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New
JAX® Microinjection Services
We
offer both DNA microinjection and ES cell microinjection
services to producing genetically
modified mice.
Research tools for neurobiological research
Looking
for Cre-, fluorescent protein-, FLP-FRT-, TET -,
or lacZ-expressing mouse strains for
your neurobiology research? Check out the Research
Tools section of the JAX® Mice
Database. Learn more about this new resource
at our website.
You can also request our new Reseach
Tools Resource Manual.
Colon Cancer in Murine Models and Humans
This Jackson Laboratory meeting will
discuss the development and validation of
accurate preclinical rodent models and their
use in translational cancer research. To
learn more about this October 2009 meeting,
visit our website.
Expanded Sacramento operations
In
early 2009, a new, state-of-the-art JAX® Mice & Services
facility in Sacramento will begin producing
greater numbers and a wider selection of popular
JAX® Mice strains. We will
also offer more extensive breeding, in
vivo, cancer and stem cell services,
and greater customization of those services.
B6(Cg)-Tyrc-2J/J
- An ideal mouse for creating
knockouts 
B6(Cg)-Tyrc-2J/J
(000058),
or B6-albino mice, are ideal for producing novel
strains with targeted mutations. To
learn why, visit the strain
data sheet.
New JAX® Mice strains under development
You can find more information about these and other JAX® Mice strains by searching the JAX® Mice Database. If you are interested in submitting your unique research strain(s) to our international repository for mouse models, see our Strain Donation Form.
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129S/Sv-Krastm4Tyj/J (008180)
This strain carries
a point mutation (G12D) in the v-Ki-ras2 Kirsten rat sarcoma viral oncogene
homolog (Kras) gene. Homozygotes die in utero.
Cre-mediated recombination can excise the stop codon and permit the oncogenic
protein to be expressed. This strain may be used to study cancer and development.
- B10(Cg)-Cacna1aTg-5J/LetJ
(008623)
Mice heterozygous
for this semi-dominant spontaneous mutation of the calcium channel, voltage-dependent,
P/Q type, alpha 1A subunit gene have a shaky gait. They may be used to study
epilepsy and voltage-dependent calcium channels.
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B6.129P2-Gt(ROSA)26Sortm1(tTA)Roos/J (008600)
These mutant mice
may be used to generate compound mutant mice that express a tetracycline-responsive
promoter element-driven gene of interest, which can be directed to the cell
types defined by the chosen Cre recombinase expression, and turned
off by the addition of tetracycline.
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B6.129S-Cstf2ttm1Ccma/J (008370)
Male mice that are
homozygous for this targeted mutation of cleavage stimulation factor, 3' pre-RNA
subunit 2, tau (Cstf2t)
are infertile due to defective spermatogenesis. This mutant mouse strain may
be used to study polyadenylation and translational regulation of protein synthesis
during gametogenesis.
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B6.C-Cacng2stg-3J/LetJ (008624)
Homozygotes
for this spontaneous mutation of the calcium channel, voltage-dependent, gamma
subunit 2 gene have an ataxic gait. Stargazer 3J mice may be used to study epilepsy
and voltage-dependent calcium channels.
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B6.C3Bir-Cacna1atg-4J/LetJ (008622)
Homozygotes
for this spontaneous mutation of the calcium channel, voltage-dependent, P/Q
type, alpha 1A subunit gene have an ataxic gait, paroxysomal dyskinesia, and
absence seizures. Tottering 4J mice may be used to study epilepsy
and voltage-dependent calcium channels.
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B6.Cg-Dmc1tm1Jcs/JcsJ (008608)
These mice have
a targeted knockout mutation of the DMC1 dosage suppressor
of mck1 homolog, meiosis-specific homologous recombination (yeast) gene (Dmc1).
They may be used to study gametogenesis and meiosis, chromosome asynapsis,
DNA repair mechanisms, homologous recombination, and the pachytene checkpoint.
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B6.129S4-Gt(ROSA)26Sortm3(phiC31o)Sor/J (007743)
These mutant mice
express the mouse codon-optimized site-specific recombinase FC31o
from the endogenous Gt(ROSA)26Sor locus. FC31o
mediates irreversible DNA recombination at specific nonidentical pairs of sequence
sites, attB and attP.
This strain is an effective tool to generate tissue-specific targeted mutants.
