Strain Name:

B6.129S2-Seletm1Hyn Selptm1Hyn/J

Stock Number:

008437

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Availability:

Cryopreserved - Ready for recovery

Use Restrictions Apply, see Terms of Use
Mice homozygous for both Sele (selectin, endothelial cell) and Selp (selectin, platelet) mutations are viable and fertile. They are characterized by leukocytosis, spontaneous bacterial infections, dermatitis and defective leukocyte recruitment in many models of inflammation.

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 Congenic; Targeted Mutation;
Additional information on Genetically Engineered and Mutant Mice.
Visit our online Nomenclature tutorial.
Additional information on Congenic nomenclature.
Specieslaboratory mouse
 
Donating InvestigatorDr. Richard Hynes,   Massachusetts Institute of Technology

Description
Mice homozygous for both the Seletm1Hyn Selptm1Hyn mutations are viable and fertile. They are characterized by leukocytosis, spontaneous bacterial infections, dermatitis and defective leukocyte recruitment in many models of inflammation.

In an attempt to offer alleles on well-characterized or multiple genetic backgrounds, alleles are frequently moved to a genetic background different from that on which an allele was first characterized. This is the case for the strain above. It should be noted that the phenotype could vary from that originally described. We will modify the strain description if necessary as published results become available.

Development
The Seletm1Hyn mutation was created by replacing the exons encoding the signal peptide, lectin domain, and a portion of the epidermal growth factor domain with a PGK-hygro cassette. To create the Selptm1Hyn mutation, a portion of exon 3 encoding 10 amino acids of a signal peptide and 27 amino acids of the lectin domain was deleted by the insertion of PGK-neo cassette. The two mutations were introduced and selected sequentially in 129S2/SvPas-derived D3 embryonic stem (ES) cells. This line has been backcrossed from a mixed C57BL/6 and 129P2 background to C57BL/6 for more than 10 generations.

Related Strains

View Strains carrying   Seletm1Hyn     (5 strains)

View Strains carrying   Selptm1Hyn     (11 strains)

Strains carrying other alleles of Sele
008238   129S-Seletm1Dmil/J
008434   B6.129S2-Seletm2Hyn/J
008236   B6.129S4-Seletm1Dmil/J
003806   B6;129S-Seletm2Hyn Selltm4Hyn/J
002915   B6;129S2-Seletm2Hyn/J
008435   C.129S2(B6)-Seletm2Hyn/J
008237   C.129S4-Seletm1Dmil/J
View Strains carrying other alleles of Sele     (7 strains)

Strains carrying other alleles of Selp
002285   B6.129S7-Icam1tm1Bay Selptm1Bay/J
002289   B6.129S7-Selptm1Bay/J
View Strains carrying other alleles of Selp     (2 strains)

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.
Hypertension, Essential   (SELE)
IgE Responsiveness, Atopic; IGER   (SELP)
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.

