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C57BL/6JCya-Pabpc4em1/Cya
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C57BL/6JCya-Pabpc4em1/Cya

Common Name
Pabpc4-KO
Product ID
S-KO-06360
Backgroud
C57BL/6JCya
Strain ID
KOCMP-230721-Pabpc4-B6J-VB
Status
Research and Development
When using this mouse strain in a publication, please cite “Pabpc4-KO Mouse (Catalog S-KO-06360) were purchased from Cyagen.”
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Basic Information
Strain Name
Pabpc4-KO
Strain ID
KOCMP-230721-Pabpc4-B6J-VB
Gene Name
Pabpc4
Product ID
S-KO-06360
Gene Alias
--
Background
C57BL/6JCya
Gene Full Name
poly(A) binding protein, cytoplasmic 4
Modification
Conventional knockout
NCBI ID
230721 (Mouse)
Phenotype
MGI:2385206
Chromosome
Chr 4 (Mouse)
Application
--
Datasheet
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Rare Disease Data Center >>
Strain Description
Ensembl Transcript ID
ENSMUST00000080178
NCBI Transcript ID
NM_130881
Target Region
Exon 2~3
Size of Effective Region
~3.8 kb
Overview of Gene Research
Pabpc4, short for poly(A)-binding protein cytoplasmic 4, is an RNA-processing protein. It belongs to the family of cytoplasmic poly(A)-binding proteins (PABPs) and plays a crucial role in promoting gene expression by enhancing translation and mRNA stability. It is involved in multiple biological processes such as energy metabolism, cell differentiation, and antiviral defense [1-3].

In the context of coronavirus replication, Pabpc4 can be regulated by transcription factor SP1 and broadly inhibits the replication of coronaviruses from four genera. It targets the nucleocapsid (N) protein, recruits the E3 ubiquitin ligase MARCH8/MARCHF8 for ubiquitination of the N protein. The ubiquitinated N protein is then recognized by the cargo receptor NDP52/CALCOCO2 and delivered to autolysosomes for degradation, impairing viral proliferation [1,4]. In 3T3-L1 pre-adipocytes, knockdown experiments suggest that Pabpc4 contributes to regulating differentiation and energy metabolism [2]. In C2C12 and MEF cells, silencing of Pabpc4 induces an oxidative phenotype, as it increases the ubiquitination and degradation of NCoR1, derepressing PPAR-regulated genes [3].

In summary, Pabpc4 is essential for gene expression regulation and is involved in various biological processes. Its role in inhibiting coronavirus replication, regulating adipocyte differentiation and energy metabolism, as well as modulating the metabolic stress response has been revealed through functional studies including knockdown and silencing experiments. These findings contribute to our understanding of antiviral strategies, diabetes-related metabolic processes, and potential treatments for metabolic diseases [1-4].

References:
1. Jiao, Yajuan, Kong, Ning, Wang, Hua, Tong, Guangzhi, Shan, Tongling. 2021. PABPC4 Broadly Inhibits Coronavirus Replication by Degrading Nucleocapsid Protein through Selective Autophagy. In Microbiology spectrum, 9, e0090821. doi:10.1128/Spectrum.00908-21. https://pubmed.ncbi.nlm.nih.gov/34612687/
2. Tang, Haibo, Wang, Jie, Deng, Peizhi, Zhu, Shaihong, Lu, Yao. 2023. Transcriptome-wide association study-derived genes as potential visceral adipose tissue-specific targets for type 2 diabetes. In Diabetologia, 66, 2087-2100. doi:10.1007/s00125-023-05978-5. https://pubmed.ncbi.nlm.nih.gov/37540242/
3. Oliveira, A G, Oliveira, L D, Cruz, M V, Auwerx, J, Silveira, L R. 2023. Interaction between poly(A)-binding protein PABPC4 and nuclear receptor corepressor NCoR1 modulates a metabolic stress response. In The Journal of biological chemistry, 299, 104702. doi:10.1016/j.jbc.2023.104702. https://pubmed.ncbi.nlm.nih.gov/37059182/
4. Zhao, Chenchen, Qin, Yan, Huang, Haixin, Lan, Tian, Sun, Wenchao. 2025. PABPC4 Inhibits SADS-CoV Replication by Degrading the Nucleocapsid Protein Through Selective Autophagy. In Veterinary sciences, 12, . doi:10.3390/vetsci12030257. https://pubmed.ncbi.nlm.nih.gov/40266995/
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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