Former Names B6.129S-H2dlAb1-Ea (Changed: 20-SEP-07 ) B6.129-H2dlAb1-Ea/J (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. Mating System Homozygote x Homozygote (Female x Male) 01-MAR-06 Species laboratory mouse Background Strain C57BL/6J Generation N13F2 (18-DEC-12)
Generation DefinitionsDonating Investigator IMR Colony, The Jackson Laboratory Description
Mice that are homozygous null for MHC class II genes H2-Ab1, H2-Aa, H2-Eb1, H2-Eb2, H2-Ea are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities. MHC class II gene products (mRNA or protein) are not detected. A dramatic decrease is observed in the number of CD4 positive T cells in thymus, spleen and lymph nodes. This strain should serve as a suitable recipient of xenogenic Class II MHC transgenes allowing the engineering of mouse models of human MHC Class II-associated diseases.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
A 78.8 kb deletion disrupting Class II MHC genes was induced in 129S2/SvPas-derived H1 embryonic stem (ES) cells via Cre recombination. A hygro-resistance cassette was inserted at the deletion site. The deletion spans from the second exon of the H2-Ab1 gene the third exon of the H2-Ea gene. The H2-Aa, H2-Eb1 and H2-Eb2 genes are completely deleted. Correctly targeted ES cells were injected into C57BL/6 blastocysts. The resulting chimeric animals were bred to C57BL/6 mice. The mice were then backcrossed to C57BL/6J for 12 generations.
| Control | ||
|---|---|---|
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
Strains carrying H2dlAb1-Ea allele
003374 B6;129S2-H2dlAb1-Ea/J View Strains carrying H2dlAb1-Ea (1 strain)
Strains carrying other alleles of H2
006500 129.NOD-(D17Mit175-H2)/J 001649 A.BY H2bc H2-T18f/SnJ-Dstncorn1/J 000140 A.BY-H2bc H2-T18f/SnJ 000472 A.CA-H2f H2-T18a/SnJ 000471 A.SW-H2s H2-T18b/SnJ 001066 A.TH-H2t2/SfDvEgMobJ 001067 A.TL-H2t1/SfDvEgMobJ 002089 AK.B6-H2b Fv1b/J 002090 AK.B6-H2b/J 001094 AK.L-H2b/1CyTyJ 001095 AK.L-H2oz2/CyJ 001096 AK.L-H2oz3/CyJ 000470 AK.M-H2m H2-T18a/nSnJ 003851 ALR.NOD-(D17Mit30-D17Mit123)/Lt 000469 B10.A-H2a H2-T18a/SgSnJ 000468 B10.A-H2h2/(2R)SgSnJ 001150 B10.A-H2h4/(4R)SgDvEgJ 001149 B10.A-H2i3/(3R)SgDvEgJ 000467 B10.A-H2i5 H2-T18a/(5R)SgSnJ 000466 B10.AKM-H2m H2-T18a/SnJ 001954 B10.AQR-H2y1/KljMcdJ 000465 B10.BR-H2k2 H2-T18a/SgSnJ 004804 B10.BR-H2k2 H2-T18a/SgSnJJrep 005308 B10.Cg-H2d Tg(TcraCl4,TcrbCl4)1Shrm/ShrmJ 005534 B10.Cg-H2d Tg(Ins2-HA)165Bri/ShrmJ 010514 B10.Cg-H2g Tg(Cd4-Klra1)6295Dl/J 006446 B10.Cg-H2h4 Sh3pxd2bnee/GrsrJ 006102 B10.Cg-H2k Tg(Il2/NFAT-luc)83Rinc/J 006100 B10.Cg-H2k Tg(NFkB/Fos-luc)26Rinc/J 005895 B10.Cg-Thy1a H2d Tg(TcraCl1,TcrbCl1)1Shrm/J 002024 B10.D1-H2q/SgJ 001163 B10.D2-H2bm23/EgJ 000462 B10.D2-H2d/n2SnJ 001164 B10.D2-H2dm1/EgJ 001151 B10.D2-H2g3/(103R)EgJ 001153 B10.D2-H2i7/(107R)EgJ 001152 B10.D2-H2ia/(106R)EgJ 000460 B10.D2-Hc0 H2d H2-T18c/o2SnJ 000461 B10.D2-Hc0 H2d H2-T18c/oSnJ 000463 B10.D2-Hc1 H2d H2-T18c/nSnJ 003147 B10.D2-Hc1 H2d H2-T18c/nSnJ-Tg(DO11.10)10Dlo/J 000464 B10.DA-H2qp1 H2-T18b/(80NS)SnJ 001823 B10.F-H2bp5/(14R)J 001818 B10.F-H2pb1/(13R)J 001012 B10.HTG-H2g/2CyJ 000999 B10.HTG-H2g/3CyJ 001894 B10.LG-H2ar1/J 000459 B10.M-H2f H2-T18a?