Seletm1Hyn/Seletm1Hyn Selptm1Hyn/Selptm1Hyn

        involves: 129S2/SvPas
  • mortality/aging
  • premature death
    • fatalities are seen in mutants older than 3 months of age that develop bacterial dermatitis   (MGI Ref ID J:31626)
  • hematopoietic system phenotype
  • abnormal hematopoiesis
    • differentiating myeloid precursors are significantly more numerous, however blast forms are not increased, and precursor cells from the erythroid lineage are less numerous in the bone marrow, resulting in a myeloid to erythroid ratio that is increased more than 5-fold   (MGI Ref ID J:31626)
    • abnormal common myeloid progenitor cell morphology
      • spleens contain increased numbers of CFU-GM   (MGI Ref ID J:31626)
    • abnormal erythropoiesis
      • erythropoiesis is partially translocated to the spleen   (MGI Ref ID J:31626)
      • increased erythroid progenitor cell number
        • the number of BFU-E in the spleen are significantly increased   (MGI Ref ID J:31626)
    • abnormal myelopoiesis
      • myeloid precursor are more numerous in the bone marrow   (MGI Ref ID J:31626)
      • the myeloid to erythroid ratio is increased more than 5-fold in these mice   (MGI Ref ID J:31626)
      • abnormal granulocyte differentiation
        • neutrophilic granulocytes compromise most of the cells of the bone marrow with an average of 60% of cells containing the segmented bands and rings morphology as compared to 42% in wild-type mice   (MGI Ref ID J:31626)
    • extramedullary hematopoiesis
      • increased extramedullary hematopoietic activity in the spleen   (MGI Ref ID J:31626)
      • 3 of 10 show evidence of extramedullary hematopoietic activity in the liver   (MGI Ref ID J:31626)
    • impaired hematopoiesis
      • precursor cells of the erythroid lineage are under represented in the bone marrow   (MGI Ref ID J:31626)
    • increased leukocyte cell number
      • there is a 3.9-fold elevation in the mean number of leukocytes in the blood   (MGI Ref ID J:31626)
      • increased eosinophil cell number
        • eosinophil numbers are increased 6.3-fold   (MGI Ref ID J:31626)
      • increased lymphocyte cell number
        • lymphocyte numbers are increased 1.5-fold   (MGI Ref ID J:31626)
      • increased monocyte cell number
        • monocyte numbers are increased 9.8-fold in the blood   (MGI Ref ID J:31626)
      • increased neutrophil cell number
        • more than 16-fold increase in mature polymorphonuclear neutrophils   (MGI Ref ID J:31626)
        • neonates exhibit a 3.3-fold increase in neutrophil numbers   (MGI Ref ID J:31626)
  • abnormal leukocyte tethering or rolling
    • leukocyte rolling along mesenteric venules is virtually absent in these mice   (MGI Ref ID J:31626)
    • TNF pre-treatment leads to a slight increase in rolling though the rolling flux is 46-fold less than in controls   (MGI Ref ID J:31626)
    • the velocity of the rare leukocyte that does bind is much greater than those in wld-type   (MGI Ref ID J:31626)
    • the number of adhering leukocytes is 6-fold less than controls   (MGI Ref ID J:31626)
  • impaired neutrophil recruitment
    • neutrophil recruitment in an induced peritonitis model is reduced   (MGI Ref ID J:31626)
    • there is a five-fold impairment in the number of neutrophils recruited by thioglycollate injection   (MGI Ref ID J:31626)
    • fewer than expected neutrophils are found at the site of skin lesions   (MGI Ref ID J:31626)
  • increased spleen red pulp amount
    • expanded red pulp   (MGI Ref ID J:31626)
  • increased spleen weight
    • splenic weights are increased about 2-fold   (MGI Ref ID J:31626)
  • spleen hyperplasia
    • spleens contain 2-fold more cells   (MGI Ref ID J:31626)
  • immune system phenotype
  • abnormal cytokine level
    • exhibit a 5-fold elevation in GM-CSF levels   (MGI Ref ID J:31626)
    • increased circulating interleukin-3 level
      • mice have 40-fold higher levels of circulating IL-3 than controls   (MGI Ref ID J:31626)
  • abnormal leukocyte tethering or rolling
    • leukocyte rolling along mesenteric venules is virtually absent in these mice   (MGI Ref ID J:31626)
    • TNF pre-treatment leads to a slight increase in rolling though the rolling flux is 46-fold less than in controls   (MGI Ref ID J:31626)
    • the velocity of the rare leukocyte that does bind is much greater than those in wld-type   (MGI Ref ID J:31626)
    • the number of adhering leukocytes is 6-fold less than controls   (MGI Ref ID J:31626)
  • abnormal myelopoiesis
    • myeloid precursor are more numerous in the bone marrow   (MGI Ref ID J:31626)
    • the myeloid to erythroid ratio is increased more than 5-fold in these mice   (MGI Ref ID J:31626)
    • abnormal granulocyte differentiation
      • neutrophilic granulocytes compromise most of the cells of the bone marrow with an average of 60% of cells containing the segmented bands and rings morphology as compared to 42% in wild-type mice   (MGI Ref ID J:31626)
  • impaired neutrophil recruitment
    • neutrophil recruitment in an induced peritonitis model is reduced   (MGI Ref ID J:31626)
    • there is a five-fold impairment in the number of neutrophils recruited by thioglycollate injection   (MGI Ref ID J:31626)
    • fewer than expected neutrophils are found at the site of skin lesions   (MGI Ref ID J:31626)
  • increased leukocyte cell number
    • there is a 3.9-fold elevation in the mean number of leukocytes in the blood   (MGI Ref ID J:31626)
    • increased eosinophil cell number
      • eosinophil numbers are increased 6.3-fold   (MGI Ref ID J:31626)
    • increased lymphocyte cell number
      • lymphocyte numbers are increased 1.5-fold   (MGI Ref ID J:31626)
    • increased monocyte cell number
      • monocyte numbers are increased 9.8-fold in the blood   (MGI Ref ID J:31626)
    • increased neutrophil cell number
      • more than 16-fold increase in mature polymorphonuclear neutrophils   (MGI Ref ID J:31626)
      • neonates exhibit a 3.3-fold increase in neutrophil numbers   (MGI Ref ID J:31626)
  • increased spleen red pulp amount
    • expanded red pulp   (MGI Ref ID J:31626)
  • increased spleen weight
    • splenic weights are increased about 2-fold   (MGI Ref ID J:31626)
  • increased susceptibility to bacterial infection
    • show a high prevalence of spontaneous bacterial dermatitis with or without ulceration, with the majority of mutants 4 months or older developing dermatitis   (MGI Ref ID J:31626)
  • spleen hyperplasia
    • spleens contain 2-fold more cells   (MGI Ref ID J:31626)
  • homeostasis/metabolism phenotype
  • abnormal cytokine level
    • exhibit a 5-fold elevation in GM-CSF levels   (MGI Ref ID J:31626)
    • increased circulating interleukin-3 level
      • mice have 40-fold higher levels of circulating IL-3 than controls   (MGI Ref ID J:31626)
  • cellular phenotype
  • abnormal granulocyte differentiation
    • neutrophilic granulocytes compromise most of the cells of the bone marrow with an average of 60% of cells containing the segmented bands and rings morphology as compared to 42% in wild-type mice   (MGI Ref ID J:31626)
  • abnormal leukocyte tethering or rolling
    • leukocyte rolling along mesenteric venules is virtually absent in these mice   (MGI Ref ID J:31626)
    • TNF pre-treatment leads to a slight increase in rolling though the rolling flux is 46-fold less than in controls   (MGI Ref ID J:31626)
    • the velocity of the rare leukocyte that does bind is much greater than those in wld-type   (MGI Ref ID J:31626)
    • the number of adhering leukocytes is 6-fold less than controls   (MGI Ref ID J:31626)