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B6.FVB-Tg(TACSTD1)02Leij/J (008426)
These transgenic
mice express the human tumor-associated calcium signal transducer 1 gene (TACSTD1).
The transgene expression pattern is similar to the observed human pattern in
both normal and tumor tissue. This strain may be used to study immunological
therapies for cancer.
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B6;129P-Tg(Neurog1-cre/ESR1)1Good/J (008529)
When these Ngn1-CreERT2 transgenic
mice are bred with mice containing a loxP-flanked sequence of interest,
they produce offspring in which tamoxifen-inducible, Cre-mediated recombination
deletes the flanked sequences in Neurog1 expressing
cells. This strain may be used to study neuron development and lineage
mapping of Neurog1 expressing
cells.
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B6;C3-Tg(CAG-DsRed,-EGFP)5Gae/J (008605)
This is a double-fluorescent,
Cre-reporter strain with widespread expression of red fluorescence prior to
Cre recombinase exposure, and green fluorescence following cre-mediated
recombination in a pattern determined by cre expression.
These mice can be used to analyze complex cellular
relationships.

- BXD49/RwwJ
(007098)
BXD56/RwwJ (007104)
BXD64/RwwJ
(007109)
BXD74/RwwJ
(007118)
BXD79/RwwJ
(007123)
The BXD#/Rww recombinant
inbred strains may be used to study the genetics of behavioral phenotypes
(including alcohol and drug addiction, stress, and locomotor activity) and complex
or potentially complex physiologic phenotypes (including differences in organ
weight and bone mineral density).
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C3H;101-Dync1h1Swl/PopJ (008393)
These mice harbor
the radiation-induced Sprawling mutation of the cytoplasmic dynein heavy chain
1 gene (Dync1h1Swl). They may be used to study microtubule
motor protein function in sensory neuron degeneration, specifically in proprioceptive
sensory neurons.
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C57BL/6-Tg(HBB-cre)12Kpe/J (008314)
These transgenic
mice express Cre recombinase under the control of the human beta hemoglobin (HBB)
promoter and intron 2-enhancer fragment, and the human beta hemoglobin locus
control region (LCR). They may be used
to generate tissue-specific targeted mutants to study erythropoiesis and hematopoiesis.
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C57BL/6J-Tg(Nkx2-1-cre)2Sand/J (008661)
These Nkx2.1Cre
(or BAC-Nkx2.1-Cre) transgenic mice express cre under the control of the
Nkx2.1 promoter/enhancer regions. They may be used to generate conditional
mutations to study brain progenitor cells.
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C57BLKS/J-Cacna2d2du-2J/LetJ (008625)
Homozygotes for
the spontaneous mutation of the calcium channel, voltage-dependent, alpha 2/delta
subunit 2 gene exhibit ataxia, paroxysomal dyskinesia, and absence seizures.
Ducky 2J mice may be used to study epilepsy and voltage-dependent calcium
channels.
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NOD.129P2(B6)-Cstltm1Cptr/RclJ (008352)
This congenic NOD
strain contains a neomycin cassette disruption in exon 3 of cathepsin L (Cstltm1Cptr)
and homozygous mice are reported to be cathepsin L (Cstl)
deficient. They are insulitis free and exhibit
diabetes resistance. They may be used to identify the molecular pathways
of major lysosomal cysteine proteases (specifically cathepsin L) in immune
modulation.
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NOD.129P2(B6)-Ctsbtm1Jde/RclJ (008051)
This congenic NOD
strain contains a neomycin cassette disrupting exon 4 of cathepsin B (Ctsbtm1Jde).
Homozygotes are reportedly cathepsin B (Ctsb)
deficient. They exhibit modestly delayed
diabetes onset. They may be used to identify the molecular pathways
of major lysosomal cysteine proteases (specifically cathepsin B) in immune
modulation.
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NOD.FVB-Tg(ITGAM-DTR/EGFP)34Lan/JdkJ (008547)
Congenic NOD mice
hemizygous for a simian diphtheria toxin receptor fused with green fluorescent
protein under the control of human integrin alpha M, ITGAM, promoter (CD11b).
They are a diphtheria toxin-inducible system that transiently
depletes macrophages. They may be used to study type 1 diabetes.
