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Strain Name: |
C.129P2-Cxcr6tm1Litt/J |
Stock Number: |
005700 |
Availability:
| Repository-Cryopreserved |
Product Information
Strain Details
| Type |
JAX® GEMM® Strain -
Congenic |
| Additional information on
JAX® GEMM® Strains. |
| Type |
JAX® GEMM® Strain -
Mutant Strain |
| Type |
JAX® GEMM® Strain -
Targeted Mutation |
| Species | laboratory mouse |
| Donating Investigator | Dan Littman, New York University Medical Center |
| Generation | N12F?+N1p
(04-DEC-05)
|
|
|
Strain Description
Mice homozygous for this EGFP "knock-in" are viable, fertile, normal in size, and do not display any behavioral abnormalities when maintained under barrier conditions. Lymph nodes and spleen show no endogenous gene expression. Lymphocytes from heterozygotes, but not homozygotes, show endogenous ligand binding. EGFP expression is restricted to spleen and lymph nodes, specifically activated/memory T cells, with a slightly higher intensity in homozygotes. Homozygous null mice show decreased EGFP+ CD1d-reactive NKT patrolling efficiency and decreased severity of induced acute hepatitis, while heterozygotes and wildtype mice show no differences. This mutant may be useful in studies of hepatitis, HIV, SIV, fluorescent T cell tracking, and various immune responses.
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. 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.
Strain Development
A targeting vector containing an enhanced green fluorescent protein (EGFP)/SV40 poly(A)n cassette with a downstream loxP-flanked neomycin resistance gene and herpes simplex virus thymidine kinase was used to replace the endogenous coding sequence. The construct was electroporated into the 129P2/OlaHsd-derived E14 embryonic stem (ES) cells. Correctly targeted ES cells were transiently transfected with a Cre recombinase-expressing vector before being injected into C57BL/6 blastocysts. The resulting chimeric mice were bred to BALB/c mice. Heterozygotes were backcrossed to BALB/c mice for 12 generations before being made homozygous.
Mammalian Phenotype Terms assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Cxcr6tm1Litt/Cxcr6tm1Litt
involves: 129P2/OlaHsd * C57BL/6
- normal phenotype
- no abnormal phenotype detected
(MGI Ref ID J:104242)
- in a specific pathogen-free environment mice are viable with normal immune cell populations, T cell proliferation, and IgM and IgG1 levels
|
Gene & Allele Details
| Allele Symbol |
Cxcr6tm1Litt |
| Allele Name |
targeted mutation 1, Daniel Littman |
| Common Name(s) |
Bonzo-;
Bz-;
Cxcr6tm1Unu;
cxcr6gfp;
|
| Mutation Made By | Dan Littman, New York University Medical Center |
| Strain of Origin | 129P2/OlaHsd |
| ES Cell Line Name | E14 |
| ES Cell Line Strain | 129P2/OlaHsd |
| Site of Expression | EGFP expression mimics endogenous gene expression and is detected in the spleen and lymph nodes, specifically activated/memory T cells. |
| Gene Symbol and Name |
Cxcr6, chemokine (C-X-C motif) receptor 6 |
| Chromosome |
9 |
| Gene Common Name(s) |
BB217514;
BONZO;
CD186;
STRL33;
TYMSTR;
expressed sequence BB217514;
|
| Molecular Note |
The coding sequence was replaced with an EGFP. RT-PCR failed to detect transcript in mutants. Strong GFP expression was detected in spleen and lymphoid nodes. [MGI Ref ID J:104242]
[MGI Ref ID J:131925]
|
Control Information
Genotyping Protocols
Cxcr6tm1Litt
Colony Maintenance
| Breeding & Husbandry | When maintaining a live colony, these mice are maintained as homozygotes. |
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View Fluorescent Protein Strains (145 strains)
Strains carrying Cxcr6tm1Litt allele
View Strains carrying Cxcr6tm1Litt (1 strain)
Additional Web Information
Congenic Nomenclature
Fluorescent Proteins/lacZ Systems
Research Applications
This mouse can be used to support research in many areas including:
Immunology and Inflammation Research
Mechanisms of HIV Infection
Research Tools
Fluorescent Proteins
Genetics Research
(Tissue/Cell Markers: T cell specific surface marker)
Immunology and Inflammation Research
(AIDS research tool)
Immunology and Inflammation Research
(T cell specific surface marker)
References
Selected Reference(s)
Unutmaz D; Xiang W; Sunshine MJ; Campbell J; Butcher E; Littman DR. 2000. The primate lentiviral receptor Bonzo/STRL33 is coordinately regulated with CCR5 and its expression pattern is conserved between human and mouse. J Immunol
165(6):3284-92.
[PubMed: 10975845]
[MGI Ref ID J:104242]
Additional References
Price and Supply Information
| Strain Name: |
C.129P2-Cxcr6tm1Litt/J |
| Stock Number: |
005700 |
Price Details
IMPORTANT NOTE: Prices are based on shipping destination.
The shipping destinations are:
*Pricing for Shipping Destination selected:
USA, Canada and Mexico
| Price(s) in US dollars ($) | |
| Cryorecovery Fee | $1900.00 | | | |
| Cryopreserved Embryos Fee | $1600.00 | | | |
Supply Details
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information. |
| Supply Notes |
Cryopreserved Embryos This strain is also available as cryopreserved embryos from our Repository. Orders for cryopreserved embryos are supplied subject to a signed agreement that must be returned to the Customer Service Department after order placement. 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 from our repository, please visit our Cryopreserved Embryos web page.
Cryorecovery - Standard. The recovery process begins when a signed agreement form is returned to the Customer Service Department after order placement. Although results vary by strain, at least two males and two females (two pairs) will be provided, typically within 15 weeks of our receipt of the signed agreement form. If the first recovery attempt is unsuccessful or only one pair is recovered, a second recovery will be done, extending the delivery time to approximately 25 weeks. At least one member of each pair will be of known genotype and will carry the mutation if it is a mutant strain. Please note that pairs may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation of the strain. Mating schemes are sometimes modified for successful cryopreservation. Price represents a repository maintenance fee, which includes the cost of recovery of the strain from the cryopreservation resource and the periodic replacement of the frozen embryos used for recovery.
Cryorecovery to establish a Dedicated Supply for greater quantities of mice. One to two pairs will be recovered to establish a Dedicated Supply of mice. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services: Tel: 1-800-422-6423 or 1-207-288-5845; Email: jaxservices@jax.org.
This strain is included in the Induced Mutant Resource Colony collection.
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Effective September 26, 2007: License Requirements for Strains using Cre-lox Technology only apply in Canada, see Licenses for Strains using Cre-lox Technology.
For additional Licensing and Use Restrictions view the link(s) below:
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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
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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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