Seletm1Hyn/Seletm1Hyn Selptm1Hyn/Selptm1Hyn

        involves: 129S2/SvPas * C57BL/6
  • immune system phenotype
  • abnormal leukocyte tethering or rolling
    • rolling leukocytes are virtually absent within the mesenteric venules of mice treated with TNF   (MGI Ref ID J:57973)
    • there is a decrease of about half in the number of adhering leukocytes within these mesenteric venules   (MGI Ref ID J:57973)
    • a population of leukocytes that are "fast rollers" is evident in these mice that are not observed in wild-type mice   (MGI Ref ID J:57973)
  • impaired eosinophil recruitment
    • 2-fold fewer eosinophils are recruited to the peritoneum in response to ragweed allergen challenge   (MGI Ref ID J:57973)
  • impaired neutrophil recruitment
    • neutrophil influx in thioglycollate-induced peritonitis is inhibited at 2, 4, and 8 hours after injection compared to wild-type mice   (MGI Ref ID J:57973)
    • lower numbers of neutrophils are observed than those elicited from mice that are null homozygotes for just one gene   (MGI Ref ID J:57973)
    • numbers of neutrophils increased between 8- 24 hours post injection whereas in wild-type mice they decrease   (MGI Ref ID J:57973)
  • increased leukocyte cell number
    • leukocyte numbers are increased about 50%   (MGI Ref ID J:57973)
    • increased eosinophil cell number
      • eosinophil numbers are about 7-fold higher in the blood   (MGI Ref ID J:57973)
    • increased monocyte cell number
      • monocyte number are increased about 4-fold   (MGI Ref ID J:57973)
    • increased neutrophil cell number
      • neutrophils numbers are increased around 5-fold   (MGI Ref ID J:57973)
  • hematopoietic system phenotype
  • abnormal leukocyte tethering or rolling
    • rolling leukocytes are virtually absent within the mesenteric venules of mice treated with TNF   (MGI Ref ID J:57973)
    • there is a decrease of about half in the number of adhering leukocytes within these mesenteric venules   (MGI Ref ID J:57973)
    • a population of leukocytes that are "fast rollers" is evident in these mice that are not observed in wild-type mice   (MGI Ref ID J:57973)
  • impaired eosinophil recruitment
    • 2-fold fewer eosinophils are recruited to the peritoneum in response to ragweed allergen challenge   (MGI Ref ID J:57973)
  • impaired neutrophil recruitment
    • neutrophil influx in thioglycollate-induced peritonitis is inhibited at 2, 4, and 8 hours after injection compared to wild-type mice   (MGI Ref ID J:57973)
    • lower numbers of neutrophils are observed than those elicited from mice that are null homozygotes for just one gene   (MGI Ref ID J:57973)
    • numbers of neutrophils increased between 8- 24 hours post injection whereas in wild-type mice they decrease   (MGI Ref ID J:57973)
  • increased leukocyte cell number
    • leukocyte numbers are increased about 50%   (MGI Ref ID J:57973)
    • increased eosinophil cell number
      • eosinophil numbers are about 7-fold higher in the blood   (MGI Ref ID J:57973)
    • increased monocyte cell number
      • monocyte number are increased about 4-fold   (MGI Ref ID J:57973)
    • increased neutrophil cell number
      • neutrophils numbers are increased around 5-fold   (MGI Ref ID J:57973)
  • cellular phenotype
  • abnormal leukocyte tethering or rolling
    • rolling leukocytes are virtually absent within the mesenteric venules of mice treated with TNF   (MGI Ref ID J:57973)
    • there is a decrease of about half in the number of adhering leukocytes within these mesenteric venules   (MGI Ref ID J:57973)
    • a population of leukocytes that are "fast rollers" is evident in these mice that are not observed in wild-type mice   (MGI Ref ID J:57973)
View Research Applications

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

Cardiovascular Research
Atherosclerosis
Vascular Defects
      defective leukocyte function

Cell Biology Research
Defects in Cell Adhesion Molecules

Developmental Biology Research
Defects in Cell Adhesion Molecules

Hematological Research
Hematopoietic Defects
Immunological Defects

Immunology, Inflammation and Autoimmunity Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency Associated with Other Defects
Inflammation

Research Tools
Cell Biology Research
Immunology, Inflammation and Autoimmunity Research
Metabolism Research

Seletm1Hyn related

Cardiovascular Research
Atherosclerosis
Vascular Defects
      defective leukocyte function

Cell Biology Research
Defects in Cell Adhesion Molecules

Developmental Biology Research
Defects in Cell Adhesion Molecules

Hematological Research
Hematopoietic Defects
Immunological Defects

Immunology, Inflammation and Autoimmunity Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency Associated with Other Defects
Inflammation

Research Tools
Cell Biology Research
Immunology, Inflammation and Autoimmunity Research
Metabolism Research

Selptm1Hyn related

Immunology, Inflammation and Autoimmunity Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Inflammation

Genes & Alleles

Gene & Allele Information provided by MGI

 
Allele Symbol Seletm1Hyn
Allele Name targeted mutation 1, Richard Hynes
Allele Type Targeted (Null/Knockout)
Common Name(s) E-selectin-; Sele-;
Mutation Made ByDr. Richard Hynes,   Massachusetts Institute of Technology
Strain of Origin129S2/SvPas
ES Cell Line NameD3
ES Cell Line Strain129S2/SvPas
Gene Symbol and Name Sele, selectin, endothelial cell
Chromosome 1
Gene Common Name(s) CD62E; E-selectin; ELAM; ELAM1; ESEL; Elam; LECAM2; endothelial adhesion molecule;
Molecular Note A modified D3 ES cell line heterozygous for the Selptm1Hyn allele was targeted a second time. The exons encoding the signal peptide, lectin domain, and a portion of the epidermal growth factor domain were replaced by the insertion of a PGK-hygro cassette. Both Northern and RT-PCR analysis revealed an absence of normal message for both genes in extracts from cardiac and pulmonary tissue of homozygous mutant mice. This targeted mutation occurred in cis with the Selptm1Hyn mutation. Due to their genomic proximity, the two null alleles should propagate together through the offspring. [MGI Ref ID J:31626]
 