/SnJ 002225 B10.M-H2f/nMob Fmn1ld-2J/J 001068 B10.M-H2f/nMobJ 000739 B10.M-H2fm2/MobJ 001154 B10.MBR-H2bq1/SxEgJ 010972 B10.NOD-(rs13459151-rs13483054)/1107MrkJ 001825 B10.P-H2kp1/(10R)SgJ 003199 B10.PL-H2u H2-T18a/(73NS)Sn-Tg(TCRA)B1Jg/J 003200 B10.PL-H2u H2-T18a/(73NS)Sn-Tg(TCRB)C14Jg/J 000458 B10.PL-H2u H2-T18a/(73NS)SnJ 000457 B10.RIII-H2r H2-T18b/(71NS)SnJ 001069 B10.RIII-H2r/(71NS)nMobJ 001760 B10.S-H2as1/(8R)/J 001953 B10.S-H2s/SgMcdJ 001817 B10.S-H2sm1/(12R)SgJ 001650 B10.S-H2t4/(9R)/J 000456 B10.SM H2v H2-T18b/(70NS)Sn-cw/J 001155 B10.T-H2y2/(6R)SgDvEgJ 000445 B10.WB-H2j H2-T18b/SnJ 000444 B10.Y-H2pa H2-T18c/SnJ 003483 B6 x B10.D1-H2q/SgJ-Nox3het-2J/J 003561 B6 x B10.PL-H2u/(73NS)Sn-Hxl/J 002995 B6 x C.B10-H2b/LiMcdJ-Fbn2fp-2J/J 005717 B6(NOD) H2g7-Sostdc1shk/GrsrJ 001148 B6.AK-H2k/FlaEgJ 001895 B6.AK-H2k/J 001160 B6.C-H2bm10/KhEgJ 001161 B6.C-H2bm11/KhEgJ 000364 B6.C-H2bm2/ByJ 000369 B6.C-H2bm4/ByJ 001158 B6.C-H2bm7/KhEgJ 000360 B6.C-H2d Mdmg1BALB/cBy/aByJ 000359 B6.C-H2d/bByJ 001429 B6.C-H2g6/J 005715 B6.Cg H2g7-Tg(Ins2-CD80)3B7Flv/LwnJ 007958 B6.Cg-H2b3/FlaCmwJ 007959 B6.Cg-H2b4/FlaCmwJ 003068 B6.NOD-(Csf2-D11Mit42) (D17Mit21-D17Mit10)/J 004554 B6.NOD-(D17Mit21-D17Mit10) Tg(TCRaAI4)1Dvs/DvsJ 004555 B6.NOD-(D17Mit21-D17Mit10) Tg(TCRbAI4)1Dvs/DvsJ 003300 B6.NOD-(D17Mit21-D17Mit10)/LtJ 003069 B6.NOD-(D1Mit3-Bcl2) (D17Mit21-D17Mit10)/LtJ 003071 B6.NOD-(D1Mit5.1-D1Mit15) (D17Mit21-D17Mit10)/J 003067 B6.NOD-(D3Mit132-Tshb) (D17Mit21-D17Mit10)/J 003066 B6.NOD-(D6Mit54-D6Mit14) (D17Mit21-D17Mit10)/J 000944 B6.SJL-H2b C3c/2CyJ 000966 B6.SJL-H2s C3c/1CyJ 000945 B6.SW/1CyJ 003240 B6;B10.A-H2a-Tg(H2KmPCC)2939Stoe/J 002844 BALB.5R-H2i5/LilJ 001165 BALB/c-H2dm2/KhEgJ 001041 BKS.B6-H2b/J 001892 BRVR.B10-H2b/J 001893 BRVR.D2-H2d/J 002845 C.B-H2b Tg(H2-Dd)D8Gja/LilJ 001952 C.B10-H2b/LilMcdJ 001768 C3.Cg-Irs1Sml H2b/GrsrJ 000443 C3.HTG-H2g H2-T18b?/SnJ 000441 C3.JK-H2j H2-T18b/SnJ 000440 C3.LG-H2ar1/CkcCyJ 000439 C3.NB-H2p H2-T18c?/SnJ 000438 C3.SW-H2b/SnJ 000473 C3H-H2o2 C4bb/SfSnJ 001156 C57BL/6J-H2bm3/EgJ 001157 C57BL/6Kh-H2bm5/KhEgJ 000437 D1.C-H2d H2-T18c/SnJ 000436 D1.DA-H2qp1/SnJ 000435 D1.LP-H2b H2-T18b?/SnJ 000434 LP.RIII-H2r H2-T18b/SnJ 001383 LT.MA-Glo1b H2k/J 002591 NOD.B10Sn-H2b/J 006935 NOD.Cg-H2b thnh/J 004447 NOD.Cg-H2h4/DilTacUmmJ 001626 NOD.NON-H2nb1/LtJ 002032 NOD.SW-H2q/J 001627 NON.NOD-H2g7/LtJ 002974 STOCK Ces1ce H2d/J 001308 STOCK H2473a/J 003154 WLC.C-H2d/MorJ 003153 WLC.Cg-H2d Mtv2a/MorJ View Strains carrying other alleles of H2 (127 strains)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms provided by MGI
assigned by genotype
H2dlAb1-Ea/H2dlAb1-Ea
B6.129S2-H2dlAb1-Ea/J
- mortality/aging
- increased sensitivity to induced morbidity/mortality
