Strain Name:

STOCK Notch1tm2Rko/GridJ

Stock Number:

006951

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Description

The genotypes of the animals provided may not reflect those discussed in the strain description or the mating scheme utilized by The Jackson Laboratory prior to cryopreservation. Please inquire for possible genotypes for this specific strain.

Strain Information

Type Mutant Stock; Targeted Mutation;
Additional information on Genetically Engineered and Mutant Mice.
Visit our online Nomenclature tutorial.
Specieslaboratory mouse
Generation?pN1
Generation Definitions
 
Donating Investigator Raphael Kopan,   Washington University in St. Louis

Description
Mice homozygous for this "floxed" Notch1 allele (fN1) are viable and fertile. In the targeted allele, loxP sites were placed flanking exon 1 of the targeted gene. When these floxed mice are bred to mice expressing Cre recombinase, exon 1 of the targeted gene is deleted in cre-expressing tissue(s) in the cre-positive, homozygous floxed offspring. These conditional knockout mice may be useful in generating tissue-specific mutants for studying the development of a wide range of tissues: for example, when crossed to a strain expressing Cre recombinase primarily in the nervous system (see Stock No. 003771), this mutant strain may be useful in studies of apoptosis in neural development.

When crossed to a strain expressing a differential Cre mediated reporter protein labeling: Notch1 signaling in actively cycling stem/progenitor cells (see Stock No. 006953), this mutant strain may be useful in studies of loss of Notch1 heterozygosity.

When bred to mice carrying Tg(Wnt1-cre)11Rth (Stock No. 009107), Cre recombinase expression in the midbrain and developing neural tube results in postnatal lethality.

Development
A targeting construct was designed to place a loxP-flanked PGK-neo cassette upstream of exon 1 of the targeted gene, as well as a single loxP site in intron 1. The construct was electroporated into 129X1/SvJ-derived RW4 embryonic stem (ES) cells. Correctly targeted ES cells were transiently transfected with a Cre recombinase vector to remove the selection cassette. The resulting ES cells harboring the loxP-flanked exon 1 were injected into blastocysts to generate chimeric mice. Mutant mice were then sent to Dr. Thomas Gridley (The Jackson Laboratory) in 2003 on an unspecified mixed genetic background. These mice were supplied to The Jackson Laboratory Repository in 2007.

Control Information

  Control
   None Available
 
  Considerations for Choosing Controls

Related Strains

Strains carrying   Notch1tm2Rko allele
007181   B6.129X1-Notch1tm2Rko/GridJ
View Strains carrying   Notch1tm2Rko     (1 strain)

Strains carrying other alleles of Notch1
002797   B6.129-Notch1tm1Con/J
003332   C57BL/6-Tg(LckNotch1)9Erob/J
008159   STOCK Gt(ROSA)26Sortm1(Notch1)Dam/J
002445   STOCK Notch1tm1Con/J
006953   STOCK Notch1tm3(cre)Rko/J
View Strains carrying other alleles of Notch1     (5 strains)

Additional Web Information

Introduction to Cre-lox technology

Phenotype

Phenotype Information

View Related Disease (OMIM) Terms

Related Disease (OMIM) Terms provided by MGI
- Potential model based on gene homology relationships. Phenotypic similarity to the human disease has not been tested.
Aortic Valve Disease 1; AOVD1   (NOTCH1)
View Mammalian Phenotype Terms

Mammalian Phenotype Terms provided by MGI
      assigned by genotype

The following phenotype information is associated with a similar, but not exact match to this JAX® Mice strain.