Allele Symbol Selptm1Hyn
Allele Name targeted mutation 1, Richard Hynes
Allele Type Targeted (Null/Knockout)
Common Name(s) P-; P-Selp-; P-selectin-;
Mutation Made ByDr. Richard Hynes,   Massachusetts Institute of Technology
Strain of Origin129S2/SvPas
ES Cell Line NameD3
ES Cell Line Strain129S2/SvPas
Gene Symbol and Name Selp, selectin, platelet
Chromosome 1
Gene Common Name(s) CD62; CD62P; GMP140; GRMP; Grmp; LECAM3; P-selectin; PADGEM; PSEL; PSELECT; granulocyte membrane protein;
Molecular Note A portion of exon 3 encoding 10 amino acids of a signal peptide and 27 amino acids of the lectin domain was replaced with a PGK-neo cassette. Mice were treated with lipopolysaccharide to augment the normally low levels of selectin in lung and liver tissue. A longer transcript, resulting from aberrant or cryptic splicing involving the neomycin cassette, was detected at low levels in mutant mice by Northern blot analysis. RT-PCR further confirmed the presence of low levels of transcript in homozygous mice.Immunofluorescence analysis of activated platelets and lung sections from homozygous mutant mice showed an absence of encoded protein. These results were further confirmed by flow cytometric analysis of activated platelets and metabolic labeling of lung tissue. [MGI Ref ID J:77329]

Genotyping

Genotyping Information

Genotyping Protocols

Seletm1Hyn, Standard PCR
Selptm1Hyn, Standard PCR


Helpful Links

Genotyping resources and troubleshooting

References

References provided by MGI

Selected Reference(s)

Frenette PS; Mayadas TN; Rayburn H; Hynes RO; Wagner DD. 1996. Susceptibility to infection and altered hematopoiesis in mice deficient in both P- and E-selectins. Cell 84(4):563-74. [PubMed: 8598043]  [MGI Ref ID J:31626]

Additional References

Seletm1Hyn related

Doring A; Wild M; Vestweber D; Deutsch U; Engelhardt B. 2007. E- and P-selectin are not required for the development of experimental autoimmune encephalomyelitis in C57BL/6 and SJL mice. J Immunol 179(12):8470-9. [PubMed: 18056394]  [MGI Ref ID J:155033]

Frenette J; Chbinou N; Godbout C; Marsolais D; Frenette PS. 2003. Macrophages, not neutrophils, infiltrate skeletal muscle in mice deficient in P/E selectins after mechanical reloading. Am J Physiol Regul Integr Comp Physiol 285(4):R727-32. [PubMed: 12829442]  [MGI Ref ID J:109393]

Fujita T; Fujimoto M; Matsushita T; Shimada Y; Hasegawa M; Kuwano Y; Ogawa F; Takehara K; Sato S. 2007. Phase-Dependent Roles of E-Selectin during Chronic Contact Hypersensitivity Responses. Am J Pathol 170(5):1649-58. [PubMed: 17456770]  [MGI Ref ID J:121083]

Ghosh S; Chackerian AA; Parker CM; Ballantyne CM; Behar SM. 2006. The LFA-1 adhesion molecule is required for protective immunity during pulmonary Mycobacterium tuberculosis infection. J Immunol 176(8):4914-22. [PubMed: 16585587]  [MGI Ref ID J:131154]

Ginhoux F; Collin MP; Bogunovic M; Abel M; Leboeuf M; Helft J; Ochando J; Kissenpfennig A; Malissen B; Grisotto M; Snoeck H; Randolph G; Merad M. 2007. Blood-derived dermal langerin+ dendritic cells survey the skin in the steady state. J Exp Med 204(13):3133-46. [PubMed: 18086862]  [MGI Ref ID J:130817]

Hidalgo A; Chang J; Jang JE; Peired AJ; Chiang EY; Frenette PS. 2009. Heterotypic interactions enabled by polarized neutrophil microdomains mediate thromboinflammatory injury. Nat Med 15(4):384-91. [PubMed: 19305412]  [MGI Ref ID J:149370]

Hidalgo A; Peired AJ; Wild MK; Vestweber D; Frenette PS. 2007. Complete identification of E-selectin ligands on neutrophils reveals distinct functions of PSGL-1, ESL-1, and CD44. Immunity 26(4):477-89. [PubMed: 17442598]  [MGI Ref ID J:123577]

Hirata T; Furie BC; Furie B. 2002. P-, E-, and L-selectin mediate migration of activated CD8+ T lymphocytes into inflamed skin. J Immunol 169(8):4307-13. [PubMed: 12370362]  [MGI Ref ID J:107382]

Homeister JW; Zhang M; Frenette PS; Hynes RO; Wagner DD; Lowe JB; Marks RM. 1998. Overlapping functions of E- and P-selectin in neutrophil recruitment during acute inflammation. Blood 92(7):2345-52. [PubMed: 9746773]  [MGI Ref ID J:50212]

Ishii T; Fujita T; Matsushita T; Yanaba K; Hasegawa M; Nakashima H; Ogawa F; Shimizu K; Takehara K; Tedder TF; Sato S; Fujimoto M. 2009. Establishment of experimental eosinophilic vasculitis by IgE-mediated cutaneous reverse passive arthus reaction. Am J Pathol 174(6):2225-33. [PubMed: 19389931]  [MGI Ref ID J:148778]

Mendez-Ferrer S; Lucas D; Battista M; Frenette PS. 2008. Haematopoietic stem cell release is regulated by circadian oscillations. Nature 452(7186):442-7. [PubMed: 18256599]  [MGI Ref ID J:134224]

Nacher M; Blazquez AB; Shao B; Matesanz A; Prophete C; Berin MC; Frenette PS; Hidalgo A. 2011. Physiological Contribution of CD44 as a Ligand for E-Selectin during Inflammatory T-Cell Recruitment. Am J Pathol 178(5):2437-46. [PubMed: 21457936]  [MGI Ref ID J:171380]

Oh IY; Yoon CH; Hur J; Kim JH; Kim TY; Lee CS; Park KW; Chae IH; Oh BH; Park YB; Kim HS. 2007. Involvement of E-selectin in recruitment of endothelial progenitor cells and angiogenesis in ischemic muscle. Blood 110(12):3891-9. [PubMed: 17699745]  [MGI Ref ID J:149107]

