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C57BL/6JCya-Apomem1/Cya
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C57BL/6JCya-Apomem1/Cya

Common Name
Apom-KO
Product ID
S-KO-10654
Backgroud
C57BL/6JCya
Strain ID
KOCMP-55938-Apom-B6J-VA
Status
Research and Development
When using this mouse strain in a publication, please cite “Apom-KO Mouse (Catalog S-KO-10654) 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
Apom-KO
Strain ID
KOCMP-55938-Apom-B6J-VA
Gene Name
Apom
Product ID
S-KO-10654
Gene Alias
G3a, NG20, 1190010O19Rik
Background
C57BL/6JCya
Gene Full Name
apolipoprotein M
Modification
Conventional knockout
NCBI ID
55938 (Mouse)
Phenotype
MGI:1930124
Chromosome
Chr 17 (Mouse)
Application
--
Datasheet
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Rare Disease Data Center >>
Strain Description
Ensembl Transcript ID
ENSMUST00000025249
NCBI Transcript ID
NM_018816
Target Region
Exon 2~5
Size of Effective Region
~1.3 kb
Overview of Gene Research
ApoM, short for apolipoprotein M, is a member of the apolipoprotein family. It is primarily expressed and secreted from the liver and kidneys. ApoM serves as the main chaperone of sphingosine-1-phosphate (S1P), a small signalling molecule involved in numerous physiologic and pathophysiologic processes. Together, the apoM-S1P axis is associated with lipid metabolism, inflammation, endothelial cell permeability, and lipid turnover [1,2].

ApoM-deficient mice display an increased activity in brown adipose tissue and a concomitant fast turnover of triglycerides, suggesting that the apoM/S1P axis plays a significant role in maintaining a balanced triglyceride metabolism [5]. In type 1 diabetes, higher apoM levels at certain time-points in the Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Interventions and Complications (EDIC) cohort were associated with an increased risk of progression to macroalbuminuria (MA) and chronic kidney disease (CKD), indicating its role in the development of nephropathy [4]. In kidney renal clear cell carcinoma (KIRC), ApoM overexpression significantly inhibited cell proliferation in vitro, suppressed epithelial-mesenchymal transition (EMT), decreased metastatic capacity, and inhibited tumor growth in vivo, potentially through the Hippo-YAP signaling pathway [3].

In conclusion, ApoM is crucial for the transport of S1P and is involved in multiple biological processes. Studies using gene-knockout or other loss-of-function models have revealed its significance in lipid metabolism, diabetes-related kidney diseases, and KIRC. These findings provide insights into potential therapeutic targets for diseases associated with ApoM dysregulation.

References:
1. Chen, Zhiyang, Hu, Min. 2020. The apoM-S1P axis in hepatic diseases. In Clinica chimica acta; international journal of clinical chemistry, 511, 235-242. doi:10.1016/j.cca.2020.10.023. https://pubmed.ncbi.nlm.nih.gov/33096030/
2. Bisgaard, Line S, Christoffersen, Christina. 2021. The apoM/S1P Complex-A Mediator in Kidney Biology and Disease? In Frontiers in medicine, 8, 754490. doi:10.3389/fmed.2021.754490. https://pubmed.ncbi.nlm.nih.gov/34722589/
3. Xu, Ting, Wei, Dan, Yang, Zhe, Xu, Zhipeng, Wang, Jianning. 2023. ApoM suppresses kidney renal clear cell carcinoma growth and metastasis via the Hippo-YAP signaling pathway. In Archives of biochemistry and biophysics, 743, 109642. doi:10.1016/j.abb.2023.109642. https://pubmed.ncbi.nlm.nih.gov/37211224/
4. Baker, Nathaniel L, Hammad, Samar M, Hunt, Kelly J, Klein, Richard L, Lopes-Virella, Maria F. . Plasma apoM Levels and Progression to Kidney Dysfunction in Patients With Type 1 Diabetes. In Diabetes, 71, 1795-1799. doi:10.2337/db21-0920. https://pubmed.ncbi.nlm.nih.gov/35554520/
5. Hajny, Stefan, Borup, Anna, Elsøe, Sara, Christoffersen, Christina. 2021. Increased plasma apoM levels impair triglyceride turnover in mice. In Biochimica et biophysica acta. Molecular and cell biology of lipids, 1866, 158969. doi:10.1016/j.bbalip.2021.158969. https://pubmed.ncbi.nlm.nih.gov/34051379/
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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