Notch1tm2Rko/Notch1tm3(cre)Rko

        involves: 129X1/SvJ * C57BL/6   (conditional)
  • mortality/aging
  • premature death
    • life expectancy is significantly reduced in mutants (420 days) compared to wild-type (600 days)   (MGI Ref ID J:171829)
  • tumorigenesis
  • increased hemangioma incidence
    • 11/13 mice have hemangiosarcoma/vascular tumors, some of which involve multiple organs including the ovary, testis, skin, lymph node, uterus, and colon; liver is the primary site (82% of mice)   (MGI Ref ID J:171829)
  • vision/eye phenotype
  • abnormal cornea morphology
    • corneal hyperplasia develops by 2-3 months in all animals   (MGI Ref ID J:171829)
    • corneal deposits
      • mice develop corneal plaques by 2-3 months; this increases in severity with age   (MGI Ref ID J:171829)
    • corneal vascularization
      • normal cornea is replaced by a vascularized epidermis-like structure   (MGI Ref ID J:171829)
  • hematopoietic system phenotype
  • abnormal spleen morphology
    • marked expansion of the interfollicular compartments is observed   (MGI Ref ID J:171829)
    • enlarged spleen
      • reactive splenomegaly is observed at post mortem   (MGI Ref ID J:171829)
  • extramedullary hematopoiesis
    • observed in the spleen in granulocytic, erythrocytic, and megakaryocytic lineages with no bias in B/T cell lineages   (MGI Ref ID J:171829)
  • liver/biliary system phenotype
  • abnormal liver morphology
    • liver contains numerous reddened large blood filled spaces consistent with occurrence of vascular tumors   (MGI Ref ID J:171829)
    • abnormal hepatic cord morphology
      • hepatic cords are separated by inflammatory infiltrate   (MGI Ref ID J:171829)
    • abnormal liver parenchyma morphology
      • normal parenchyma is replaced either by solid, hypercellular tissue composed of spindle and epithelioid cells interspersed with many vascular channels or by irregular vascular channels lined by cells with scant-to-moderate eosinophilic cytoplasm and round-to-oval nuclei; nuclei of these cells of endothelial origin were hyperchromatic or contained coarse chromatin   (MGI Ref ID J:171829)
      • abnormal liver lobule morphology
        • liver lobes have irregular contours   (MGI Ref ID J:171829)
        • enlarged liver sinusoidal spaces   (MGI Ref ID J:171829)
    • pale liver
      • on post mortem liver is observed to be pale, with many irregular reddened foci; some patches are almost white   (MGI Ref ID J:171829)
  • liver inflammation
    • dense,chronic inflammatory infiltrates are observed around the bile ducts   (MGI Ref ID J:171829)
  • cardiovascular system phenotype
  • corneal vascularization
    • normal cornea is replaced by a vascularized epidermis-like structure   (MGI Ref ID J:171829)
  • enlarged liver sinusoidal spaces   (MGI Ref ID J:171829)
  • hemoperitoneum
    • observed in 6/7 naturally deceased mice   (MGI Ref ID J:171829)
  • increased angiogenesis
    • increased angiogenesis is observed in the ear   (MGI Ref ID J:171829)
  • immune system phenotype
  • abnormal spleen morphology
    • marked expansion of the interfollicular compartments is observed   (MGI Ref ID J:171829)
    • enlarged spleen
      • reactive splenomegaly is observed at post mortem   (MGI Ref ID J:171829)
  • liver inflammation
    • dense,chronic inflammatory infiltrates are observed around the bile ducts   (MGI Ref ID J:171829)

The following phenotype relates to a compound genotype created using this strain.
Contact JAX® Services jaxservices@jax.org for customized breeding options.

Notch1tm2Rko/Notch1tm2Rko Tg(Nes-cre)1Kln/0

        involves: 129X1/SvJ * C57BL/6J * SJL   (conditional)
  • cellular phenotype
  • abnormal apoptosis
    • at E10 the total number of apoptotic cells and relative percentage of apoptotic cells to progenitor cells in the forebrain-midbrain junction is significantly reduced compared to littermate controls   (MGI Ref ID J:90392)
  • nervous system phenotype
  • increased neuron number
    • the number of postmitotic neurons is increased in the telencephalon at E11.5 - 12.5 compared to littermate controls   (MGI Ref ID J:90392)

Notch1tm2Rko/Notch1tm2Rko Tg(Wnt1-cre)11Rth/0

        involves: 129X1/SvJ * C57BL/6 * CBA   (conditional)
  • mortality/aging
  • complete perinatal lethality
    • mutant mice are not viable and die at birth   (MGI Ref ID J:181120)
  • craniofacial phenotype
  • *normal* craniofacial phenotype
    • normal palate formation   (MGI Ref ID J:181120)
View Research Applications

Research Applications
This mouse can be used to support research in many areas including:

Cell Biology Research
Genes Regulating Growth and Proliferation
Signal Transduction

Developmental Biology Research
Growth Defects

Research Tools
Cell Biology Research
Cre-lox System
      loxP-flanked Sequences
Developmental Biology Research
      Cre-lox System