Papayannopoulou T; Priestley GV; Nakamoto B; Zafiropoulos V; Scott LM. 2001. Molecular pathways in bone marrow homing: dominant role of alpha(4)beta(1) over beta(2)-integrins and selectins. Blood 98(8):2403-11. [PubMed: 11588037]  [MGI Ref ID J:115624]

Robinson SD; Frenette PS; Rayburn H; Cummiskey M; Ullman-Cullere M; Wagner DD; Hynes RO. 1999. Multiple, targeted deficiencies in selectins reveal a predominant role for P-selectin in leukocyte recruitment. Proc Natl Acad Sci U S A 96(20):11452-7. [PubMed: 10500197]  [MGI Ref ID J:57973]

Scheiermann C; Kunisaki Y; Lucas D; Chow A; Jang JE; Zhang D; Hashimoto D; Merad M; Frenette PS. 2012. Adrenergic nerves govern circadian leukocyte recruitment to tissues. Immunity 37(2):290-301. [PubMed: 22863835]  [MGI Ref ID J:187383]

Sobolev O; Stern P; Lacy-Hulbert A; Hynes RO. 2009. Natural killer cells require selectins for suppression of subcutaneous tumors. Cancer Res 69(6):2531-9. [PubMed: 19258505]  [MGI Ref ID J:146885]

Stubke K; Wicklein D; Herich L; Schumacher U; Nehmann N. 2012. Selectin-deficiency reduces the number of spontaneous metastases in a xenograft model of human breast cancer. Cancer Lett 321(1):89-99. [PubMed: 22366582]  [MGI Ref ID J:185633]

Sweeney EA; Priestley GV; Nakamoto B; Collins RG; Beaudet AL; Papayannopoulou T. 2000. Mobilization of stem/progenitor cells by sulfated polysaccharides does not require selectin presence. Proc Natl Acad Sci U S A 97(12):6544-9. [PubMed: 10841555]  [MGI Ref ID J:62722]

Tang T; Frenette PS; Hynes RO; Wagner DD; Mayadas TN. 1996. Cytokine-induced meningitis is dramatically attenuated in mice deficient in endothelial selectins. J Clin Invest 97(11):2485-90. [PubMed: 8647940]  [MGI Ref ID J:107411]

Taverna D; Moher H; Crowley D; Borsig L; Varki A; Hynes RO. 2004. Increased primary tumor growth in mice null for beta3- or beta3/beta5-integrins or selectins. Proc Natl Acad Sci U S A 101(3):763-8. [PubMed: 14718670]  [MGI Ref ID J:88109]

Wicklein D; Schmidt A; Labitzky V; Ullrich S; Valent P; Schumacher U. 2013. E- and p-selectins are essential for repopulation of chronic myelogenous and chronic eosinophilic leukemias in a scid mouse xenograft model. PLoS One 8(7):e70139. [PubMed: 23922938]  [MGI Ref ID J:204363]

Yago T; Fu J; McDaniel JM; Miner JJ; McEver RP; Xia L. 2010. Core 1-derived O-glycans are essential E-selectin ligands on neutrophils. Proc Natl Acad Sci U S A 107(20):9204-9. [PubMed: 20439727]  [MGI Ref ID J:160571]

Zaph C; Scott P. 2003. Th1 cell-mediated resistance to cutaneous infection with Leishmania major is independent of P- and E-selectins. J Immunol 171(9):4726-32. [PubMed: 14568948]  [MGI Ref ID J:107364]

Selptm1Hyn related

Andre P; Denis CV; Ware J; Saffaripour S; Hynes RO; Ruggeri ZM; Wagner DD. 2000. Platelets adhere to and translocate on von willebrand factor presented by endothelium in stimulated veins Blood 96(10):3322-8. [PubMed: 11071623]  [MGI Ref ID J:65812]

Andre P; Hartwell D; Hrachovinova I; Saffaripour S; Wagner DD. 2000. Pro-coagulant state resulting from high levels of soluble P-selectin in blood. Proc Natl Acad Sci U S A 97(25):13835-40. [PubMed: 11095738]  [MGI Ref ID J:125020]

Belanger SD; St-Pierre Y. 2005. Role of selectins in the triggering, growth, and dissemination of T-lymphoma cells: implication of L-selectin in the growth of thymic lymphoma. Blood 105(12):4800-6. [PubMed: 15705798]  [MGI Ref ID J:107461]

Combes V; Rosenkranz AR; Redard M; Pizzolato G; Lepidi H; Vestweber D; Mayadas TN; Grau GE. 2004. Pathogenic role of P-selectin in experimental cerebral malaria: importance of the endothelial compartment. Am J Pathol 164(3):781-6. [PubMed: 14982832]  [MGI Ref ID J:88446]

Connolly ES Jr; Winfree CJ; Prestigiacomo CJ; Kim SC; Choudhri TF; Hoh BL; Naka Y; Solomon RA; Pinsky DJ. 1997. Exacerbation of cerebral injury in mice that express the P-selectin gene: identification of P-selectin blockade as a new target for the treatment of stroke. Circ Res 81(3):304-10. [PubMed: 9285631]  [MGI Ref ID J:43110]

Dole VS; Bergmeier W; Mitchell HA; Eichenberger SC; Wagner DD. 2005. Activated platelets induce Weibel-Palade-body secretion and leukocyte rolling in vivo: role of P-selectin. Blood 106(7):2334-9. [PubMed: 15956287]  [MGI Ref ID J:119376]

Doring A; Wild M; Vestweber D; Deutsch U; Engelhardt B. 2007. E- and P-selectin are not required for the development of experimental autoimmune encephalomyelitis in C57BL/6 and SJL mice. J Immunol 179(12):8470-9. [PubMed: 18056394]  [MGI Ref ID J:155033]

