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Rag2 KO Mouse
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Rag2 KO Mouse
제품명
Rag2 KO Mouse
제품 ID
C001324
품종 계통
C57BL/6JCya-Rag2em1/Cya
Backgroud
C57BL/6JCya
상태
이 마우스 계통을 논문에서 사용할 경우, “Rag2 KO Mouse (카탈로그 번호 C001324)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
Other Immunodeficient Mice
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
가격 문의
Other Immunodeficient Mice
기본 정보
검증 데이터
관련 자료
기본 정보
유전자명
유전자 별칭
Rag-2
NCBI ID
염색체
Chr 2
MGI ID
Datasheet
품종 계통 설명
The RAG2 gene encodes a protein that, together with the RAG1 protein, forms the RAG complex, playing a crucial role in V(D)J recombination during the maturation of B and T cells. During V(D)J recombination, the RAG complex attaches to the recombination signal sequences (RSS) located adjacent to V, D, or J segments in the DNA. The RAG complex cuts the DNA between the signal sequences and the segments, allowing the segments to separate and move to different regions of the genome. This process occurs repeatedly in B and T cells, arranging the V, D, and J segments in various combinations. The resulting protein diversity provides a broader capability to recognize foreign invaders, allowing the body to combat infections effectively. RAG2 is essential in V(D)J recombination, not only catalyzing the reaction but also regulating it by controlling access to specific loci. A lack of functional RAG2 protein can also lead to severe combined immunodeficiency (SCID). In mice, deleting the Rag2 gene results in the absence of V(D)J recombination, blocking the differentiation, development, and maturation of T and B cells, which lose their normal functions, leading to a SCID-like phenotype.
Rag2 KO mice are Rag2 gene knockout (KO) models. Homozygous Rag2 KO mice develop normally and are fertile but do not produce mature T and B cells. They can be used in research on immune system deficiencies, cancer, toxicology, and xenotransplantation.
변형 전략
The mouse Rag2 gene is located on chromosome 2 and contains three exons. Both the start and stop codons are located on exon 3. The Rag2 gene knockout was achieved by targeting exon 3 using gene editing technology.

Figure 1. Diagram of the gene editing strategy for the generation of Rag2 KO mice.
검증 데이터
1. Flow cytometry detection of T and B cells in peripheral blood, thymus, and spleen
Peripheral blood, thymus, and spleen from Rag2 KO mice were subjected to representative flow cytometry immunophenotyping analysis and statistical comparison of their T and B cell composition. The results indicate that Rag2 KO mice show almost complete absence of B cells (CD3-CD19+) and T cells (CD3+CD19-) in peripheral blood, thymus, and spleen.

Figure 2. Detection of T and B cells in peripheral blood (PB), thymus, and spleen of Rag2 KO mice.
2. Flow cytometry detection of myeloid cells in peripheral blood and spleen
(1)Detection of monocytes, macrophages, neutrophils, and dendritic cells (DC) in peripheral blood
The results show a significant increase in Lin- cells (excluding T, B, and NK cells) in the peripheral blood of Rag2 KO mice compared to wild-type mice. There is no significant difference in the proportions of monocytes, macrophages, and dendritic cells (DC), but an increase in the proportion of neutrophils.


Figure 3. Flow cytometry results of myeloid cells in the peripheral blood of 6-week-old female wild-type (WT) and Rag2 KO mice (n=3).
(2)Detection of monocytes, macrophages, neutrophils, and dendritic cells (DC) in the spleen
The results show a significant increase in Lin-cells (excluding T, B, and NK cells) in the spleens of Rag2 KO mice compared to wild-type mice. There is no significant difference in the proportion of monocytes, whereas the proportions of macrophages, neutrophils, and dendritic cells (DC) are significantly increased.


Figure 4. Flow cytometry results of myeloid cells in the spleens of 6-week-old female wild-type (WT) and Rag2 KO mice (n=3).
관련 자료
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