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Former Names NOD.129P2(B6)-Selltm1Tft/1Lt (Changed: 17-FEB-06 ) NOD-Sell- (Changed: 15-DEC-04 ) Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Species laboratory mouse Background Strain NOD/ShiLt Donor Strain 129P2/OlaHsd H2 Haplotype g7 Generation N10F22p
Generation DefinitionsDonating Investigator Dr. Edward Leiter, The Jackson Laboratory Appearance
albino, pink eyed
Related Genotype: A/A Tyrc/Tyrc
| Control | ||
|---|---|---|
| 001976 NOD/ShiLtJ | ||
| Considerations for Choosing Controls | ||
Strains carrying Selltm1Tft allele
004943 NOD.Cg-Selltm1Tft Itgb7tm1Cgn/LtJ View Strains carrying Selltm1Tft (1 strain)
Strains carrying other alleles of Sell
View Strains carrying other alleles of Sell (9 strains)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Selltm1Tft relatedInternal/Organ Research
Wound Healing
delayed/impaired
Immunology, Inflammation and Autoimmunity Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
| Allele Symbol | Selltm1Tft | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Thomas F Tedder | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | CD62L KO; CD62L-; L-selectin-; L-; selectin-; | ||
| Mutation Made By | Dr. Thomas Tedder, Duke University Medical Center | ||
| Strain of Origin | 129P2/OlaHsd | ||
| ES Cell Line Name | E14.1 | ||
| ES Cell Line Strain | 129P2/OlaHsd | ||
| Gene Symbol and Name | Sell, selectin, lymphocyte | ||
| Chromosome | 1 | ||
| Gene Common Name(s) | A.11; AI528707; CD62L; L-selectin; LAM1; LECAM-1; LECAM1; LEU8; LNHR; LSEL; LYAM1; Lnhr; Ly-22; Ly-m22; Lyam-1; Lyam1; PLNHR; TQ1; expressed sequence AI528707; lymph node homing receptor; lymphocyte adhesion molecule 1; lymphocyte antigen 22; lymphocyte antigen m22; | ||
| Molecular Note | A neomycin resistance gene replaced the majority of the exon encoding the L-selectin domain. [MGI Ref ID J:25005] | ||
Mora C; Grewal IS; Wong FS; Flavell RA. 2004. Role of L-selectin in the development of autoimmune diabetes in non-obese diabetic mice. Int Immunol 16(2):257-64. [PubMed: 14734611] [MGI Ref ID J:88974]
Nagaoka T; Kaburagi Y; Hamaguchi Y; Hasegawa M; Takehara K; Steeber DA; Tedder TF; Sato S. 2000. Delayed wound healing in the absence of intercellular adhesion molecule-1 or L-selectin expression. Am J Pathol 157(1):237-47. [PubMed: 10880393] [MGI Ref ID J:63135]
Selltm1Tft relatedAnderson BE; Taylor PA; McNiff JM; Jain D; Demetris AJ; Panoskaltsis-Mortari A; Ager A; Blazar BR; Shlomchik WD; Shlomchik MJ. 2008. Effects of donor T-cell trafficking and priming site on graft-versus-host disease induction by naive and memory phenotype CD4 T cells. Blood 111(10):5242-51. [PubMed: 18285547] [MGI Ref ID J:135662]
Arbones ML; Ord DC; Ley K; Ratech H; Maynard-Curry C; Otten G; Capon DJ; Tedder TF. 1994. Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice. Immunity 1(4):247-60. [PubMed: 7534203] [MGI Ref ID J:25005]
Bae SJ; Shimizu K; Yozaki M; Yamaoka T; Akiyama Y; Yoshizaki A; Muroi E; Hara T; Ogawa F; Sato S. 2010. Involvement of L-selectin in contact hypersensitivity responses augmented by auditory stress. Am J Pathol 176(1):187-97. [PubMed: 19948832] [MGI Ref ID J:156378]
Diacovo TG; Blasius AL; Mak TW; Cella M; Colonna M. 2005. Adhesive mechanisms governing interferon-producing cell recruitment into lymph nodes. J Exp Med 202(5):687-96. [PubMed: 16147979] [MGI Ref ID J:100718]
Doyle NA; Bhagwan SD; Meek BB; Kutkoski GJ; Steeber DA; Tedder TF; Doerschuk CM. 1997. Neutrophil margination, sequestration, and emigration in the lungs of L-selectin-deficient mice. J Clin Invest 99(3):526-33. [PubMed: 9022088] [MGI Ref ID J:39042]
