Strain Name: |
STOCK C5ar1tm1Cge/J |
|---|---|
Stock Number: |
005676 |
Availability: | Repository- Live |
General Terms and Conditions |
| Former Name |
C.129S4(B6)-C5ar1tm1Cge/J (Changed: 02-FEB-07
) |
|
C.129S4(B6)-C5r1tm1Cge/J (Changed: 21-FEB-06
) | |
|
C.Cg-C5r1tm1Cge/J (Changed: 01-SEP-05
) | |
| Genes & Alleles | C5ar1; C5ar1tm1Cge; |
Type JAX® GEMM® Strain - Mutant Stock Additional information on JAX® GEMM® Strains. Type JAX® GEMM® Strain - Targeted Mutation Mating System Homozygote x Homozygote (Female x Male) Species laboratory mouse Donating Investigator Craig Gerard, Childrens' Hospital Boston, Harvard MS Generation ?+N1F4 (31-DEC-07) Strain Description
Mice homozygous for the targeted mutation are viable, fertile, normal in size, and do not display any gross physical or behavioral abnormalities when maintained under barrier conditions. No gene product is detected in bone marrow. The immune response of homozygous mice following inoculation or challenge has been characterized on a C57BL/6 background in a number of studies. Following intratracheal inoculation, mutant mice have impaired bacterial clearance in the lungs, associated with extensive secondary infection, despite increased neutrophil accumulation. Conversely, mutants are protected against immune-complex associated injury in the lung, peritoneum, skin, and kidney; but not against experimental autoimmune encephalomyelitis. Induced acute pancreatitis and pancreatitis-associated lung injury is more severe compared to wild type. On a BALB/c background, these mice are more resistant to dermal infection and lymph node cells have greatly increased antigen recall, as measured by interferon gamma secretion, compared to wild type. Homozygotes fail to develop airway hyper-reactivity in hapten asthma models (background not-identified). This mutant can be used to study many lung-associated diseases, immune complex associated injury, and complement innate immunity.Strain Development
A targeting vector containing a mouse phosphoglycerate kinase promoter driven neomycin resistance gene was used to replace the entire coding region of the endogenous gene. The construct was electroporated into the 129S4/SvJae-derived J1 embryonic stem (ES) cells. Correctly targeted ES cells were injected into C57BL/6 blastocysts. The resulting chimeric males were backcrossed to C57BL/6 females. Heterozygotes were next mated to C57BL/6 mice for an unknown number of generations prior to arrival at The Jackson Laboratory. Once arrived, mice were crossed at least once to BALB/cJ. The resulting heterozygous mice were then intercrossed to generate homozygous mice.
Mammalian Phenotype Terms assigned by genotype |
| Allele Symbol | C5ar1tm1Cge | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Craig Gerard | ||
| Common Name(s) | C5aR-; C5aRKO; | ||
| Mutation Made By | Craig Gerard, Childrens' Hospital Boston, Harvard MS | ||
| Strain of Origin | 129S4/SvJae | ||
| ES Cell Line Name | J1 | ||
| ES Cell Line Strain | 129S4/SvJae | ||
| Gene Symbol and Name | C5ar1, complement component 5a receptor 1 | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | C5A; C5AR; C5R1; C5r1; CD88; D7Msu1; DNA segment, Chr 7, Michigan State University 1; complement component 5, receptor 1; | ||
| Molecular Note | A PGK-neomycin resistance cassette replaced the entire coding region of the gene. Northern analysis of bone marrow cells did not detect expression in homozygous mutant mice. [MGI Ref ID J:69177] | ||
| Control | ||
|---|---|---|
| None Available | ||
| Considerations for Choosing Controls | ||
C5ar1tm1Cge
| Breeding & Husbandry | When maintaining a live colony, these mice are maintained as heterozygotes or homozygotes. For homozygous colonies, SPF conditions are recommended as mutant mice have impaired clearance of bacterial infection. |
|---|---|
| Diet Information | LabDiet® 5K52/5K67 |
Strains carrying C5ar1tm1Cge allele
006845 C.129S4(B6)-C5ar1tm1Cge/J View Strains carrying C5ar1tm1Cge (1 strain)
Congenic Nomenclature
Genetic Quality Control Annual Report
Room Number AX12
C5ar1tm1Cge related
Immunology and Inflammation Research
Autoimmunity (specific complement deficiency)
Research Tools
Immunology and Inflammation Research (genes regulating susceptibility to infectious disease and endotoxin)
Immunology and Inflammation Research (specific complement deficiency)
Selected Reference(s)
Additional ReferencesHopken UE; Lu B; Gerard NP; Gerard C. 1996. The C5a chemoattractant receptor mediates mucosal defence to infection. Nature 383(6595):86-9. [PubMed: 8779720] [MGI Ref ID J:69177]
| Strain Name: | STOCK C5ar1tm1Cge/J |
| Stock Number: | 005676 |
IMPORTANT NOTE: Prices are based on shipping destination. To view prices, select your shipping destination.
| Standard Supply | Repository-Live. A collection of over 1000 strains maintained as live colonies. Individual colonies are sized to meet current customer demand. Delivery for orders of 10 mice or less ranges on average from one to eight weeks; mice are generally shipped between four to six weeks of age with a maximum shipping age of ~nine weeks. Colony sizes do not generally support stringent age specifications for large volumes of mice; however custom orders and larger quantities of mice are easily arranged. Estimated ship dates for all orders provided within 48 hours of order placement. |
|---|---|
| Supply Notes |
Usually shipped between four and eight weeks of age. This strain is included in the Induced Mutant Resource Colony collection. Genomic DNA is available for this strain from the Mouse DNA Resource. |
| Licensing | See General Terms and Conditions below for Licensing and Use Restrictions |
| Control Information | View Control Information in Strain Details. |
For additional Licensing and Use Restrictions view the link(s) below:
- Use of MICE by companies or for-profit entities requires a license prior to shipping.
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