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C57BL/6JCya-Stx11em1/Cya
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C57BL/6JCya-Stx11em1/Cya

Common Name
Stx11-KO
Product ID
S-KO-14505
Backgroud
C57BL/6JCya
Strain ID
KOCMP-74732-Stx11-B6J-VA
Status
Research and Development
When using this mouse strain in a publication, please cite “Stx11-KO Mouse (Catalog S-KO-14505) were purchased from Cyagen.”
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The standard delivery applies for a guaranteed minimum of three heterozygous carriers. Breeding services for homozygous carriers and/or specified sex are available.
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KO Models
Basic Information
Strain Name
Stx11-KO
Strain ID
KOCMP-74732-Stx11-B6J-VA
Gene Name
Stx11
Product ID
S-KO-14505
Gene Alias
5830405C08Rik
Background
C57BL/6JCya
NCBI ID
74732 (Mouse)
Modification
Conventional knockout
Chromosome
Chr 10 (Mouse)
Phenotype
MGI:1921982
Datasheet
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Application
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Rare Disease Data Center >>
Strain Description
Ensembl Transcript ID
ENSMUST00000042861
NCBI Transcript ID
NM_029075
Target Region
Exon 3
Size of Effective Region
~3.1 kb
Overview of Gene Research
Stx11, a member of the SNARE family, is generally expressed in immune cells. It mediates membrane fusion events, playing a role in processes like cytotoxic granule exocytosis at immunological synapses of CD8 T or NK cells, and is involved in pathways related to lipid metabolism, cell proliferation, and autophagy [3,4,5]. Genetic models, such as gene-knockout (KO) mouse models, are valuable for studying its functions.

In KO mouse models, restricting fatty acid supply, blocking fatty acid uptake, or inhibiting Stx11 palmitoylation attenuates muscle regeneration. This shows that dynamic palmitoylation of Stx11 controls injury-induced fatty acid uptake in muscle stem cells to promote muscle regeneration [1]. In the context of pulmonary fibrosis, overexpression of Stx11 in mice alleviates the condition by inhibiting fibroblast activation via the PI3K/AKT/mTOR pathway [2]. In Stx11-deficient mice, there is impaired CD4 T cell help for B cells, disrupted germinal center formation, reduced isotype class switching, and low antibody avidity, indicating its role in humoral immunity [5].

In conclusion, Stx11 is crucial for multiple biological processes. Its functions in muscle regeneration, pulmonary fibrosis, and humoral immunity have been revealed through model-based research, especially KO mouse models. These findings contribute to understanding the underlying mechanisms of related diseases and may provide potential therapeutic targets for conditions like muscle injury, pulmonary fibrosis, and immunodeficiency-related disorders.

References:
1. Wang, Juan, Li, Dong-Lin, Zheng, Lang-Fan, Li, Peng, Zhao, Tong-Jin. 2024. Dynamic palmitoylation of STX11 controls injury-induced fatty acid uptake to promote muscle regeneration. In Developmental cell, 59, 384-399.e5. doi:10.1016/j.devcel.2023.12.005. https://pubmed.ncbi.nlm.nih.gov/38198890/
2. Huang, Guichuan, Yang, Xiangsheng, Yu, Qingyang, Zhong, Nanshan, Tang, Xiao Xiao. 2024. Overexpression of STX11 alleviates pulmonary fibrosis by inhibiting fibroblast activation via the PI3K/AKT/mTOR pathway. In Signal transduction and targeted therapy, 9, 306. doi:10.1038/s41392-024-02011-y. https://pubmed.ncbi.nlm.nih.gov/39523374/
3. Canna, Scott W, Marsh, Rebecca A. . Pediatric hemophagocytic lymphohistiocytosis. In Blood, 135, 1332-1343. doi:10.1182/blood.2019000936. https://pubmed.ncbi.nlm.nih.gov/32107531/
4. Zhang, Gaojian, Han, Jianxiong, Wang, Lili, Ge, Honghua, Yang, Xingyuan. 2022. The vesicular transporter STX11 governs ATGL-mediated hepatic lipolysis and lipophagy. In iScience, 25, 104085. doi:10.1016/j.isci.2022.104085. https://pubmed.ncbi.nlm.nih.gov/35372814/
5. Kögl, Tamara, Chang, Hsin-Fang, Staniek, Julian, Aichele, Peter, Ammann, Sandra. 2024. Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect. In The Journal of experimental medicine, 221, . doi:10.1084/jem.20221122. https://pubmed.ncbi.nlm.nih.gov/38722309/
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
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Global Antibody Drug Industry Development BlueBook (Frost & Sullivan)
Key Insights
The industry is undergoing a rapid transformation driven by next-generation modalities, globalized markets, and upstream technological innovations.
  • Market Structural Shift: Monoclonal antibodies drive steady growth, but ADCs and bispecifics are rapidly accelerating, reshaping the market with higher-value innovations.
  • Chinese Market Globalization: China is actively expanding globally, evidenced by a surge in high-value cross-border license-out deals.
  • Technology-Driven Efficiency: Advanced discovery engines—exemplified by Cyagen's HUGO-Ab platform and AI algorithms—are streamlining candidate screening, optimizing molecular design, and localizing the upstream supply chain.
  • Oncology-Focused Innovation: R&D pipelines remain heavily concentrated on high-incidence malignancies like non-small cell lung cancer, utilizing complex modalities to combat clinical resistance.
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