Scrg1-KO Mouse
Common Name
Scrg1-KO
제품 ID
S-KO-04215
Backgroud
C57BL/6NCya
품종 계통계통 ID
KOCMP-20284-Scrg1-B6N-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Scrg1-KO Mouse (카탈로그 번호 S-KO-04215)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
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.
기본 정보
품종 계통
Scrg1-KO
품종 계통계통 ID
KOCMP-20284-Scrg1-B6N-VA
유전자명
제품 ID
S-KO-04215
유전자 별칭
--
배경
C57BL/6NCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 8
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000034023
NCBI 전사체 ID
NM_009136
타겟 영역
Exon 2~3
유효 영역 크기
~3.1 kb
유전자 연구 개요
Scrg1, or scrapie responsive gene 1, encodes a highly conserved, cysteine-rich protein mainly expressed in the central nervous system, targeted to the Golgi apparatus and large dense-core vesicles/secretory granules in neurons [3,5,9]. It may be involved in the host response to stress and neuronal cell death, potentially related to autophagy [3,5]. Also, it is associated with several signaling pathways, like the MAPK pathway in macrophages [4].
In liver-related diseases, knockdown of linc-SCRG1 (a 3118-bp lncRNA) significantly reversed the effects of TGF-β1 on LX2 cells, such as inhibiting activation, promoting apoptosis, reducing proliferation, lessening invasion, and down-regulating fibrosis-related genes, suggesting its role in accelerating liver fibrosis [1]. In hepatocellular carcinoma, linc-SCRG1 acts as a ceRNA of miR26a to derepress SKP2, inducing the proliferation and migration of HCC cells [6]. In synovial inflammation, SCRG1 may be a potential therapeutic target and diagnostic marker for osteoarthritis, co-regulating immune-related pathways [2]. In macrophages, SCRG1 suppresses LPS-induced CCL22 production through ERK1/2 activation [4]. In mesenchymal stem cells, the SCRG1/BST1 axis regulates self-renewal, migration, and osteogenic differentiation potential [7,8].
In conclusion, Scrg1 has diverse functions in multiple biological processes and disease conditions. Its role in liver fibrosis, hepatocellular carcinoma, synovial inflammation, macrophage-mediated inflammation, and stem cell regulation is significant. Studies on Scrg1, especially through loss-of-function experiments, contribute to understanding disease mechanisms and may offer potential therapeutic strategies for related diseases.
References:
1. Wu, Jun-Cheng, Luo, Sheng-Zheng, Liu, Ting, Lu, Lun-Gen, Xu, Ming-Yi. 2018. linc-SCRG1 accelerates liver fibrosis by decreasing RNA-binding protein tristetraprolin. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 33, 2105-2115. doi:10.1096/fj.201800098RR. https://pubmed.ncbi.nlm.nih.gov/30226813/
2. Liu, Guoqiang, He, Guisong, Zhang, Jie, Zhang, Zhongmin, Wang, Liang. 2022. Identification of SCRG1 as a Potential Therapeutic Target for Human Synovial Inflammation. In Frontiers in immunology, 13, 893301. doi:10.3389/fimmu.2022.893301. https://pubmed.ncbi.nlm.nih.gov/35720295/
3. Dron, Michel, Bailly, Yannick, Beringue, Vincent, Laude, Hubert, Dandoy-Dron, Françoise. 2006. SCRG1, a potential marker of autophagy in transmissible spongiform encephalopathies. In Autophagy, 2, 58-60. doi:. https://pubmed.ncbi.nlm.nih.gov/16874033/
4. Inoue, Manabu, Yamada, Junko, Aomatsu-Kikuchi, Emiko, Ishisaki, Akira, Chosa, Naoyuki. 2017. SCRG1 suppresses LPS-induced CCL22 production through ERK1/2 activation in mouse macrophage Raw264.7 cells. In Molecular medicine reports, 15, 4069-4076. doi:10.3892/mmr.2017.6492. https://pubmed.ncbi.nlm.nih.gov/28440453/
5. Dron, Michel, Bailly, Yannick, Beringue, Vincent, Laude, Hubert, Dandoy-Dron, Françoise. . Scrg1 is induced in TSE and brain injuries, and associated with autophagy. In The European journal of neuroscience, 22, 133-46. doi:. https://pubmed.ncbi.nlm.nih.gov/16029203/
6. Hu, Jun-Jie, Zhou, Cui, Luo, Xin, Xu, Zi-Xin, Xu, Ming-Yi. 2021. Linc-SCRG1 accelerates progression of hepatocellular carcinoma as a ceRNA of miR26a to derepress SKP2. In Journal of experimental & clinical cancer research : CR, 40, 26. doi:10.1186/s13046-020-01825-2. https://pubmed.ncbi.nlm.nih.gov/33422101/
7. Chosa, Naoyuki, Ishisaki, Akira. 2017. Two novel mechanisms for maintenance of stemness in mesenchymal stem cells: SCRG1/BST1 axis and cell-cell adhesion through N-cadherin. In The Japanese dental science review, 54, 37-44. doi:10.1016/j.jdsr.2017.10.001. https://pubmed.ncbi.nlm.nih.gov/29629000/
8. Aomatsu, Emiko, Takahashi, Noriko, Sawada, Shunsuke, Ishisaki, Akira, Chosa, Naoyuki. 2014. Novel SCRG1/BST1 axis regulates self-renewal, migration, and osteogenic differentiation potential in mesenchymal stem cells. In Scientific reports, 4, 3652. doi:10.1038/srep03652. https://pubmed.ncbi.nlm.nih.gov/24413464/
9. Dandoy-Dron, Françoise, Griffond, Bernadette, Mishal, Zohar, Tovey, Michael G, Dron, Michel. . Scrg1, a novel protein of the CNS is targeted to the large dense-core vesicles in neuronal cells. In The European journal of neuroscience, 18, 2449-59. doi:. https://pubmed.ncbi.nlm.nih.gov/14622145/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
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