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C57BL/6JCya-Tsnem1flox/Cya
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C57BL/6JCya-Tsnem1flox/Cya

Common Name
Tsn-flox
Product ID
S-CKO-06468
Backgroud
C57BL/6JCya
Strain ID
CKOCMP-22099-Tsn-B6J-VA
Status
Research and Development
When using this mouse strain in a publication, please cite “Tsn-flox Mouse (Catalog S-CKO-06468) 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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Basic Information
Strain Name
Tsn-flox
Strain ID
CKOCMP-22099-Tsn-B6J-VA
Gene Name
Tsn
Product ID
S-CKO-06468
Gene Alias
2610034C24Rik, C3PO, TB-RBP
Background
C57BL/6JCya
Gene Full Name
--
Modification
Conditional knockout
NCBI ID
22099 (Mouse)
Phenotype
MGI:109263
Chromosome
Chr 1 (Mouse)
Application
--
Datasheet
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Rare Disease Data Center >>
Strain Description
Ensembl Transcript ID
ENSMUST00000027623
NCBI Transcript ID
NM_011650
Target Region
Exon 2~3
Size of Effective Region
~2.1 kb
Overview of Gene Research
Tsn, or Tudor-staphylococcal/micrococcal-like nuclease, is involved in miRNA decay. It promotes the degradation of miRNAs containing CA and/or UA dinucleotides, which is a process known as TumiD [1]. This function potentially impacts gene expression regulation as miRNAs are key regulators of protein-encoding transcripts.

Cellular TumiD requires the ATP-dependent RNA helicase UPF1, and UPF1 can dissociate miRNAs from their mRNA targets, making them more susceptible to TumiD. In T24 human urinary bladder cancer cells, UPF1 augments the degradation of about 50% of candidate TumiD targets. UPF1-augmented TumiD promotes the invasion of T24 cells by degrading anti-invasive miRNAs and up-regulating proinvasive proteins [1].

In conclusion, Tsn plays a crucial role in miRNA decay, which can influence gene expression. Its function in promoting the invasion of bladder cancer cells through miRNA-mediated pathways, as revealed by in vitro studies on T24 cells, provides insights into cancer-related biological processes. Understanding Tsn's role in miRNA decay may offer new perspectives on gene regulation and potential therapeutic targets in cancer.

References:
1. Elbarbary, Reyad A, Miyoshi, Keita, Hedaya, Omar, Myers, Jason R, Maquat, Lynne E. 2017. UPF1 helicase promotes TSN-mediated miRNA decay. In Genes & development, 31, 1483-1493. doi:10.1101/gad.303537.117. https://pubmed.ncbi.nlm.nih.gov/28827400/
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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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