Genes & Alleles

Gene & Allele Information provided by MGI

 
Allele Symbol Notch1tm2Rko
Allele Name targeted mutation 2, Raphael Kopan
Allele Type Targeted (Conditional ready (e.g. floxed), No functional change)
Common Name(s) N1f; NICD1fl; Notch1flox; Notch1tm1Shn; fN1;
Mutation Made By Raphael Kopan,   Washington University in St. Louis
Strain of Origin129X1/SvJ
ES Cell Line NameRW-4
ES Cell Line Strain129X1/SvJ
Gene Symbol and Name Notch1, notch 1
Chromosome 2
Gene Common Name(s) 9930111A19Rik; Mis6; Motch A; N1; NOTCH; RIKEN cDNA 9930111A19 gene; TAN1; Tan1; hN1; lin-12; translocation-associated Notch;
Molecular Note LoxP were inserted flanking the first coding exon of the gene. An adjacent loxP flanked neomycin cassette was removed by Cre-mediated recombination in ES cells prior to production of chimeric animals. [MGI Ref ID J:90392]

Genotyping

Genotyping Information

Genotyping Protocols

Notch1tm2Rko, Standard PCR


Helpful Links

Genotyping resources and troubleshooting

References

References provided by MGI

Selected Reference(s)

Yang X; Klein R; Tian X; Cheng HT; Kopan R; Shen J. 2004. Notch activation induces apoptosis in neural progenitor cells through a p53-dependent pathway. Dev Biol 269(1):81-94. [PubMed: 15081359]  [MGI Ref ID J:90392]

Additional References

Notch1tm2Rko related

Bai S; Kopan R; Zou W; Hilton MJ; Ong CT; Long F; Ross FP; Teitelbaum SL. 2008. NOTCH1 regulates osteoclastogenesis directly in osteoclast precursors and indirectly via osteoblast lineage cells. J Biol Chem 283(10):6509-18. [PubMed: 18156632]  [MGI Ref ID J:133664]

Boyle SC; Liu Z; Kopan R. 2014. Notch signaling is required for the formation of mesangial cells from a stromal mesenchyme precursor during kidney development. Development 141(2):346-54. [PubMed: 24353058]  [MGI Ref ID J:206586]

Del Barrio MG; Taveira-Marques R; Muroyama Y; Yuk DI; Li S; Wines-Samuelson M; Shen J; Smith HK; Xiang M; Rowitch D; Richardson WD. 2007. A regulatory network involving Foxn4, Mash1 and delta-like 4/Notch1 generates V2a and V2b spinal interneurons from a common progenitor pool. Development 134(19):3427-36. [PubMed: 17728344]  [MGI Ref ID J:128001]

Demehri S ; Kopan R. 2009. Notch signaling in bulge stem cells is not required for selection of hair follicle fate. Development 136(6):891-6. [PubMed: 19211676]  [MGI Ref ID J:146637]

Demehri S; Liu Z; Lee J; Lin MH; Crosby SD; Roberts CJ; Grigsby PW; Miner JH; Farr AG; Kopan R. 2008. Notch-deficient skin induces a lethal systemic B-lymphoproliferative disorder by secreting TSLP, a sentinel for epidermal integrity. PLoS Biol 6(5):e123. [PubMed: 18507503]  [MGI Ref ID J:139386]

Demehri S; Turkoz A; Kopan R. 2009. Epidermal Notch1 loss promotes skin tumorigenesis by impacting the stromal microenvironment. Cancer Cell 16(1):55-66. [PubMed: 19573812]  [MGI Ref ID J:150340]

Demehri S; Turkoz A; Manivasagam S; Yockey LJ; Turkoz M; Kopan R. 2012. Elevated epidermal thymic stromal lymphopoietin levels establish an antitumor environment in the skin. Cancer Cell 22(4):494-505. [PubMed: 23079659]  [MGI Ref ID J:192028]

El-Hashash AH; Turcatel G; Al Alam D; Buckley S; Tokumitsu H; Bellusci S; Warburton D. 2011. Eya1 controls cell polarity, spindle orientation, cell fate and Notch signaling in distal embryonic lung epithelium. Development 138(7):1395-407. [PubMed: 21385765]  [MGI Ref ID J:171504]