- following infection with either a low or high dose of IOE, mice succumb to the infection at 11 to 15 days and 7 to 9 days, respectively, compared to wild-type mice, which succumb at 14 to 17 days and 8 to 12 days, respectively (MGI Ref ID J:123934)
- immune system phenotype
- increased susceptibility to bacterial infection
- mice are more susceptible to infection with a monocytotropic Ehrlichia bacteria from Ixodes ovatrus ticks (IOE) than wild-type mice (MGI Ref ID J:123934)
- following infection with either a low or high dose of IOE, mice succumb to the infection at 11 to 15 days and 7 to 9 days, respectively, compared to wild-type mice, which succumb at 14 to 17 days and 8 to 12 days, respectively (MGI Ref ID J:123934)
- mice have higher burdens of Ehrlichia bacteria in all organs following infection than do wild-type mice (MGI Ref ID J:123934)
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
H2dlAb1-Ea/H2dlAb1-Ea
involves: 129S2/SvPas * C57BL/6
- immune system phenotype
- *normal* immune system phenotype
- stimulated dendritic cells produce normal amounts of IL-12 and TNF-alpha (MGI Ref ID J:157516)
- hematopoietic system phenotype
- abnormal T cell number (MGI Ref ID J:57484)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Immunology, Inflammation and Autoimmunity Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency
MHC class II deficient
Lymphoid Tissue Defects
Internal/Organ Research
Lymphoid Tissue Defects
Research Tools
Immunology and Inflammation Research
MHC class II defects
| Allele Symbol | H2dlAb1-Ea | ||
|---|---|---|---|
| Allele Name | targeted deletion, H2 complex | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | IIdelta; MHC II KO; MHC II-; MHC II0; MHC IIdelta; MHC class IIdelta; MHC-IIdelta; MHCII-; MHCIIdelta; | ||
| Mutation Made By | Christophe Benoist, Joslin Diabetes Center | ||
| Strain of Origin | 129S2/SvPas | ||
| ES Cell Line Name | H1 | ||
| ES Cell Line Strain | 129S2/SvPas | ||
| Gene Symbol and Name | H2, histocompatibility-2, MHC | ||
| Chromosome | 17 | ||
| Gene Common Name(s) | H-2; MHC-II; | ||
| Molecular Note | A 78.8 kb deletion disrupting Class II MHC genes was induced in 129S2/SvPas-derived H1 embryonic stem (ES) cells via Cre recombination. A hygro-resistance cassette was inserted at the deletion site. The deletion spans from the second exon of the H2-Ab1 gene the third exon of the H2-Ea gene. The H2-Aa, H2-Eb1 and H2-Eb2 genes are completely deleted. [MGI Ref ID J:57484] | ||
Genotyping Protocols
H2dlAb1-Ea, Standard PCR
Helpful Links
Genotyping resources and troubleshooting
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H2dlAb1-Ea relatedAiba Y; Kometani K; Hamadate M; Moriyama S; Sakaue-Sawano A; Tomura M; Luche H; Fehling HJ; Casellas R; Kanagawa O; Miyawaki A; Kurosaki T. 2010. Preferential localization of IgG memory B cells adjacent to contracted germinal centers. Proc Natl Acad Sci U S A 107(27):12192-7. [PubMed: 20547847] [MGI Ref ID J:162089]
