Fbln2-KO Mouse
Common Name
Fbln2-KO
제품 ID
S-KO-20512
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-14115-Fbln2-B6J-VB
상태
이 마우스 계통을 논문에서 사용할 경우, “Fbln2-KO Mouse (카탈로그 번호 S-KO-20512)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
Fbln2-KO
품종 계통계통 ID
KOCMP-14115-Fbln2-B6J-VB
유전자명
제품 ID
S-KO-20512
유전자 별칭
FIBL-2, 5730577E14Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 6
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000041544
NCBI 전사체 ID
NM_007992
타겟 영역
Exon 3~4
유효 영역 크기
~2.8 kb
유전자 연구 개요
Fbln2, also known as fibulin-2, is a secreted extracellular matrix (ECM) glycoprotein. It is essential for basement membrane integrity in mammary epithelium and is involved in multiple biological processes such as cell differentiation, proliferation, and apoptosis. It has been associated with signaling pathways like the bone morphogenic protein (BMP) pathway [1]. Fbln2 is of great biological importance as its dysregulation is linked to various diseases. Gene knockout models, such as the fbln2 knockout zebrafish line, have been crucial in studying its functions [1].
In the context of Goldenhar syndrome, a rare craniofacial malformation, fbln2 knockout zebrafish exhibited craniofacial malformations with abnormal chondrocyte morphologies. Functional studies revealed that fbln2 knockout caused abnormal chondrogenic differentiation, apoptosis, and proliferation of cranial neural crest cells (CNCCs), and downregulated the BMP signaling pathway [1]. In idiopathic pulmonary fibrosis, knockdown of FBLN2 in human lung fibroblast-derived MRC-5 cells inhibited TGF-β1-induced proliferation, migration, and fibrosis by downregulating vitronectin (VTN) [2]. In multiple sclerosis, genetic FBLN2 deficiency in the experimental autoimmune encephalomyelitis (EAE) model improved behavioral recovery by promoting oligodendrocyte maturation and enhancing remyelination [3]. In gastric cancer, overexpression of FBLN2 reduced cell proliferation and metastasis, while knockdown enhanced these processes, and it was shown to act through the TGFβ/TGIF2 axis [4].
In conclusion, Fbln2 plays essential roles in various biological processes, including craniofacial development, cell-related functions in fibrosis and cancer, and oligodendrocyte maturation. Gene knockout models, especially in zebrafish and mouse models, have significantly contributed to understanding its role in diseases such as Goldenhar syndrome, idiopathic pulmonary fibrosis, multiple sclerosis, and gastric cancer. These findings may help in developing potential screening targets and treatments for related conditions.
References:
1. Niu, Xiaomin, Zhang, Fuyu, Gu, Wei, Zhang, Bo, Chen, Xiaowei. 2024. FBLN2 is associated with Goldenhar syndrome and is essential for cranial neural crest cell development. In Annals of the New York Academy of Sciences, 1537, 113-128. doi:10.1111/nyas.15183. https://pubmed.ncbi.nlm.nih.gov/38970771/
2. Zhang, Yanju, Zhang, Weishuai, Zhang, Rui, Xia, Yunfei. 2022. Knockdown of FBLN2 suppresses TGF-β1-induced MRC-5 cell migration and fibrosis by downregulating VTN. In Tissue & cell, 81, 102005. doi:10.1016/j.tice.2022.102005. https://pubmed.ncbi.nlm.nih.gov/36608640/
3. Ghorbani, Samira, Li, Cenxiao, Lozinski, Brian M, Xue, Mengzhou, Yong, V Wee. 2024. Fibulin-2 is an extracellular matrix inhibitor of oligodendrocytes relevant to multiple sclerosis. In The Journal of clinical investigation, 134, . doi:10.1172/JCI176910. https://pubmed.ncbi.nlm.nih.gov/38743490/
4. Zhou, Ming, Mao, Xiaozhe, Shen, Kanger, Huang, Ziyi, Li, Rui. 2025. FBLN2 inhibits gastric cancer proliferation and metastasis via the TGFβ/TGIF2 pathway. In Pathology, research and practice, 269, 155899. doi:10.1016/j.prp.2025.155899. https://pubmed.ncbi.nlm.nih.gov/40168772/
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:
Cyagen문의하기
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아래 버튼을 클릭함으로써, 요청하신 콘텐츠 제공을 위해 본 양식을 통해 제출된 개인정보를 Cyagen이 저장 및 처리하는 데 동의하게 됩니다.