El-Hashash AH; Turcatel G; Varma S; Berika M; Al Alam D; Warburton D. 2012. Eya1 protein phosphatase regulates tight junction formation in lung distal epithelium. J Cell Sci 125(Pt 17):4036-48. [PubMed: 22685326]  [MGI Ref ID J:198889]

Elyaman W; Bassil R; Bradshaw EM; Orent W; Lahoud Y; Zhu B; Radtke F; Yagita H; Khoury SJ. 2012. Notch receptors and Smad3 signaling cooperate in the induction of interleukin-9-producing T cells. Immunity 36(4):623-34. [PubMed: 22503540]  [MGI Ref ID J:187328]

Fatima A; Culver A; Culver F; Liu T; Dietz WH; Thomson BR; Hadjantonakis AK; Quaggin SE; Kume T. 2014. Murine Notch1 is required for lymphatic vascular morphogenesis during development. Dev Dyn 243(7):957-64. [PubMed: 24659232]  [MGI Ref ID J:210971]

Hatakeyama J; Wakamatsu Y; Nagafuchi A; Kageyama R; Shigemoto R; Shimamura K. 2014. Cadherin-based adhesions in the apical endfoot are required for active Notch signaling to control neurogenesis in vertebrates. Development 141(8):1671-82. [PubMed: 24715457]  [MGI Ref ID J:208850]

Huang Z; Rivas B; Agoulnik AI. 2013. NOTCH1 gain of function in germ cells causes failure of spermatogenesis in male mice. PLoS One 8(7):e71213. [PubMed: 23936265]  [MGI Ref ID J:204938]

Humphreys R; Zheng W; Prince LS; Qu X; Brown C; Loomes K; Huppert SS; Baldwin S; Goudy S. 2012. Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients. Hum Mol Genet 21(6):1374-83. [PubMed: 22156581]  [MGI Ref ID J:181120]

Huppert SS; Ilagan MX; De Strooper B; Kopan R. 2005. Analysis of Notch Function in Presomitic Mesoderm Suggests a gamma-Secretase-Independent Role for Presenilins in Somite Differentiation. Dev Cell 8(5):677-88. [PubMed: 15866159]  [MGI Ref ID J:98438]

Ishifune C; Maruyama S; Sasaki Y; Yagita H; Hozumi K; Tomita T; Kishihara K; Yasutomo K. 2014. Differentiation of CD11c+CX3CR1+ cells in the small intestine requires Notch signaling. Proc Natl Acad Sci U S A 111(16):5986-91. [PubMed: 24711412]  [MGI Ref ID J:208857]

Kaftanovskaya EM; Feng S; Huang Z; Tan Y; Barbara AM; Kaur S; Truong A; Gorlov IP; Agoulnik AI. 2011. Suppression of insulin-like3 receptor reveals the role of beta-catenin and Notch signaling in gubernaculum development. Mol Endocrinol 25(1):170-83. [PubMed: 21147849]  [MGI Ref ID J:182895]

Kiernan AE; Cordes R; Kopan R; Gossler A; Gridley T. 2005. The Notch ligands DLL1 and JAG2 act synergistically to regulate hair cell development in the mammalian inner ear. Development 132(19):4353-62. [PubMed: 16141228]  [MGI Ref ID J:132241]

Klinakis A; Lobry C; Abdel-Wahab O; Oh P; Haeno H; Buonamici S; van De Walle I; Cathelin S; Trimarchi T; Araldi E; Liu C; Ibrahim S; Beran M; Zavadil J; Efstratiadis A; Taghon T; Michor F; Levine RL; Aifantis I. 2011. A novel tumour-suppressor function for the Notch pathway in myeloid leukaemia. Nature 473(7346):230-3. [PubMed: 21562564]  [MGI Ref ID J:172442]

Krebs LT; Starling C; Chervonsky AV; Gridley T. 2010. Notch1 activation in mice causes arteriovenous malformations phenocopied by ephrinB2 and EphB4 mutants. Genesis 48(3):146-50. [PubMed: 20101599]  [MGI Ref ID J:163061]

Kwon C; Cheng P; King IN; Andersen P; Shenje L; Nigam V; Srivastava D. 2011. Notch post-translationally regulates beta-catenin protein in stem and progenitor cells. Nat Cell Biol 13(10):1244-51. [PubMed: 21841793]  [MGI Ref ID J:176965]