Alli R; Nguyen P; Boyd K; Sundberg JP; Geiger TL. 2012. A mouse model of clonal CD8+ T lymphocyte-mediated alopecia areata progressing to alopecia universalis. J Immunol 188(1):477-86. [PubMed: 22116824] [MGI Ref ID J:180590]
Aviszus K; Macleod MK; Kirchenbaum GA; Detanico TO; Heiser RA; St Clair JB; Guo W; Wysocki LJ. 2012. Antigen-specific suppression of humoral immunity by anergic Ars/A1 B cells. J Immunol 189(9):4275-83. [PubMed: 23008448] [MGI Ref ID J:190617]
Barrett NA; Rahman OM; Fernandez JM; Parsons MW; Xing W; Austen KF; Kanaoka Y. 2011. Dectin-2 mediates Th2 immunity through the generation of cysteinyl leukotrienes. J Exp Med 208(3):593-604. [PubMed: 21357742] [MGI Ref ID J:176841]
Bienvenu B; Martin B; Auffray C; Cordier C; Becourt C; Lucas B. 2005. Peripheral CD8+CD25+ T lymphocytes from MHC class II-deficient mice exhibit regulatory activity. J Immunol 175(1):246-53. [PubMed: 15972655] [MGI Ref ID J:100582]
Binder CJ; Hartvigsen K; Chang MK; Miller M; Broide D; Palinski W; Curtiss LK; Corr M; Witztum JL. 2004. IL-5 links adaptive and natural immunity specific for epitopes of oxidized LDL and protects from atherosclerosis. J Clin Invest 114(3):427-37. [PubMed: 15286809] [MGI Ref ID J:118092]
Bitsaktsis C; Nandi B; Racine R; MacNamara KC; Winslow G. 2007. T-Cell-independent humoral immunity is sufficient for protection against fatal intracellular ehrlichia infection. Infect Immun 75(10):4933-41. [PubMed: 17664264] [MGI Ref ID J:125283]
Blache C; Adriouch S; Calbo S; Drouot L; Dulauroy S; Arnoult C; Le Corre S; Six A; Seman M; Boyer O. 2009. Cutting edge: CD4-independent development of functional FoxP3+ regulatory t cells. J Immunol 183(7):4182-6. [PubMed: 19767568] [MGI Ref ID J:152754]
Bold TD; Ernst JD. 2012. CD4+ T cell-dependent IFN-gamma production by CD8+ effector T cells in Mycobacterium tuberculosis infection. J Immunol 189(5):2530-6. [PubMed: 22837486] [MGI Ref ID J:189869]
Bosselut R; Feigenbaum L; Sharrow SO; Singer A. 2001. Strength of signaling by CD4 and CD8 coreceptor tails determines the number but not the lineage direction of positively selected thymocytes. Immunity 14(4):483-94. [PubMed: 11336693] [MGI Ref ID J:132432]
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Choi EY; Jung KC; Park HJ; Chung DH; Song JS; Yang SD; Simpson E; Park SH. 2005. Thymocyte-thymocyte interaction for efficient positive selection and maturation of CD4 T cells. Immunity 23(4):387-96. [PubMed: 16226504] [MGI Ref ID J:113276]
Choi YS; Kageyama R; Eto D; Escobar TC; Johnston RJ; Monticelli L; Lao C; Crotty S. 2011. ICOS Receptor Instructs T Follicular Helper Cell versus Effector Cell Differentiation via Induction of the Transcriptional Repressor Bcl6. Immunity 34(6):932-46. [PubMed: 21636296] [MGI Ref ID J:174012]
Conlon TM; Cole JL; Motallebzadeh R; Harper I; Callaghan CJ; Bolton EM; Bradley JA; Saeb-Parsy K; Pettigrew GJ. 2012. Unlinked memory helper responses promote long-lasting humoral alloimmunity. J Immunol 189(12):5703-12. [PubMed: 23162131] [MGI Ref ID J:190849]
