C57BL/6JCya-Vamp5em1flox/Cya
Common Name:
Vamp5-flox
Product ID:
S-CKO-19292
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
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Basic Information
Strain Name
Vamp5-flox
Strain ID
CKOCMP-53620-Vamp5-B6J-VA
Gene Name
Product ID
S-CKO-19292
Gene Alias
Camp
Background
C57BL/6JCya
NCBI ID
Modification
Conditional knockout
Chromosome
6
Phenotype
Document
Application
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Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Vamp5em1flox/Cya mice (Catalog S-CKO-19292) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000101285
NCBI RefSeq
NM_016872
Target Region
Exon 2~3
Size of Effective Region
~1.7 kb
Detailed Document
Overview of Gene Research
VAMP5, short for Vesicle-associated membrane protein 5, is a member of the SNARE protein family. SNARE proteins generally regulate the docking and fusion of membrane vesicles within cells. VAMP5 is involved in multiple biological processes such as exosome release, phagocytosis, and membrane trafficking in various tissues [1,2,5]. It participates in exosome release from multivesicular bodies (MVBs) to the plasma membrane, and also plays a role in Fcγ receptor-mediated phagosome formation in macrophages [1,2].
VAMP5 knockout (KO) mice showed a low birth rate, low body weight, and often died around birth. Anatomical analysis of these KO mice revealed duplication of the ureter in viable ones and insufficient lung expansion in dead ones, indicating its importance in the development of the urinary and respiratory systems [3].
In conclusion, VAMP5 is crucial for membrane-related biological processes like exosome release and phagosome formation. The VAMP5 KO mouse model has demonstrated its significance in the development of the urinary and respiratory systems. Its potential as a biomarker in diseases like tuberculosis and its association with diseases such as Hirschsprung disease further highlight its importance in disease-related research [3,4,6,7].
References:
1. Matsui, Takahide, Sakamaki, Yuriko, Hiragi, Shu, Fukuda, Mitsunori. 2023. VAMP5 and distinct sets of cognate Q-SNAREs mediate exosome release. In Cell structure and function, 48, 187-198. doi:10.1247/csf.23067. https://pubmed.ncbi.nlm.nih.gov/37704453/
2. Sakurai, Chiye, Yamashita, Natsumi, Azuma, Kento, Hatsuzawa, Kiyotaka. 2024. VAMP5 promotes Fcγ receptor-mediated phagocytosis and regulates phagosome maturation in macrophages. In Molecular biology of the cell, 35, ar44. doi:10.1091/mbc.E23-04-0149. https://pubmed.ncbi.nlm.nih.gov/38265888/
3. Ikezawa, Maiko, Tajika, Yuki, Ueno, Hitoshi, Inoue, Naokazu, Yorifuji, Hiroshi. 2018. Loss of VAMP5 in mice results in duplication of the ureter and insufficient expansion of the lung. In Developmental dynamics : an official publication of the American Association of Anatomists, 247, 754-762. doi:10.1002/dvdy.24618. https://pubmed.ncbi.nlm.nih.gov/29330887/
4. Arya, Rakesh, Shakya, Hemlata, Chaurasia, Reetika, Haque, Md Azizul, Kim, Jong-Joo. 2024. Exploring the Role of Extracellular Vesicles in the Pathogenesis of Tuberculosis. In Genes, 15, . doi:10.3390/genes15040434. https://pubmed.ncbi.nlm.nih.gov/38674369/
5. Takahashi, Maiko, Tajika, Yuki, Khairani, Astrid Feinisa, Murakami, Tohru, Yorifuji, Hiroshi. 2012. The localization of VAMP5 in skeletal and cardiac muscle. In Histochemistry and cell biology, 139, 573-82. doi:10.1007/s00418-012-1050-0. https://pubmed.ncbi.nlm.nih.gov/23180306/
6. Shin, J-G, Kim, D-Y, Seo, J-M, Kim, J-H, Shin, H D. 2016. Potential association of VAMP5 polymorphisms with total colonic aganglionosis in Hirschsprung disease. In Neurogastroenterology and motility, 28, 1055-63. doi:10.1111/nmo.12807. https://pubmed.ncbi.nlm.nih.gov/26970437/
7. Zhao, Jinglu, Xie, Xiaoli, Yao, Yuxiao, Xia, Huimin, Zhang, Yan. . Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children. In Aging, 10, 689-700. doi:10.18632/aging.101423. https://pubmed.ncbi.nlm.nih.gov/29695640/
Quality Control Standard
Sperm Test
Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.
Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.
Environmental Standards:SPF
Available Region:Global
Source:Cyagen