Egami K; Murohara T; Aoki M; Matsuishi T. 2006. Ischemia-induced angiogenesis: role of inflammatory response mediated by P-selectin. J Leukoc Biol 79(5):971-6. [PubMed: 16641139]  [MGI Ref ID J:108660]

Fernekorn U; Butcher EC; Behrends J; Hartz S; Kruse A. 2004. Functional involvement of P-selectin and MAdCAM-1 in the recruitment of alpha4beta7-integrin-expressing monocyte-like cells to the pregnant mouse uterus. Eur J Immunol 34(12):3423-33. [PubMed: 15484189]  [MGI Ref ID J:94597]

Fernekorn U; Butcher EC; Behrends J; Karsten CM; Robke A; Schulze TJ; Kirchner H; Kruse A. 2007. Selectin, platelet plays a critical role in granulocyte access to the pregnant mouse uterus under physiological and pathological conditions. Biol Reprod 76(4):645-53. [PubMed: 17151351]  [MGI Ref ID J:121141]

Forlow SB; White EJ; Barlow SC; Feldman SH; Lu H; Bagby GJ; Beaudet AL; Bullard DC; Ley K. 2000. Severe inflammatory defect and reduced viability in CD18 and E-selectin double-mutant mice J Clin Invest 106(12):1457-66. [PubMed: 11120753]  [MGI Ref ID J:66426]

Frederix K; Chauhan AK; Kisucka J; Zhao BQ; Hoff EI; Spronk HM; Ten Cate H; Wagner DD. 2007. Platelet adhesion receptors do not modulate infarct volume after a photochemically induced stroke in mice. Brain Res 1185:239-45. [PubMed: 17996853]  [MGI Ref ID J:130124]

Frenette J; Chbinou N; Godbout C; Marsolais D; Frenette PS. 2003. Macrophages, not neutrophils, infiltrate skeletal muscle in mice deficient in P/E selectins after mechanical reloading. Am J Physiol Regul Integr Comp Physiol 285(4):R727-32. [PubMed: 12829442]  [MGI Ref ID J:109393]

Ghosh S; Chackerian AA; Parker CM; Ballantyne CM; Behar SM. 2006. The LFA-1 adhesion molecule is required for protective immunity during pulmonary Mycobacterium tuberculosis infection. J Immunol 176(8):4914-22. [PubMed: 16585587]  [MGI Ref ID J:131154]

Ginhoux F; Collin MP; Bogunovic M; Abel M; Leboeuf M; Helft J; Ochando J; Kissenpfennig A; Malissen B; Grisotto M; Snoeck H; Randolph G; Merad M. 2007. Blood-derived dermal langerin+ dendritic cells survey the skin in the steady state. J Exp Med 204(13):3133-46. [PubMed: 18086862]  [MGI Ref ID J:130817]

Gironella M; Molla M; Salas A; Soriano A; Sans M; Closa D; Engel P; Salas A; Pique JM; Panes J. 2002. The role of P-selectin in experimental colitis as determined by antibody immunoblockade and genetically deficient mice. J Leukoc Biol 72(1):56-64. [PubMed: 12101263]  [MGI Ref ID J:124457]

Goerge T; Ho-Tin-Noe B; Carbo C; Benarafa C; Remold-O'Donnell E; Zhao BQ; Cifuni SM; Wagner DD. 2008. Inflammation induces hemorrhage in thrombocytopenia. Blood 111(10):4958-64. [PubMed: 18256319]  [MGI Ref ID J:135316]

Hara T; Shimizu K; Ogawa F; Yanaba K; Iwata Y; Muroi E; Takenaka M; Komura K; Hasegawa M; Fujimoto M; Sato S. 2010. Platelets control leukocyte recruitment in a murine model of cutaneous arthus reaction. Am J Pathol 176(1):259-69. [PubMed: 20008131]  [MGI Ref ID J:156487]

Hidalgo A; Chang J; Jang JE; Peired AJ; Chiang EY; Frenette PS. 2009. Heterotypic interactions enabled by polarized neutrophil microdomains mediate thromboinflammatory injury. Nat Med 15(4):384-91. [PubMed: 19305412]  [MGI Ref ID J:149370]

Hirata T; Furie BC; Furie B. 2002. P-, E-, and L-selectin mediate migration of activated CD8+ T lymphocytes into inflamed skin. J Immunol 169(8):4307-13. [PubMed: 12370362]  [MGI Ref ID J:107382]

Homeister JW; Zhang M; Frenette PS; Hynes RO; Wagner DD; Lowe JB; Marks RM. 1998. Overlapping functions of E- and P-selectin in neutrophil recruitment during acute inflammation. Blood 92(7):2345-52. [PubMed: 9746773]  [MGI Ref ID J:50212]

Horie Y; Wolf R; Anderson DC; Granger DN. 1997. Hepatic leukostasis and hypoxic stress in adhesion molecule-deficient mice after gut ischemia/reperfusion. J Clin Invest 99(4):781-8. [PubMed: 9045883]  [MGI Ref ID J:39161]

Huang HS; Sun DS; Lien TS; Chang HH. 2010. Dendritic cells modulate platelet activity in IVIg-mediated amelioration of ITP in mice. Blood 116(23):5002-9. [PubMed: 20699442]  [MGI Ref ID J:167263]

Johnson RC; Mayadas TN; Frenette PS; Mebius RE; Subramaniam M; Lacasce A; Hynes RO; Wagner DD. 1995. Blood cell dynamics in P-selectin-deficient mice. Blood 86(3):1106-14. [PubMed: 7542495]  [MGI Ref ID J:28190]

Kaifi JT; Hall LR; Diaz C; Sypek J; Diaconu E; Lass JH; Pearlman E. 2000. Impaired eosinophil recruitment to the cornea in P-selectin-deficient mice in onchocerca volvulus keratitis (River blindness) Invest Ophthalmol Vis Sci 41(12):3856-61. [PubMed: 11053286]  [MGI Ref ID J:65551]