Conlon TM; Saeb-Parsy K; Cole JL; Motallebzadeh R; Qureshi MS; Rehakova S; Negus MC; Callaghan CJ; Bolton EM; Bradley JA; Pettigrew GJ. 2012. Germinal center alloantibody responses are mediated exclusively by indirect-pathway CD4 T follicular helper cells. J Immunol 188(6):2643-52. [PubMed: 22323543] [MGI Ref ID J:181855]
Deenick EK; Chan A; Ma CS; Gatto D; Schwartzberg PL; Brink R; Tangye SG. 2010. Follicular helper T cell differentiation requires continuous antigen presentation that is independent of unique B cell signaling. Immunity 33(2):241-53. [PubMed: 20691615] [MGI Ref ID J:163920]
Do JS; Valujskikh A; Vignali DA; Fairchild RL; Min B. 2012. Unexpected role for MHC II-peptide complexes in shaping CD8 T-cell expansion and differentiation in vivo. Proc Natl Acad Sci U S A 109(31):12698-703. [PubMed: 22802622] [MGI Ref ID J:188517]
Do JS; Visperas A; Oh K; Stohlman SA; Min B. 2012. Memory CD4 T cells induce selective expression of IL-27 in CD8+ dendritic cells and regulate homeostatic naive T cell proliferation. J Immunol 188(1):230-7. [PubMed: 22116827] [MGI Ref ID J:180589]
Feuillet V; Lucas B; Di Santo JP; Bismuth G; Trautmann A. 2005. Multiple survival signals are delivered by dendritic cells to naive CD4+ T cells. Eur J Immunol 35(9):2563-72. [PubMed: 16078277] [MGI Ref ID J:113487]
Freeman ML; Burkum CE; Woodland DL; Sun R; Wu TT; Blackman MA. 2012. Importance of antibody in virus infection and vaccine-mediated protection by a latency-deficient recombinant murine gamma-herpesvirus-68. J Immunol 188(3):1049-56. [PubMed: 22198955] [MGI Ref ID J:180759]
Friese MA; Jakobsen KB; Friis L; Etzensperger R; Craner MJ; McMahon RM; Jensen LT; Huygelen V; Jones EY; Bell JI; Fugger L. 2008. Opposing effects of HLA class I molecules in tuning autoreactive CD8+ T cells in multiple sclerosis. Nat Med 14(11):1227-35. [PubMed: 18953350] [MGI Ref ID J:144083]
Getahun A; Smith MJ; Kogut I; van Dyk LF; Cambier JC. 2012. Retention of anergy and inhibition of antibody responses during acute gamma herpesvirus 68 infection. J Immunol 189(6):2965-74. [PubMed: 22904300] [MGI Ref ID J:189918]
Grover HS; Blanchard N; Gonzalez F; Chan S; Robey EA; Shastri N. 2012. The Toxoplasma gondii Peptide AS15 Elicits CD4 T Cells That Can Control Parasite Burden. Infect Immun 80(9):3279-88. [PubMed: 22778097] [MGI Ref ID J:187170]
Guimond M; Veenstra RG; Grindler DJ; Zhang H; Cui Y; Murphy RD; Kim SY; Na R; Hennighausen L; Kurtulus S; Erman B; Matzinger P; Merchant MS; Mackall CL. 2009. Interleukin 7 signaling in dendritic cells regulates the homeostatic proliferation and niche size of CD4+ T cells. Nat Immunol 10(2):149-57. [PubMed: 19136960] [MGI Ref ID J:144504]
Henri S; Poulin LF; Tamoutounour S; Ardouin L; Guilliams M; de Bovis B; Devilard E; Viret C; Azukizawa H; Kissenpfennig A; Malissen B. 2010. CD207+ CD103+ dermal dendritic cells cross-present keratinocyte-derived antigens irrespective of the presence of Langerhans cells. J Exp Med 207(1):189-206, S1-6. [PubMed: 20038600] [MGI Ref ID J:156820]
