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C57BL/6JCya-Hs1bp3em1/Cya
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C57BL/6JCya-Hs1bp3em1/Cya

Common Name
Hs1bp3-KO
Product ID
S-KO-11111
Backgroud
C57BL/6JCya
Strain ID
KOCMP-58240-Hs1bp3-B6J-VA
Status
Research and Development
When using this mouse strain in a publication, please cite “Hs1bp3-KO Mouse (Catalog S-KO-11111) were purchased from Cyagen.”
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Basic Information
Strain Name
Hs1bp3-KO
Strain ID
KOCMP-58240-Hs1bp3-B6J-VA
Gene Name
Hs1bp3
Product ID
S-KO-11111
Gene Alias
--
Background
C57BL/6JCya
Gene Full Name
HCLS1 binding protein 3
Modification
Conventional knockout
NCBI ID
58240 (Mouse)
Phenotype
MGI:1913224
Chromosome
Chr 12 (Mouse)
Application
--
Datasheet
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Strain Description
Ensembl Transcript ID
ENSMUST00000020927
NCBI Transcript ID
NM_021429
Target Region
Exon 2~3
Size of Effective Region
~3.9 kb
Overview of Gene Research
Hs1bp3, also known as HCLS1 binding protein 3, is a protein-coding gene with significant functions in multiple biological processes. It contains several important segments like a PX domain, a leucine zipper, and may be involved in lymphocyte activation [5]. It also has a role in regulating autophagy, a crucial membrane trafficking and intracellular degradation process [1,3,4].

In autophagy, HS1BP3 acts as a negative regulator of autophagosome formation. Depletion of HS1BP3 in human cells and zebrafish increases the formation of LC3-positive autophagosomes [1,4]. HS1BP3 localizes to autophagosome precursors and binds phosphatidic acid (PA) through its PX domain. When HS1BP3 is depleted, the total cellular PA content is upregulated due to increased activity of PLD1 and its localization to ATG16L1-positive membranes, suggesting HS1BP3 regulates autophagy by modulating PA content in autophagosome precursor membranes [1,3,4]. In hepatocellular carcinoma, high expression of HS1BP3 is associated with poor prognosis, and its silencing inhibits proliferation, invasion, and migration of HCC cells. Estrogen receptor 1 (ESR1) can inhibit HCC proliferation and improve prognosis by interacting with the HS1BP3 promoter [2].

In conclusion, HS1BP3 has a negative regulatory function in autophagy through modulating membrane lipids, and it promotes hepatocellular carcinoma progression. The study of HS1BP3 in model organisms like human cells and zebrafish has provided insights into its role in autophagy regulation and cancer-related processes, which may help in understanding the underlying mechanisms of these biological functions and diseases [1,2,4].

References:
1. Søreng, Kristiane, Knævelsrud, Helene, Holland, Petter, Simonsen, Anne. 2017. HS1BP3 inhibits autophagy by regulation of PLD1. In Autophagy, 13, 985-986. doi:10.1080/15548627.2017.1291483. https://pubmed.ncbi.nlm.nih.gov/28318354/
2. Hu, Xiaosi, Pan, Hongtao, Zhou, Shuai, Jin, Hao, Xu, Aman. 2022. HS1BP3, transcriptionally regulated by ESR1, promotes hepatocellular carcinoma progression. In Biochemical and biophysical research communications, 623, 111-119. doi:10.1016/j.bbrc.2022.07.047. https://pubmed.ncbi.nlm.nih.gov/35921704/
3. Yin, Zhangyuan, Klionsky, Daniel J. 2017. HS1BP3 provides a novel mechanism of negative autophagy regulation through membrane lipids. In Autophagy, 13, 779-780. doi:10.1080/15548627.2017.1305534. https://pubmed.ncbi.nlm.nih.gov/28323521/
4. Holland, Petter, Knævelsrud, Helene, Søreng, Kristiane, Di Paolo, Gilbert, Simonsen, Anne. 2016. HS1BP3 negatively regulates autophagy by modulation of phosphatidic acid levels. In Nature communications, 7, 13889. doi:10.1038/ncomms13889. https://pubmed.ncbi.nlm.nih.gov/28004827/
5. Takemoto, Y, Furuta, M, Sato, M, Kubo, M, Hashimoto, Y. . Isolation and characterization of a novel HS1 SH3 domain binding protein, HS1BP3. In International immunology, 11, 1957-64. doi:. https://pubmed.ncbi.nlm.nih.gov/10590261/
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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