Karsten CM; Behrends J; Wagner AK; Fuchs F; Figge J; Schmudde I; Hellberg L; Kruse A. 2009. DC within the pregnant mouse uterus influence growth and functional properties of uterine NK cells. Eur J Immunol 39(8):2203-14. [PubMed: 19593769]  [MGI Ref ID J:151694]

Lu SX; Holland AM; Na IK; Terwey TH; Alpdogan O; Bautista JL; Smith OM; Suh D; King C; Kochman A; Hubbard VM; Rao UK; Yim N; Liu C; Laga AC; Murphy G; Jenq RR; Zakrzewski JL; Penack O; Dykstra L; Bampoe K; Perez L; Furie B; Furie B; van den Brink MR. 2010. Absence of P-selectin in recipients of allogeneic bone marrow transplantation ameliorates experimental graft-versus-host disease. J Immunol 185(3):1912-9. [PubMed: 20622117]  [MGI Ref ID J:162237]

Massaguer A; Perez-Del-Pulgar S; Engel P; Serratosa J; Bosch J; Pizcueta P. 2002. Concanavalin-A-induced liver injury is severely impaired in mice deficient in P-selectin. J Leukoc Biol 72(2):262-70. [PubMed: 12149416]  [MGI Ref ID J:124455]

Mayadas TN. 1995. Gene knockout on p-selectin: its biology and function. Trends Cardiovasc Med 5(4):149-157.  [MGI Ref ID J:28867]

Mayadas TN; Johnson RC; Rayburn H; Hynes RO; Wagner DD. 1993. Leukocyte rolling and extravasation are severely compromised in P selectin-deficient mice. Cell 74(3):541-54. [PubMed: 7688665]  [MGI Ref ID J:77329]

Mayadas TN; Mendrick DL; Brady HR; Tang T; Papayianni A; Assmann KJ; Wagner DD; Hynes RO; Cotran RS. 1996. Acute passive anti-glomerular basement membrane nephritis in P-selectin-deficient mice. Kidney Int 49(5):1342-9. [PubMed: 8731099]  [MGI Ref ID J:113194]

McCafferty DM; Kanwar S; Granger DN; Kubes P. 2000. E/P-selectin-deficient mice: an optimal mutation for abrogating antigen but not tumor necrosis factor-alpha-induced immune responses Eur J Immunol 30(8):2362-71. [PubMed: 10940927]  [MGI Ref ID J:63951]

McCafferty DM; Smith CW; Granger DN; Kubes P. 1999. Intestinal inflammation in adhesion molecule-deficient mice: an assessment of P-selectin alone and in combination with ICAM-1 or E-selectin. J Leukoc Biol 66(1):67-74. [PubMed: 10410991]  [MGI Ref ID J:56590]

Mendez-Ferrer S; Lucas D; Battista M; Frenette PS. 2008. Haematopoietic stem cell release is regulated by circadian oscillations. Nature 452(7186):442-7. [PubMed: 18256599]  [MGI Ref ID J:134224]

Nacher M; Blazquez AB; Shao B; Matesanz A; Prophete C; Berin MC; Frenette PS; Hidalgo A. 2011. Physiological Contribution of CD44 as a Ligand for E-Selectin during Inflammatory T-Cell Recruitment. Am J Pathol 178(5):2437-46. [PubMed: 21457936]  [MGI Ref ID J:171380]

Papayannopoulou T; Priestley GV; Nakamoto B; Zafiropoulos V; Scott LM. 2001. Molecular pathways in bone marrow homing: dominant role of alpha(4)beta(1) over beta(2)-integrins and selectins. Blood 98(8):2403-11. [PubMed: 11588037]  [MGI Ref ID J:115624]

Patrick AL; Rullo J; Beaudin S; Liaw P; Fox-Robichaud AE. 2007. Hepatic leukocyte recruitment in response to time-limited expression of TNF-alpha and IL-1beta. Am J Physiol Gastrointest Liver Physiol 293(4):G663-72. [PubMed: 17656447]  [MGI Ref ID J:126664]

Planck SR; Han YB; Park JM; O'Rourke L; Gutierrez-Ramos JC; Rosenbaum JT. 1998. The effect of genetic deficiency of adhesion molecules on the course of endotoxin-induced uveitis. Curr Eye Res 17(9):941-6. [PubMed: 9746442]  [MGI Ref ID J:114206]

Robinson SD; Frenette PS; Rayburn H; Cummiskey M; Ullman-Cullere M; Wagner DD; Hynes RO. 1999. Multiple, targeted deficiencies in selectins reveal a predominant role for P-selectin in leukocyte recruitment. Proc Natl Acad Sci U S A 96(20):11452-7. [PubMed: 10500197]  [MGI Ref ID J:57973]

Scheiermann C; Kunisaki Y; Lucas D; Chow A; Jang JE; Zhang D; Hashimoto D; Merad M; Frenette PS. 2012. Adrenergic nerves govern circadian leukocyte recruitment to tissues. Immunity 37(2):290-301. [PubMed: 22863835]  [MGI Ref ID J:187383]

Singh I; Zibari GB; Brown MF; Granger DN; Eppihimer M; Zizzi H; Cruz L; Meyer K; Gonzales E; McDonald JC. 1999. Role of P-selectin expression in hepatic ischemia and reperfusion injury. Clin Transplant 13(1 Pt 2):76-82. [PubMed: 10081641]  [MGI Ref ID J:103151]

Sobolev O; Stern P; Lacy-Hulbert A; Hynes RO. 2009. Natural killer cells require selectins for suppression of subcutaneous tumors. Cancer Res 69(6):2531-9. [PubMed: 19258505]  [MGI Ref ID J:146885]

