMP-1-deficient mice.;Andrejewski N, Punnonen E L, Guhde G, Tanaka Y, Lüllmann-Rauch R, Hartmann D, von Figura K, Saftig P, ;1999;The Journal of biological chemistry;274;12692-701; 10212251
Homozygous fertileyes
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreInstitute of Molecular Genetics, Prague, Czech Republic

Disease and phenotype information

IMPC phenotypes (gene matching)
  • abnormal kidney morphology / IMPC
  • increased circulating phosphate level / IMPC
  • small spleen / IMPC
  • increased lymphocyte cell number / IMPC
  • abnormal retina morphology / IMPC
  • small heart / IMPC
  • small kidney / IMPC
  • increased leukocyte cell number / IMPC
  • abnormal heart morphology / IMPC
MGI phenotypes (gene matching)
  • no abnormal phenotype detected / MGI

Literature references

  • Normal lysosomal morphology and function in LAMP-1-deficient mice.;Andrejewski N, Punnonen E L, Guhde G, Tanaka Y, Lüllmann-Rauch R, Hartmann D, von Figura K, Saftig P, ;1999;The Journal of biological chemistry;274;12692-701; 10212251

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Order

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
(Current health report will be provided later)

Material Transfer Agreement (MTA)
Distribution of this strain is subject to a provider MTA. Both signing of the MTA and submission of the online EMMA Mutant Request Form are required before material can be shipped.

EMMA conditions
Legally binding conditions for the transfer

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