Fgf13-flox Mouse
Common Name
Fgf13-flox
제품 ID
S-CKO-02400
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-14168-Fgf13-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Fgf13-flox Mouse (카탈로그 번호 S-CKO-02400)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
Fgf13-flox
품종 계통계통 ID
CKOCMP-14168-Fgf13-B6J-VA
유전자명
제품 ID
S-CKO-02400
유전자 별칭
Fhf2, Fgf1c
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr X
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000033473
NCBI 전사체 ID
NM_010200
타겟 영역
Exon 3
유효 영역 크기
~1.0 kb
유전자 연구 개요
Fgf13, a non-canonical, non-secreted fibroblast growth factor, is involved in multiple biological processes. It interacts with microtubules and is associated with pathways related to calcium signaling, ion channel regulation, and immune-related functions. Genetic models, such as KO and CKO mouse models, have been crucial for studying its functions [1,2,6].
In heart failure models, Fgf13 deficiency alleviates cardiac dysfunction by improving abnormal calcium signaling through inhibiting increased microtubule stability [1]. In dorsal root ganglion neurons, conditional knockout of Fgf13 impairs scratching behaviors in acute and chronic itch models, as it selectively regulates TRPV1 function via microtubule-stabilizing effect [2]. In AML patients, low Fgf13 expression is related to prognosis, and overexpression in xenograft models inhibits AML cell growth [3]. In diabetic nephropathy, endothelial-specific deletion of Fgf13 alleviates damage by improving mitochondrial homeostasis [4]. Obesity-induced Fgf13 in adipose tissue impairs energy and glucose homeostasis [5]. Interneuron-targeted deletion of Fgf13 leads to seizures and affects K⁺ channel currents [6]. Stable Fgf13 depletion in triple-negative breast cancer cells restricts metastasis [7]. Loss of Fgf13 in mouse DRG neurons impairs histamine-induced scratching behavior [8]. Fgf13 up-regulation in cardiac hypertrophy has a deteriorating role, and its deficiency inhibits NF-κB activation [9]. Cardiac Fgf13 knockdown alleviates fibrosis by modulating microtubule stabilization and ROCK signaling pathway [10].
In conclusion, Fgf13 plays essential roles in various biological processes including calcium homeostasis, itch sensation, cancer development, metabolic regulation, and neuronal excitability. Gene knockout and conditional knockout mouse models have significantly contributed to understanding its functions in heart failure, leukemia, diabetic nephropathy, metabolic diseases, epilepsy, and breast cancer, providing potential therapeutic targets for these diseases.
References:
1. Zhao, Ran, Yan, Yingke, Dong, Yiming, Gu, Guoqiang, Wang, Chuan. 2024. FGF13 deficiency ameliorates calcium signaling abnormality in heart failure by regulating microtubule stability. In Biochemical pharmacology, 225, 116329. doi:10.1016/j.bcp.2024.116329. https://pubmed.ncbi.nlm.nih.gov/38821375/
2. Dong, Zi-Shan, Zhang, Xue-Rou, Xue, Da-Zhong, Zhang, Hai-Lin, Wang, Chuan. . FGF13 enhances the function of TRPV1 by stabilizing microtubules and regulates acute and chronic itch. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 38, e23661. doi:10.1096/fj.202400096R. https://pubmed.ncbi.nlm.nih.gov/38733310/
3. Li, Ran, Xue, Kai, Li, Junmin. 2022. FGF13 suppresses acute myeloid leukemia by regulating bone marrow niches. In Frontiers of medicine, 16, 896-908. doi:10.1007/s11684-022-0944-z. https://pubmed.ncbi.nlm.nih.gov/36053411/
4. Sun, Jia, Guan, Xueqiang, Niu, Chao, Jin, Litai, Cong, Weitao. . FGF13-Sensitive Alteration of Parkin Safeguards Mitochondrial Homeostasis in Endothelium of Diabetic Nephropathy. In Diabetes, 72, 97-111. doi:10.2337/db22-0231. https://pubmed.ncbi.nlm.nih.gov/36256844/
5. Naderi, Jamal, Johnson, Amanda Kelsey, Thakkar, Himani, Pitt, Geoffrey S, Chaurasia, Bhagirath. 2025. Ceramide-induced FGF13 impairs systemic metabolic health. In Cell metabolism, 37, 1206-1222.e8. doi:10.1016/j.cmet.2025.03.002. https://pubmed.ncbi.nlm.nih.gov/40169001/
6. Lin, Susan, Gade, Aravind R, Wang, Hong-Gang, Rajadhyaksha, Anjali M, Pitt, Geoffrey S. 2024. Interneuron FGF13 regulates seizure susceptibility via a sodium channel-independent mechanism. In bioRxiv : the preprint server for biology, , . doi:10.1101/2024.04.18.590019. https://pubmed.ncbi.nlm.nih.gov/38659789/
7. Johnstone, Cameron N, Pattison, Andrew D, Harrison, Paul F, Anderson, Robin L, Beilharz, Traude H. 2020. FGF13 promotes metastasis of triple-negative breast cancer. In International journal of cancer, 147, 230-243. doi:10.1002/ijc.32874. https://pubmed.ncbi.nlm.nih.gov/31957002/
8. Dong, Fei, Shi, Haixiang, Yang, Liu, Bao, Lan, Zhang, Xu. 2020. FGF13 Is Required for Histamine-Induced Itch Sensation by Interaction with NaV1.7. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 40, 9589-9601. doi:10.1523/JNEUROSCI.0599-20.2020. https://pubmed.ncbi.nlm.nih.gov/33172979/
9. Sun, Jia, Niu, Chao, Ye, Weijian, Cong, Weitao, Li, Xiaokun. 2020. FGF13 Is a Novel Regulator of NF-κB and Potentiates Pathological Cardiac Hypertrophy. In iScience, 23, 101627. doi:10.1016/j.isci.2020.101627. https://pubmed.ncbi.nlm.nih.gov/33089113/
10. Wang, Cong, Wang, Xiangchong, Zhang, Yiyi, Gu, Guoqiang, Wang, Chuan. . Inducible Fgf13 ablation alleviates cardiac fibrosis via regulation of microtubule stability. In Acta biochimica et biophysica Sinica, 56, 1802-1812. doi:10.3724/abbs.2024075. https://pubmed.ncbi.nlm.nih.gov/38818580/
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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