Houston EG Jr; Fink PJ. 2009. MHC drives TCR repertoire shaping, but not maturation, in recent thymic emigrants. J Immunol 183(11):7244-9. [PubMed: 19915060] [MGI Ref ID J:157387]
Iijima N; Mattei LM; Iwasaki A. 2011. Recruited inflammatory monocytes stimulate antiviral Th1 immunity in infected tissue. Proc Natl Acad Sci U S A 108(1):284-9. [PubMed: 21173243] [MGI Ref ID J:169008]
Ismail N; Crossley EC; Stevenson HL; Walker DH. 2007. Relative importance of T-cell subsets in monocytotropic ehrlichiosis: a novel effector mechanism involved in ehrlichia-induced immunopathology in murine ehrlichiosis. Infect Immun 75(9):4608-20. [PubMed: 17562770] [MGI Ref ID J:123934]
Jacobsen EA; Zellner KR; Colbert D; Lee NA; Lee JJ. 2011. Eosinophils regulate dendritic cells and Th2 pulmonary immune responses following allergen provocation. J Immunol 187(11):6059-68. [PubMed: 22048766] [MGI Ref ID J:179701]
Kang TW; Yevsa T; Woller N; Hoenicke L; Wuestefeld T; Dauch D; Hohmeyer A; Gereke M; Rudalska R; Potapova A; Iken M; Vucur M; Weiss S; Heikenwalder M; Khan S; Gil J; Bruder D; Manns M; Schirmacher P; Tacke F; Ott M; Luedde T; Longerich T; Kubicka S; Zender L. 2011. Senescence surveillance of pre-malignant hepatocytes limits liver cancer development. Nature 479(7374):547-51. [PubMed: 22080947] [MGI Ref ID J:179823]
Kastenmuller W; Gasteiger G; Subramanian N; Sparwasser T; Busch DH; Belkaid Y; Drexler I; Germain RN. 2011. Regulatory T cells selectively control CD8+ T cell effector pool size via IL-2 restriction. J Immunol 187(6):3186-97. [PubMed: 21849683] [MGI Ref ID J:179230]
Krebs P; Barnes MJ; Lampe K; Whitley K; Bahjat KS; Beutler B; Janssen E; Hoebe K. 2009. NK cell-mediated killing of target cells triggers robust antigen-specific T cell-mediated and humoral responses. Blood 113(26):6593-602. [PubMed: 19406986] [MGI Ref ID J:150150]
Kupfer TM; Crawford ML; Pham K; Gill RG. 2005. MHC-mismatched islet allografts are vulnerable to autoimmune recognition in vivo. J Immunol 175(4):2309-16. [PubMed: 16081800] [MGI Ref ID J:107508]
Larena M; Regner M; Lee E; Lobigs M. 2011. Pivotal role of antibody and subsidiary contribution of CD8+ T cells to recovery from infection in a murine model of Japanese encephalitis. J Virol :. [PubMed: 21450826] [MGI Ref ID J:171204]
Le Campion A; Gagnerault MC; Auffray C; Becourt C; Poitrasson-Riviere M; Lallemand E; Bienvenu B; Martin B; Lepault F; Lucas B. 2009. Lymphopenia-induced spontaneous T-cell proliferation as a cofactor for autoimmune disease development. Blood 114(9):1784-93. [PubMed: 19561321] [MGI Ref ID J:152255]
Le Campion A; Pommier A; Delpoux A; Stouvenel L; Auffray C; Martin B; Lucas B. 2012. IL-2 and IL-7 determine the homeostatic balance between the regulatory and conventional CD4+ T cell compartments during peripheral T cell reconstitution. J Immunol 189(7):3339-46. [PubMed: 22933631] [MGI Ref ID J:190347]
