Dctn5-flox Mouse
Common Name
Dctn5-flox
제품 ID
S-CKO-12522
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-59288-Dctn5-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Dctn5-flox Mouse (카탈로그 번호 S-CKO-12522)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
Dctn5-flox
품종 계통계통 ID
CKOCMP-59288-Dctn5-B6J-VA
유전자명
제품 ID
S-CKO-12522
유전자 별칭
b2b315Clo, 4930427E12Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 7
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000033156
NCBI 전사체 ID
NM_021608
타겟 영역
Exon 3
유효 영역 크기
~1.1 kb
유전자 연구 개요
Dctn5, a subunit of the dynein complex involved in docking motor proteins, plays a role in microtubule-dependent trafficking. This process is associated with immune response, and studies on Dctn5 can provide insights into its role in biological processes [1].
In the Chinese tongue sole, two transcript variants of Dctn5 (dctn5_tv1 and dctn5_tv2) were identified. Dctn5_tv1 was widely distributed, especially highly expressed in immune tissues, and could be up-regulated after Vibrio harveyi challenge. Recombinant Dctn5_tv1 also showed antimicrobial activity, suggesting its involvement in the immune response to bacterial invasion [1].
In cutaneous melanoma, low expression of Dctn5 was associated with favorable overall survival, indicating its potential as a prognostic biomarker [2].
In mice with targeted inactivation of Wwtr1, which leads to glomerulocystic kidney disease, the expression of Dctn5 was decreased in the kidneys, suggesting its possible role in maintaining renal cilia integrity [3].
In double-mutant mice with Pink1 ablation and A53T-SNCA overexpression, Dctn5 was up-regulated, reflecting changes in various cellular dynamics and DNA damage [4].
In ischemic stroke, Dctn5 was part of an 8-gene signature that was highly accurate for diagnosing the disease [5].
In an in vitro study on mental disorders, knockdown of Dctn5, a bipolar disorder susceptibility gene, disrupted neuronal network physiology [6]. Also, a single-nucleotide polymorphism related to Dctn5 was associated with exercise intervention dropout in sedentary adults with overweight or obesity and cardiometabolic disease, potentially through alterations in gene expression and metabolic pathways in skeletal muscle [7].
In conclusion, Dctn5 is involved in multiple biological processes such as immune response, cancer prognosis, renal cilia integrity, and neuronal network regulation. Studies using genetic models like gene-knockout or knockdown in different organisms have revealed its significance in various disease conditions including infectious diseases, cancer, kidney diseases, mental disorders, and exercise-related phenotypes.
References:
1. Wei, Min, Xu, Wen-Teng, Li, Kun-Ming, Zhao, Fa-Zhen, Chen, Song-Lin. 2018. Cloning, characterization and functional analysis of dctn5 in immune response of Chinese tongue sole (Cynoglossus semilaevis). In Fish & shellfish immunology, 77, 392-401. doi:10.1016/j.fsi.2018.04.007. https://pubmed.ncbi.nlm.nih.gov/29635065/
2. Wang, Qiaoqi, Wang, Xiangkun, Liang, Qian, Li, Dong, Pan, Fuqiang. 2018. Prognostic Value of Dynactin mRNA Expression in Cutaneous Melanoma. In Medical science monitor : international medical journal of experimental and clinical research, 24, 3752-3763. doi:10.12659/MSM.910566. https://pubmed.ncbi.nlm.nih.gov/29864111/
3. Hossain, Zakir, Ali, Safiah Mohamed, Ko, Hui Ling, Hong, Wanjin, Hunziker, Walter. 2007. Glomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1. In Proceedings of the National Academy of Sciences of the United States of America, 104, 1631-6. doi:. https://pubmed.ncbi.nlm.nih.gov/17251353/
4. Gispert, Suzana, Brehm, Nadine, Weil, Jonas, Roeper, Jochen, Auburger, Georg. 2014. Potentiation of neurotoxicity in double-mutant mice with Pink1 ablation and A53T-SNCA overexpression. In Human molecular genetics, 24, 1061-76. doi:10.1093/hmg/ddu520. https://pubmed.ncbi.nlm.nih.gov/25296918/
5. Feng, Bing, Meng, Xinling, Zhou, Hui, Wang, Hao, Zou, Donghua. 2021. Identification of Dysregulated Mechanisms and Potential Biomarkers in Ischemic Stroke Onset. In International journal of general medicine, 14, 4731-4744. doi:10.2147/IJGM.S327594. https://pubmed.ncbi.nlm.nih.gov/34456585/
6. MacLaren, Erik J, Charlesworth, Paul, Coba, Marcelo P, Grant, Seth G N. 2011. Knockdown of mental disorder susceptibility genes disrupts neuronal network physiology in vitro. In Molecular and cellular neurosciences, 47, 93-9. doi:10.1016/j.mcn.2010.12.014. https://pubmed.ncbi.nlm.nih.gov/21440632/
7. Jiang, Rong, Collins, Katherine A, Huffman, Kim M, Siegler, Ilene C, Kraus, William E. . Genome-Wide Genetic Analysis of Dropout in a Controlled Exercise Intervention in Sedentary Adults With Overweight or Obesity and Cardiometabolic Disease. In Annals of behavioral medicine : a publication of the Society of Behavioral Medicine, 58, 363-374. doi:10.1093/abm/kaae011. https://pubmed.ncbi.nlm.nih.gov/38489667/
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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