Lee J; Basak JM; Demehri S; Kopan R. 2007. Bi-compartmental communication contributes to the opposite proliferative behavior of Notch1-deficient hair follicle and epidermal keratinocytes. Development 134(15):2795-806. [PubMed: 17611229]  [MGI Ref ID J:124114]

Liu Z; Turkoz A; Jackson EN; Corbo JC; Engelbach JA; Garbow JR; Piwnica-Worms DR; Kopan R. 2011. Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice. J Clin Invest 121(2):800-8. [PubMed: 21266774]  [MGI Ref ID J:171829]

Morimoto M; Nishinakamura R; Saga Y; Kopan R. 2012. Different assemblies of Notch receptors coordinate the distribution of the major bronchial Clara, ciliated and neuroendocrine cells. Development 139(23):4365-73. [PubMed: 23132245]  [MGI Ref ID J:190886]

Movahedan A; Afsharkhamseh N; Sagha HM; Shah JR; Milani BY; Milani FY; Logothetis HD; Chan CC; Djalilian AR. 2013. Loss of Notch1 disrupts the barrier repair in the corneal epithelium. PLoS One 8(7):e69113. [PubMed: 23874882]  [MGI Ref ID J:204394]

Murtomaki A; Uh MK; Choi YK; Kitajewski C; Borisenko V; Kitajewski J; Shawber CJ. 2013. Notch1 functions as a negative regulator of lymphatic endothelial cell differentiation in the venous endothelium. Development 140(11):2365-76. [PubMed: 23615281]  [MGI Ref ID J:198575]

Outtz HH; Tattersall IW; Kofler NM; Steinbach N; Kitajewski J. 2011. Notch1 controls macrophage recruitment and Notch signaling is activated at sites of endothelial cell anastomosis during retinal angiogenesis in mice. Blood 118(12):3436-9. [PubMed: 21795743]  [MGI Ref ID J:177068]

Outtz HH; Wu JK; Wang X; Kitajewski J. 2010. Notch1 deficiency results in decreased inflammation during wound healing and regulates vascular endothelial growth factor receptor-1 and inflammatory cytokine expression in macrophages. J Immunol 185(7):4363-73. [PubMed: 20739676]  [MGI Ref ID J:164219]

Pan Y; Lin MH; Tian X; Cheng HT; Gridley T; Shen J; Kopan R. 2004. gamma-secretase functions through Notch signaling to maintain skin appendages but is not required for their patterning or initial morphogenesis. Dev Cell 7(5):731-43. [PubMed: 15525534]  [MGI Ref ID J:94517]

Pan Y; Liu Z; Shen J; Kopan R. 2005. Notch1 and 2 cooperate in limb ectoderm to receive an early Jagged2 signal regulating interdigital apoptosis. Dev Biol 286(2):472-82. [PubMed: 16169548]  [MGI Ref ID J:103603]

Roderick JE; Gonzalez-Perez G; Kuksin CA; Dongre A; Roberts ER; Srinivasan J; Andrzejewski C Jr; Fauq AH; Golde TE; Miele L; Minter LM. 2013. Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia. J Exp Med 210(7):1311-29. [PubMed: 23733784]  [MGI Ref ID J:201337]

Shi J; Fallahi M; Luo JL; Petrie HT. 2011. Nonoverlapping functions for Notch1 and Notch3 during murine steady-state thymic lymphopoiesis. Blood 118(9):2511-9. [PubMed: 21768299]  [MGI Ref ID J:177089]

Surendran K; Boyle S; Barak H; Kim M; Stomberski C; McCright B; Kopan R. 2010. The contribution of Notch1 to nephron segmentation in the developing kidney is revealed in a sensitized Notch2 background and can be augmented by reducing Mint dosage. Dev Biol 337(2):386-95. [PubMed: 19914235]  [MGI Ref ID J:157258]

Surendran K; Selassie M; Liapis H; Krigman H; Kopan R. 2010. Reduced Notch signaling leads to renal cysts and papillary microadenomas. J Am Soc Nephrol 21(5):819-32. [PubMed: 20378824]  [MGI Ref ID J:185938]