Lee YJ; Jeon YK; Kang BH; Chung DH; Park CG; Shin HY; Jung KC; Park SH. 2010. Generation of PLZF+ CD4+ T cells via MHC class II-dependent thymocyte-thymocyte interaction is a physiological process in humans. J Exp Med 207(1):237-46, S1-7. [PubMed: 20038602] [MGI Ref ID J:156545]
Lemessurier K; Hacker H; Tuomanen E; Redecke V. 2010. Inhibition of T Cells Provides Protection against Early Invasive Pneumococcal Disease. Infect Immun 78(12):5287-94. [PubMed: 20855509] [MGI Ref ID J:165973]
Liu X; Zhan Z; Li D; Xu L; Ma F; Zhang P; Yao H; Cao X. 2011. Intracellular MHC class II molecules promote TLR-triggered innate immune responses by maintaining activation of the kinase Btk. Nat Immunol 12(5):416-24. [PubMed: 21441935] [MGI Ref ID J:171920]
Logunova NN; Viret C; Pobezinsky LA; Miller SA; Kazansky DB; Sundberg JP; Chervonsky AV. 2005. Restricted MHC-peptide repertoire predisposes to autoimmunity. J Exp Med 202(1):73-84. [PubMed: 15998789] [MGI Ref ID J:100625]
London A; Itskovich E; Benhar I; Kalchenko V; Mack M; Jung S; Schwartz M. 2011. Neuroprotection and progenitor cell renewal in the injured adult murine retina requires healing monocyte-derived macrophages. J Exp Med 208(1):23-39. [PubMed: 21220455] [MGI Ref ID J:176855]
Maehr R; Hang HC; Mintern JD; Kim YM; Cuvillier A; Nishimura M; Yamada K; Shirahama-Noda K; Hara-Nishimura I; Ploegh HL. 2005. Asparagine endopeptidase is not essential for class II MHC antigen presentation but is required for processing of cathepsin L in mice. J Immunol 174(11):7066-74. [PubMed: 15905550] [MGI Ref ID J:99005]
Maehr R; Kraus M; Ploegh HL. 2004. Mice deficient in invariant-chain and MHC class II exhibit a normal mature B2 cell compartment. Eur J Immunol 34(8):2230-6. [PubMed: 15259020] [MGI Ref ID J:91771]
Majewski M; Bose TO; Sille FC; Pollington AM; Fiebiger E; Boes M. 2007. Protein kinase C delta stimulates antigen presentation by Class II MHC in murine dendritic cells. Int Immunol 19(6):719-32. [PubMed: 17446207] [MGI Ref ID J:122307]
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Nakamura T; Sonoda KH; Faunce DE; Gumperz J; Yamamura T; Miyake S; Stein-Streilein J. 2003. CD4+ NKT cells, but not conventional CD4+ T cells, are required to generate efferent CD8+ T regulatory cells following antigen inoculation in an immune-privileged site. J Immunol 171(3):1266-71. [PubMed: 12874214] [MGI Ref ID J:120214]
Northrop JK; Thomas RM; Wells AD; Shen H. 2006. Epigenetic remodeling of the IL-2 and IFN-gamma loci in memory CD8 T cells is influenced by CD4 T cells. J Immunol 177(2):1062-9. [PubMed: 16818762] [MGI Ref ID J:134945]
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Animal Health Reports
Room Number AX12
Colony Maintenance