Forbes E; Hulett M; Ahrens R; Wagner N; Smart V; Matthaei KI; Brandt EB; Dent LA; Rothenberg ME; Tang M; Foster PS; Hogan SP. 2006. ICAM-1-dependent pathways regulate colonic eosinophilic inflammation. J Leukoc Biol 80(2):330-41. [PubMed: 16731772] [MGI Ref ID J:111227]
Forlow SB; Ley K. 2001. Selectin-independent leukocyte rolling and adhesion in mice deficient in E-, P-, and L-selectin and ICAM-1. Am J Physiol Heart Circ Physiol 280(2):H634-41. [PubMed: 11158961] [MGI Ref ID J:68044]
Friedline RH; Wong CP; Steeber DA; Tedder TF; Tisch R. 2002. L-selectin is not required for T cell-mediated autoimmune diabetes. J Immunol 168(6):2659-66. [PubMed: 11884430] [MGI Ref ID J:126855]
Galkina E; Florey O; Zarbock A; Smith BR; Preece G; Lawrence MB; Haskard DO; Ager A. 2007. T lymphocyte rolling and recruitment into peripheral lymph nodes is regulated by a saturable density of L-selectin (CD62L). Eur J Immunol 37(5):1243-53. [PubMed: 17429841] [MGI Ref ID J:123557]
Galkina E; Kadl A; Sanders J; Varughese D; Sarembock IJ; Ley K. 2006. Lymphocyte recruitment into the aortic wall before and during development of atherosclerosis is partially L-selectin dependent. J Exp Med 203(5):1273-82. [PubMed: 16682495] [MGI Ref ID J:124135]
Galkina E; Tanousis K; Preece G; Tolaini M; Kioussis D; Florey O; Haskard DO; Tedder TF; Ager A. 2003. L-selectin shedding does not regulate constitutive T cell trafficking but controls the migration pathways of antigen-activated T lymphocytes. J Exp Med 198(9):1323-35. [PubMed: 14597735] [MGI Ref ID J:86473]
Hafezi-Moghadam A; Thomas KL; Prorock AJ; Huo Y; Ley K. 2001. L-selectin shedding regulates leukocyte recruitment. J Exp Med 193(7):863-72. [PubMed: 11283159] [MGI Ref ID J:120579]
Hamaguchi Y; Nishizawa Y; Yasui M; Hasegawa M; Kaburagi Y; Komura K; Nagaoka T; Saito E; Shimada Y; Takehara K; Kadono T; Steeber DA; Tedder TF; Sato S. 2002. Intercellular adhesion molecule-1 and L-selectin regulate bleomycin-induced lung fibrosis. Am J Pathol 161(5):1607-18. [PubMed: 12414509] [MGI Ref ID J:79905]
Hickey MJ; Forster M; Mitchell D; Kaur J; De Caigny C; Kubes P. 2000. L-Selectin facilitates emigration and extravascular locomotion of leukocytes during acute inflammatory responses In vivo J Immunol 165(12):7164-70. [PubMed: 11120848] [MGI Ref ID J:66107]
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]
Jung U; Ley K. 1999. Mice lacking two or all three selectins demonstrate overlapping and distinct functions for each selectin. J Immunol 162(11):6755-62. [PubMed: 10352295] [MGI Ref ID J:55032]
Jung U; Ramos CL; Bullard DC; Ley K. 1998. Gene-targeted mice reveal importance of L-selectin-dependent rolling for neutrophil adhesion. Am J Physiol 274(5 Pt 2):H1785-91. [PubMed: 9612391] [MGI Ref ID J:47723]
Kaburagi Y; Hasegawa M; Nagaoka T; Shimada Y; Hamaguchi Y; Komura K; Saito E; Yanaba K; Takehara K; Kadono T; Steeber DA; Tedder TF; Sato S. 2002. The cutaneous reverse Arthus reaction requires intercellular adhesion molecule 1 and L-selectin expression. J Immunol 168(6):2970-8. [PubMed: 11884469] [MGI Ref ID J:112251]
Kanwar S; Steeber DA; Tedder TF; Hickey MJ; Kubes P. 1999. Overlapping roles for L-selectin and P-selectin in antigen-induced immune responses in the microvasculature. J Immunol 162(5):2709-16. [PubMed: 10072515] [MGI Ref ID J:111002]
Kawasuji A; Hasegawa M; Horikawa M; Fujita T; Matsushita Y; Matsushita T; Fujimoto M; Steeber DA; Tedder TF; Takehara K; Sato S. 2006. L-selectin and intercellular adhesion molecule-1 regulate the development of Concanavalin A-induced liver injury. J Leukoc Biol 79(4):696-705. [PubMed: 16461740] [MGI Ref ID J:107551]
Komura K; Hasegawa M; Hamaguchi Y; Saito E; Kaburagi Y; Yanaba K; Kawara S; Takehara K; Seki M; Steeber DA; Tedder TF; Sato S. 2003. Ultraviolet light exposure suppresses contact hypersensitivity by abrogating endothelial intercellular adhesion molecule-1 up-regulation at the elicitation site. J Immunol 171(6):2855-62. [PubMed: 12960307] [MGI Ref ID J:85377]