Tu X; Chen J; Lim J; Karner CM; Lee SY; Heisig J; Wiese C; Surendran K; Kopan R; Gessler M; Long F. 2012. Physiological notch signaling maintains bone homeostasis via RBPjk and Hey upstream of NFATc1. PLoS Genet 8(3):e1002577. [PubMed: 22457635]  [MGI Ref ID J:183534]

Wang Y; Wu B; Chamberlain AA; Lui W; Koirala P; Susztak K; Klein D; Taylor V; Zhou B. 2013. Endocardial to myocardial notch-wnt-bmp axis regulates early heart valve development. PLoS One 8(4):e60244. [PubMed: 23560082]  [MGI Ref ID J:199879]

Wei W; Zeve D; Wang X; Du Y; Tang W; Dechow PC; Graff JM; Wan Y. 2011. Osteoclast progenitors reside in the peroxisome proliferator-activated receptor gamma-expressing bone marrow cell population. Mol Cell Biol 31(23):4692-705. [PubMed: 21947280]  [MGI Ref ID J:178880]

Xing Y; Li A; Borok Z; Li C; Minoo P. 2012. NOTCH1 is required for regeneration of Clara cells during repair of airway injury. Stem Cells 30(5):946-55. [PubMed: 22331706]  [MGI Ref ID J:190179]

Zhang Y; Lam O; Nguyen MT; Ng G; Pear WS; Ai W; Wang IJ; Kao WW; Liu CY. 2013. Mastermind-like transcriptional co-activator-mediated Notch signaling is indispensable for maintaining conjunctival epithelial identity. Development 140(3):594-605. [PubMed: 23293291]  [MGI Ref ID J:194073]

Zhao C; Guo H; Li J; Myint T; Pittman W; Yang L; Zhong W; Schwartz RJ; Schwarz JJ; Singer HA; Tallquist MD; Wu M. 2014. Numb family proteins are essential for cardiac morphogenesis and progenitor differentiation. Development 141(2):281-95. [PubMed: 24335256]  [MGI Ref ID J:206589]

Zheng J; Watanabe H; Wines-Samuelson M; Zhao H; Gridley T; Kopan R; Shen J. 2012. Conditional deletion of Notch1 and Notch2 genes in excitatory neurons of postnatal forebrain does not cause neurodegeneration or reduction of Notch mRNAs and proteins. J Biol Chem 287(24):20356-68. [PubMed: 22505716]  [MGI Ref ID J:198896]

Health & husbandry

The genotypes of the animals provided may not reflect those discussed in the strain description or the mating scheme utilized by The Jackson Laboratory prior to cryopreservation. Please inquire for possible genotypes for this specific strain.

Health & Colony Maintenance Information

Animal Health Reports

Production of mice from cryopreserved embryos or sperm occurs in a maximum barrier room, G200.

Colony Maintenance

Breeding & HusbandryWhen maintaining a live colony, homozygous mice are bred.

Pricing and Purchasing

Pricing, Supply Level & Notes, Controls


Pricing for USA, Canada and Mexico shipping destinations View International Pricing

Cryopreserved

Cryopreserved Mice - Ready for Recovery

Price (US dollars $)
Cryorecovery* $2525.00
Animals Provided

At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.

Standard Supply

Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.

Supply Notes

  • Cryorecovery - Standard.
    Progeny testing is not required.

    The average number of mice provided from recovery of our cryopreserved strains is 10. The total number of animals provided, their gender and genotype will vary. We will fulfill your order by providing at least two pair of mice, at least one animal of each pair carrying the mutation of interest. Please inquire if larger numbers of animals with specific genotype and genders are needed. Animals typically ship between 10 and 14 weeks from the date of your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will ship within 25 weeks. IMPORTANT NOTE: The genotypes of animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire about possible genotypes which will be recovered for this specific strain. The Jackson Laboratory cannot guarantee the reproductive success of mice shipped to your facility. If the mice are lost after the first three days (post-arrival) or do not produce progeny at your facility, a new order and fee will be necessary.

    Cryorecovery to establish a Dedicated Supply for greater quantities of mice. Mice recovered can be used to establish a dedicated colony to contractually supply you mice according to your requirements. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 (from U.S.A., Canada or Puerto Rico only) or 1-207-288-5845 (from any location).

Pricing for International shipping destinations View USA Canada and Mexico Pricing

Cryopreserved

Cryopreserved Mice - Ready for Recovery

Price (US dollars $)
Cryorecovery* $3283.00
Animals Provided

At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.