Stokol T; O'Donnell P; Xiao L; Knight S; Stavrakis G; Botto M; von Andrian UH; Mayadas TN. 2004. C1q governs deposition of circulating immune complexes and leukocyte Fcgamma receptors mediate subsequent neutrophil recruitment. J Exp Med 200(7):835-46. [PubMed: 15466618]  [MGI Ref ID J:93949]

Stubke K; Wicklein D; Herich L; Schumacher U; Nehmann N. 2012. Selectin-deficiency reduces the number of spontaneous metastases in a xenograft model of human breast cancer. Cancer Lett 321(1):89-99. [PubMed: 22366582]  [MGI Ref ID J:185633]

Subramaniam M; Frenette PS; Saffaripour S; Johnson RC; Hynes RO; Wagner DD. 1996. Defects in hemostasis in P-selectin-deficient mice. Blood 87(4):1238-42. [PubMed: 8608210]  [MGI Ref ID J:31431]

Subramaniam M; Saffaripour S; Watson SR; Mayadas TN; Hynes RO; Wagner DD. 1995. Reduced recruitment of inflammatory cells in a contact hypersensitivity response in P-selectin-deficient mice. J Exp Med 181(6):2277-82. [PubMed: 7539046]  [MGI Ref ID J:110854]

Sweeney EA; Priestley GV; Nakamoto B; Collins RG; Beaudet AL; Papayannopoulou T. 2000. Mobilization of stem/progenitor cells by sulfated polysaccharides does not require selectin presence. Proc Natl Acad Sci U S A 97(12):6544-9. [PubMed: 10841555]  [MGI Ref ID J:62722]

Tang T; Frenette PS; Hynes RO; Wagner DD; Mayadas TN. 1996. Cytokine-induced meningitis is dramatically attenuated in mice deficient in endothelial selectins. J Clin Invest 97(11):2485-90. [PubMed: 8647940]  [MGI Ref ID J:107411]

Taverna D; Moher H; Crowley D; Borsig L; Varki A; Hynes RO. 2004. Increased primary tumor growth in mice null for beta3- or beta3/beta5-integrins or selectins. Proc Natl Acad Sci U S A 101(3):763-8. [PubMed: 14718670]  [MGI Ref ID J:88109]

Tomita H; Iwata Y; Ogawa F; Komura K; Shimizu K; Yoshizaki A; Hara T; Muroi E; Yanaba K; Bae S; Takenaka M; Hasegawa M; Fujimoto M; Sato S. 2009. P-selectin glycoprotein ligand-1 contributes to wound healing predominantly as a p-selectin ligand and partly as an e-selectin ligand. J Invest Dermatol 129(8):2059-67. [PubMed: 19177138]  [MGI Ref ID J:152512]

Tu L; Poe JC; Kadono T; Venturi GM; Bullard DC; Tedder TF; Steeber DA. 2002. A functional role for circulating mouse L-selectin in regulating leukocyte/endothelial cell interactions in vivo. J Immunol 169(4):2034-43. [PubMed: 12165530]  [MGI Ref ID J:120206]

Wang L; Brown JR; Varki A; Esko JD. 2002. Heparin's anti-inflammatory effects require glucosamine 6-O-sulfation and are mediated by blockade of L- and P-selectins. J Clin Invest 110(1):127-36. [PubMed: 12093896]  [MGI Ref ID J:112426]

Wicklein D; Schmidt A; Labitzky V; Ullrich S; Valent P; Schumacher U. 2013. E- and p-selectins are essential for repopulation of chronic myelogenous and chronic eosinophilic leukemias in a scid mouse xenograft model. PLoS One 8(7):e70139. [PubMed: 23922938]  [MGI Ref ID J:204363]

Yago T; Fu J; McDaniel JM; Miner JJ; McEver RP; Xia L. 2010. Core 1-derived O-glycans are essential E-selectin ligands on neutrophils. Proc Natl Acad Sci U S A 107(20):9204-9. [PubMed: 20439727]  [MGI Ref ID J:160571]

Yamada S; Mayadas TN; Yuan F; Wagner DD; Hynes RO; Melder RJ; Jain RK. 1995. Rolling in P-selectin-deficient mice is reduced but not eliminated in the dorsal skin. Blood 86(9):3487-92. [PubMed: 7579454]  [MGI Ref ID J:29814]

Zaph C; Scott P. 2003. Th1 cell-mediated resistance to cutaneous infection with Leishmania major is independent of P- and E-selectins. J Immunol 171(9):4726-32. [PubMed: 14568948]  [MGI Ref ID J:107364]

Zhang S; Condac E; Qiu H; Jiang J; Gutierrez-Sanchez G; Bergmann C; Handel T; Wang L. 2012. Heparin-induced leukocytosis requires 6-O-sulfation and is caused by blockade of selectin- and CXCL12 protein-mediated leukocyte trafficking in mice. J Biol Chem 287(8):5542-53. [PubMed: 22194593]  [MGI Ref ID J:182444]

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.

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

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Breeding & HusbandryWhen maintained as a live colony, homozygotes may be bred.

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Cryopreserved

Cryopreserved Mice - Ready for Recovery

Price (US dollars $)
Cryorecovery* $2140.00
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 willfulfill 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* $2782.00
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 willfulfill 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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The Jackson Laboratory's Genotype Promise

The Jackson Laboratory has rigorous genetic quality control and mutant gene genotyping programs to ensure the genetic background of JAX® Mice strains as well as the genotypes of strains with identified molecular mutations. JAX® Mice strains are only made available to researchers after meeting our standards. However, the phenotype of each strain may not be fully characterized and/or captured in the strain data sheets. Therefore, we cannot guarantee a strain's phenotype will meet all expectations. To ensure that JAX® Mice will meet the needs of individual research projects or when requesting a strain that is new to your research, we suggest ordering and performing tests on a small number of mice to determine suitability for your particular project.
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"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.

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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.

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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.

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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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