Komura K; Iwata Y; Ogawa F; Yoshizaki A; Yamaoka T; Akiyama Y; Hara T; Hasegawa M; Fujimoto M; Sato S. 2009. Low zone tolerance requires ICAM-1 expression to limit contact hypersensitivity elicitation. J Invest Dermatol 129(11):2661-7. [PubMed: 19536145] [MGI Ref ID J:157133]
Kunkel EJ; Chomas JE; Ley K. 1998. Role of primary and secondary capture for leukocyte accumulation in vivo. Circ Res 82(1):30-8. [PubMed: 9440702] [MGI Ref ID J:114235]
Kunkel EJ; Ramos CL; Steeber DA; Muller W; Wagner N; Tedder TF; Ley K. 1998. The roles of L-selectin, beta 7 integrins, and P-selectin in leukocyte rolling and adhesion in high endothelial venules of Peyer's patches. J Immunol 161(5):2449-56. [PubMed: 9725243] [MGI Ref ID J:112049]
Matsushita Y; Hasegawa M; Matsushita T; Fujimoto M; Horikawa M; Fujita T; Kawasuji A; Ogawa F; Steeber DA; Tedder TF; Takehara K; Sato S. 2007. Intercellular adhesion molecule-1 deficiency attenuates the development of skin fibrosis in tight-skin mice. J Immunol 179(1):698-707. [PubMed: 17579093] [MGI Ref ID J:143152]
Nagaoka T; Kaburagi Y; Hamaguchi Y; Hasegawa M; Takehara K; Steeber DA; Tedder TF; Sato S. 2000. Delayed wound healing in the absence of intercellular adhesion molecule-1 or L-selectin expression. Am J Pathol 157(1):237-47. [PubMed: 10880393] [MGI Ref ID J:63135]
Nakano H; Yanagita M; Gunn MD. 2001. CD11c(+)B220(+)Gr-1(+) cells in mouse lymph nodes and spleen display characteristics of plasmacytoid dendritic cells. J Exp Med 194(8):1171-8. [PubMed: 11602645] [MGI Ref ID J:118783]
Ogawa A; Yoshizaki A; Yanaba K; Ogawa F; Hara T; Muroi E; Takenaka M; Shimizu K; Hasegawa M; Fujimoto M; Tedder TF; Sato S. 2010. The differential role of L-selectin and ICAM-1 in Th1-type and Th2-type contact hypersensitivity. J Invest Dermatol 130(6):1558-70. [PubMed: 20182448] [MGI Ref ID J:160092]
Ostanin DV; Furr KL; Pavlick KP; Gray L; Kevil CG; Shukla D; D'Souza D; Hoffman JM; Grisham MB. 2007. T cell-associated CD18 but not CD62L, ICAM-1, or PSGL-1 is required for the induction of chronic colitis. Am J Physiol Gastrointest Liver Physiol 292(6):G1706-14. [PubMed: 17332469] [MGI Ref ID J:123696]
Ridger VC; Hellewell PG; Norman KE. 2005. L- and P-selectins collaborate to support leukocyte rolling in vivo when high-affinity P-selectin-P-selectin glycoprotein ligand-1 interaction is inhibited. Am J Pathol 166(3):945-52. [PubMed: 15743805] [MGI Ref ID J:96776]
Rosenzweig HL; Martin TM; Jann MM; Planck SR; Davey MP; Kobayashi K; Flavell RA; Rosenbaum JT. 2008. NOD2, the gene responsible for familial granulomatous uveitis, in a mouse model of uveitis. Invest Ophthalmol Vis Sci 49(4):1518-24. [PubMed: 18385071] [MGI Ref ID J:136140]
Schuster K; Gadiot J; Andreesen R; Mackensen A; Gajewski TF; Blank C. 2009. Homeostatic proliferation of naive CD8(+) T cells depends on CD62L/L-selectin-mediated homing to peripheral LN. Eur J Immunol 39(11):2981-2990. [PubMed: 19658092] [MGI Ref ID J:154207]
Shigeta A; Matsumoto M; Tedder TF; Lowe JB; Miyasaka M; Hirata T. 2008. An L-selectin ligand distinct from P-selectin glycoprotein ligand-1 is expressed on endothelial cells and promotes neutrophil rolling in inflammation. Blood 112(13):4915-23. [PubMed: 18818390] [MGI Ref ID J:144251]
Shimada Y; Hasegawa M; Kaburagi Y; Hamaguchi Y; Komura K; Saito E; Takehara K; Steeber DA; Tedder TF; Sato S. 2003. L-selectin or ICAM-1 deficiency reduces an immediate-type hypersensitivity response by preventing mast cell recruitment in repeated elicitation of contact hypersensitivity. J Immunol 170(8):4325-34. [PubMed: 12682269] [MGI Ref ID J:125436]