Standard Supply

Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.

Supply Notes

  • Cryorecovery - Standard.
    Progeny testing is not required.

    The average number of mice provided from recovery of our cryopreserved strains is 10. The total number of animals provided, their gender and genotype will vary. We will fulfill your order by providing at least two pair of mice, at least one animal of each pair carrying the mutation of interest. Please inquire if larger numbers of animals with specific genotype and genders are needed. Animals typically ship between 10 and 14 weeks from the date of your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will ship within 25 weeks. IMPORTANT NOTE: The genotypes of animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire about possible genotypes which will be recovered for this specific strain. The Jackson Laboratory cannot guarantee the reproductive success of mice shipped to your facility. If the mice are lost after the first three days (post-arrival) or do not produce progeny at your facility, a new order and fee will be necessary.

    Cryorecovery to establish a Dedicated Supply for greater quantities of mice. Mice recovered can be used to establish a dedicated colony to contractually supply you mice according to your requirements. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 (from U.S.A., Canada or Puerto Rico only) or 1-207-288-5845 (from any location).

View USA Canada and Mexico Pricing View International Pricing

Standard Supply

Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.

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JAX® Mice, Products & Services Conditions of Use

"MICE" means mouse strains, their progeny derived by inbreeding or crossbreeding, unmodified derivatives from mouse strains or their progeny supplied by The Jackson Laboratory ("JACKSON"). "PRODUCTS" means biological materials supplied by JACKSON, and their derivatives. "RECIPIENT" means each recipient of MICE, PRODUCTS, or services provided by JACKSON including each institution, its employees and other researchers under its control. MICE or PRODUCTS shall not be: (i) used for any purpose other than the internal research, (ii) sold or otherwise provided to any third party for any use, or (iii) provided to any agent or other third party to provide breeding or other services. Acceptance of MICE or PRODUCTS from JACKSON shall be deemed as agreement by RECIPIENT to these conditions, and departure from these conditions requires JACKSON's prior written authorization.

No Warranty

MICE, PRODUCTS AND SERVICES ARE PROVIDED “AS IS”. JACKSON EXTENDS NO WARRANTIES OF ANY KIND, EITHER EXPRESS, IMPLIED, OR STATUTORY, WITH RESPECT TO MICE, PRODUCTS OR SERVICES, INCLUDING ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, OR ANY WARRANTY OF NON-INFRINGEMENT OF ANY PATENT, TRADEMARK, OR OTHER INTELLECTUAL PROPERTY RIGHTS.

In case of dissatisfaction for a valid reason and claimed in writing by a purchaser within ninety (90) days of receipt of mice, products or services, JACKSON will, at its option, provide credit or replacement for the mice or product received or the services provided.

No Liability

In no event shall JACKSON, its trustees, directors, officers, employees, and affiliates be liable for any causes of action or damages, including any direct, indirect, special, or consequential damages, arising out of the provision of MICE, PRODUCTS or services, including economic damage or injury to property and lost profits, and including any damage arising from acts or negligence on the part of JACKSON, its agents or employees. Unless prohibited by law, in purchasing or receiving MICE, PRODUCTS or services from JACKSON, purchaser or recipient, or any party claiming by or through them, expressly releases and discharges JACKSON from all such causes of action or damages, and further agrees to defend and indemnify JACKSON from any costs or damages arising out of any third party claims.

MICE and PRODUCTS are to be used in a safe manner and in accordance with all applicable governmental rules and regulations.

The foregoing represents the General Terms and Conditions applicable to JACKSON’s MICE, PRODUCTS or services. In addition, special terms and conditions of sale of certain MICE, PRODUCTS or services may be set forth separately in JACKSON web pages, catalogs, price lists, contracts, and/or other documents, and these special terms and conditions shall also govern the sale of these MICE, PRODUCTS and services by JACKSON, and by its licensees and distributors.

Acceptance of delivery of MICE, PRODUCTS or services shall be deemed agreement to these terms and conditions. No purchase order or other document transmitted by purchaser or recipient that may modify the terms and conditions hereof, shall be in any way binding on JACKSON, and instead the terms and conditions set forth herein, including any special terms and conditions set forth separately, shall govern the sale of MICE, PRODUCTS or services by JACKSON.


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