Breeding & Husbandry This strain originated on a mixed B6,129S background and is maintained on a congenic B6.129 background. Reproduction is fair. The strain is immunodeficient and sensitive to poor microbiological conditions. Pneumocystis can be a problem. Expected coat color expected from breeding:Black. Mating System Homozygote x Homozygote (Female x Male) 01-MAR-06 Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
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Price per mouse (US dollars $) Gender Genotypes Provided Individual Mouse $145.00 Female or Male Homozygous for H2dlAb1-Ea
Price per Pair (US dollars $) Pair Genotype $290.00 Homozygous for H2dlAb1-Ea x Homozygous for H2dlAb1-Ea Standard Supply
Repository-Live. Repository-Live represents an exclusive set of over 1500 unique mouse models maintained at The Jackson Laboratory to support a vast array of research areas. The breeding colonies for Repository Strains provide mice for both large and small orders and fluctuate in size depending on current demand for each strain. Repository-live orders are treated as custom orders. Within 2 business days, we respond to each availability inquiry or order with various delivery options. Repository Strains typically are delivered at 4 to 8 weeks of age and will not exceed 12 weeks of age on the day of shipping.
| Pricing for International shipping destinations |
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Price per mouse (US dollars $) Gender Genotypes Provided Individual Mouse $188.50 Female or Male Homozygous for H2dlAb1-Ea
Price per Pair (US dollars $) Pair Genotype $377.00 Homozygous for H2dlAb1-Ea x Homozygous for H2dlAb1-Ea Standard Supply
Repository-Live. Repository-Live represents an exclusive set of over 1500 unique mouse models maintained at The Jackson Laboratory to support a vast array of research areas. The breeding colonies for Repository Strains provide mice for both large and small orders and fluctuate in size depending on current demand for each strain. Repository-live orders are treated as custom orders. Within 2 business days, we respond to each availability inquiry or order with various delivery options. Repository Strains typically are delivered at 4 to 8 weeks of age and will not exceed 12 weeks of age on the day of shipping.
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Repository-Live. Repository-Live represents an exclusive set of over 1500 unique mouse models maintained at The Jackson Laboratory to support a vast array of research areas. The breeding colonies for Repository Strains provide mice for both large and small orders and fluctuate in size depending on current demand for each strain. Repository-live orders are treated as custom orders. Within 2 business days, we respond to each availability inquiry or order with various delivery options. Repository Strains typically are delivered at 4 to 8 weeks of age and will not exceed 12 weeks of age on the day of shipping.
| Control | ||
|---|---|---|
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
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