Sinclair LV; Finlay D; Feijoo C; Cornish GH; Gray A; Ager A; Okkenhaug K; Hagenbeek TJ; Spits H; Cantrell DA. 2008. Phosphatidylinositol-3-OH kinase and nutrient-sensing mTOR pathways control T lymphocyte trafficking. Nat Immunol 9(5):513-21. [PubMed: 18391955] [MGI Ref ID J:134510]
Smith ML; Olson TS; Ley K. 2004. CXCR2- and E-selectin-induced neutrophil arrest during inflammation in vivo. J Exp Med 200(7):935-9. [PubMed: 15466624] [MGI Ref ID J:93946]
Steeber DA; Campbell MA; Basit A; Ley K; Tedder TF. 1998. Optimal selectin-mediated rolling of leukocytes during inflammation in vivo requires intercellular adhesion molecule-1 expression. Proc Natl Acad Sci U S A 95(13):7562-7. [PubMed: 9636189] [MGI Ref ID J:48271]
Steeber DA; Green NE; Sato S; Tedder TF. 1996. Humoral immune responses in L-selectin-deficient mice. J Immunol 157(11):4899-907. [PubMed: 8943394] [MGI Ref ID J:37490]
Steeber DA; Tang ML; Green NE; Zhang XQ; Sloane JE; Tedder TF. 1999. Leukocyte entry into sites of inflammation requires overlapping interactions between the L-selectin and ICAM-1 pathways. J Immunol 163(4):2176-86. [PubMed: 10438959] [MGI Ref ID J:57424]
Steeber DA; Tang ML; Zhang XQ; Muller W; Wagner N; Tedder TF. 1998. Efficient lymphocyte migration across high endothelial venules of mouse Peyer's patches requires overlapping expression of L-selectin and beta7 integrin. J Immunol 161(12):6638-47. [PubMed: 9862692] [MGI Ref ID J:112112]
Subramanian H; Grailer JJ; Ohlrich KC; Rymaszewski AL; Loppnow JJ; Kodera M; Conway RM; Steeber DA. 2012. Signaling through L-selectin mediates enhanced chemotaxis of lymphocyte subsets to secondary lymphoid tissue chemokine. J Immunol 188(7):3223-36. [PubMed: 22387549] [MGI Ref ID J:183093]
Tang ML; Hale LP; Steeber DA; Tedder TF. 1997. L-selectin is involved in lymphocyte migration to sites of inflammation in the skin: delayed rejection of allografts in L-selectin-deficient mice. J Immunol 158(11):5191-9. [PubMed: 9164936] [MGI Ref ID J:40629]
Tang ML; Steeber DA; Zhang XQ; Tedder TF. 1998. Intrinsic differences in L-selectin expression levels affect T and B lymphocyte subset-specific recirculation pathways. J Immunol 160(10):5113-21. [PubMed: 9590263] [MGI Ref ID J:47480]
Tedder TF; Steeber DA; Pizcueta P. 1995. L-selectin-deficient mice have impaired leukocyte recruitment into inflammatory sites. J Exp Med 181(6):2259-64. [PubMed: 7539045] [MGI Ref ID J:26621]
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]
Venturi GM; Conway RM; Steeber DA; Tedder TF. 2007. CD25+CD4+ regulatory T cell migration requires L-selectin expression: L-selectin transcriptional regulation balances constitutive receptor turnover. J Immunol 178(1):291-300. [PubMed: 17182566] [MGI Ref ID J:141931]
Venturi GM; Tu L; Kadono T; Khan AI; Fujimoto Y; Oshel P; Bock CB; Miller AS; Albrecht RM; Kubes P; Steeber DA; Tedder TF. 2003. Leukocyte migration is regulated by L-selectin endoproteolytic release. Immunity 19(5):713-24. [PubMed: 14614858] [MGI Ref ID J:142184]
Wagner N; Lohler J; Tedder TF; Rajewsky K; Muller W; Steeber DA. 1998. L-selectin and beta7 integrin synergistically mediate lymphocyte migration to mesenteric lymph nodes. Eur J Immunol 28(11):3832-9. [PubMed: 9842926] [MGI Ref ID J:114211]
Wang L; Fuster M; Sriramarao P; Esko JD. 2005. Endothelial heparan sulfate deficiency impairs L-selectin- and chemokine-mediated neutrophil trafficking during inflammatory responses. Nat Immunol 6(9):902-10. [PubMed: 16056228] [MGI Ref ID J:100456]
Yamada M; Yanaba K; Hasegawa M; Matsushita Y; Horikawa M; Komura K; Matsushita T; Kawasuji A; Fujita T; Takehara K; Steeber DA; Tedder TF; Sato S. 2006. Regulation of local and metastatic host-mediated anti-tumour mechanisms by L-selectin and intercellular adhesion molecule-1. Clin Exp Immunol 143(2):216-27. [PubMed: 16412045] [MGI Ref ID J:108135]