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STOCK Cacnb4lh-2J/LetJ (008626)
Homozygotes for
this spontaneous mutation of the calcium channel, voltage-dependent, beta 4 subunit
gene exhibit a lethargic behavior with gait instability and the occasional seizure.
They may be used to study epilepsy and voltage-dependent calcium
channels.
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STOCK Foxa2tm1.1(rtTa)Moon/J (008335)
These Foxa2ITA/ITA
transgenic mice express the reverse tetracycline-controlled transactivator (rtTA)
protein from the forkhead box A2 (Foxa2) locus. They allow the inducible
expression of genes in cells expressing FOXA2 for cardiac and neural development
research.
Recent articles by Jackson Laboratory scientists
Anderson MG, Hawes NL, Trantow CM, Chang B, John SWM. Iris phenotypes and pigment dispersion caused by genes influencing pigmentation. Pigment
Cell Melanoma Res 2008; 21:565-78.
Bailey JS, Grabowski-Boase L, Steffy BM, Wiltshire T, Churchill
GA, Tarantino LM. Identification of quantitative trait loci for locomoter activation and anxiety using closely related inbred strains. Genes
Brain Behav 2008; 7:761-9
Blake
JA, Thomas M, Thompson JA, White R, Ziman M. Perplexing pax: from puzzle to paradigm. Dev
Dyn 2008; 237:2791-2803.
Chen J, Lu Y, Lee C-H, Li R, Leiter
EH, Mathews CE. Commonalities of genetic resistance to spontaneous autoimmune and free radical-mediated diabetes. Free
Radic Biol Med 2008; 45:1263-70.
Croker
BA, Lawson BR, Berger M, Eidenschenk C, Blasius
AL, Moresco EMY, Sovath S, Cengia L, Shultz
LD, Theofilopoulos AN, Pettersson
S, Beutler BA. Inflammation and autoimmunity
caused by a SHP1 mutation depend on IL-1, MyD88,
and a microbial trigger. Proc
Natl Acad Sci USA 2008; 105(39):15028-33.
Ghim S, Jenson AB, Bubier JA, Silva KA, Smith RS, Sundberg
JP. Cataracts in transgenic mice caused by a human papillomavirus type 18 E7 oncogene driven by KRT1-14. Exp
Molec Pathol 2008; 85:77-82.
Govoni KE, Donahue
LR, Marden C, Mohan S. Complex genetic regulation of bone mineral density and insulin-like growth factor-I in C57BL/6J-Chr #A/J/NaJ chromosome substitution strains. Physiol
Genomics 2008; 35:159-164.
Guan Y, Myers CL, Lu R, Lemischka IR, Bult
CJ, Troyanskaya OG.. A Genomewide Functional
Network for the Laboratory Mouse. PLoS
Comput Biol 2008; 4(9): e1000165.
Pang J-J, Boye SL, Kumar A, Dinculescu A, Deng W, Li J, Li Q, Rani A, Foster TC, Chang B, Hawes NL, Boatright JH, Hauswirth WW. AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation. Inv
Ophth Vis Sci 2008; 49:4278-83.
Peng Y-W, Zallocchi M, Meehan DT, Delimont D, Chang B, Hawes N, Wang W, Cosgrove D. Progressive morphological and functional defects in retinas from alpha1 integrin-null mice. Inv
Ophth Vis Sci 2008; 49(10):4647-54
Strong R, Miller RA, Astle CM, Floyd RA, Flurkey K, Hensley KL, Javors MA, Leeuwenburgh C, Nelson JF, Ongini E, Nadon NL, Warner HR, Harrison
DE. Nordihydroguaiaretic acid and aspirin increase lifespan of genetically heterogeneous male mice. Aging
Cell 2008; 7:641-50.
Stylianou IM, Langley SR, Walsh K, Chen Y, Revenu C, Paigen
B. Differences in DBA/1J and DBA/2J reveal lipid QTL genes. J
Lipid Res 2008; 49:2402-13.
Svenson
KL, Ahituv N, Durgin RS, Savage H, Magnani
PA, Foreman O, Paigen B, Peters LL. A new mouse mutant for the LDL receptor identified using ENU mutagenesis. J
Lipid Res 2008; 49:2452-62.
Thank you for your interest in JAX® Mice and Services.
Jennifer Guilmet
Regional Representative
The Jackson Laboratory
Email: jennifer.guilmet@jax.org
Tel: 1-617-780-2566
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