Yoshizaki A; Yanaba K; Iwata Y; Komura K; Ogawa A; Akiyama Y; Muroi E; Hara T; Ogawa F; Takenaka M; Shimizu K; Hasegawa M; Fujimoto M; Tedder TF; Sato S. 2010. Cell Adhesion Molecules Regulate Fibrotic Process via Th1/Th2/Th17 Cell Balance in a Bleomycin-Induced Scleroderma Model. J Immunol 185(4):2502-15. [PubMed: 20624949] [MGI Ref ID J:162381]
Yukami T; Hasegawa M; Matsushita Y; Fujita T; Matsushita T; Horikawa M; Komura K; Yanaba K; Hamaguchi Y; Nagaoka T; Ogawa F; Fujimoto M; Steeber DA; Tedder TF; Takehara K; Sato S. 2007. Endothelial selectins regulate skin wound healing in cooperation with L-selectin and ICAM-1. J Leukoc Biol 82(3):519-31. [PubMed: 17595378] [MGI Ref ID J:124291]
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]
Animal Health Reports
Production of mice from cryopreserved embryos or sperm occurs in a maximum barrier room, G200.
| Pricing for USA, Canada and Mexico shipping destinations |
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Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $2250.00 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.
Embryos
Price (US dollars $) Frozen Embryo $1600.00 Standard Supply
Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.
Supply Notes
- Cryopreserved Embryos
Available to most shipping destinations1
This strain is also available as cryopreserved embryos2. Orders for cryopreserved embryos may be placed with our Customer Service Department. Experienced technicians at The Jackson Laboratory have recovered frozen embryos of this strain successfully. We will provide you enough embryos to perform two embryo transfers. The Jackson Laboratory does not guarantee successful recovery at your facility. For complete information on purchasing embryos, please visit our Cryopreserved Embryos web page.
1 Shipments cannot be made to Australia due to Australian government import restrictions.
2 Embryos for most strains are cryopreserved at the two cell stage while some strains are cryopreserved at the eight cell stage. If this information is important to you, please contact Customer Service.- 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 11 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 |
|
Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $2925.00 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.
Embryos
Price (US dollars $) Frozen Embryo $2080.00 Standard Supply
Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.
Supply Notes
- Cryopreserved Embryos
Available to most shipping destinations1
This strain is also available as cryopreserved embryos2. Orders for cryopreserved embryos may be placed with our Customer Service Department. Experienced technicians at The Jackson Laboratory have recovered frozen embryos of this strain successfully. We will provide you enough embryos to perform two embryo transfers. The Jackson Laboratory does not guarantee successful recovery at your facility. For complete information on purchasing embryos, please visit our Cryopreserved Embryos web page.
1 Shipments cannot be made to Australia due to Australian government import restrictions.
2 Embryos for most strains are cryopreserved at the two cell stage while some strains are cryopreserved at the eight cell stage. If this information is important to you, please contact Customer Service.- 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 11 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).
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Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.
| Control | ||
|---|---|---|
| 001976 NOD/ShiLtJ | ||
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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