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  • Custom TurboMice™

Categories

  • 分子生物学
    •    - PCR/qPCR/RT-qPCR
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    •    - 基因合成
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    •    - 多肽合成
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    •    - 细胞转染
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    •    - 细胞增殖
    •    - 细胞结构
  • 生物化学
    •    - 蛋白检测
    •    - 蛋白表达
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    •    - 免疫分析
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Custom TurboMice™

Custom TurboMice™

TurboMice™ is next-generation mouse model generation technology developed by MingCeler company, which harnesses optimized tetraploid complementation to deliver fully homozygous mouse models in just 2–4 months—60% faster than traditional breeding methods. Unlike conventional approaches that require 6–12 months of tedious breeding cycles, our process starts with precision editing of embryonic stem cells (ESCs) for targeted gene knockouts, floxing, or multi-locus modifications. We then use tetraploid complementation to develop these ESCs directly into experiment-ready mice, skipping the need for chimeric F1 and F2 generations. This method ensures 100% genotype certainty from the F0 generation, eliminating the guesswork of heterozygous screening and saving researchers thousands of hours spent on colony management.
 


Key Features

• The world's first platform to industrialize Tetraploid Complementation Technology, enabling one-step generation of homozygous models (directly addresses the chimerism pain point associated with traditional methods).

• Outstanding performance in complex models, enable one-step acquisition of CKO/CKI Homozygotes (e.g., mutti-gene editing, humanzied genomic replacement).

• Customized Genetic Models with Guaranteed Homozygosity—No Breeding Required.

• Delivery cycle: only 2-4 months (over 60% faster than traditional methods).
 

Service Options

Service Type Features Lead Time
Custom KO Mice • Homozygous mice
• No chimeras, no breeding selection required
2~4 months
Custom KI Mice • Any target site you wish to knock in
• Homozygous mice
• No chimeras, no breeding selection required
3~5 months
Custom CKO Mice • Homozygous mice
• No chimeras, no breeding selection required
3~5 months
Custom Humanized Mice • Humanizing point mutations
• Humanizing the entire gene
• Humanizing multi-gene loci
• Homozygous mice
• No chimeras, no breeding selection required
3-5 months
Custom Point Mutant Mice • Homozygous mice
• No chimeras, no breeding selection required
3~5 months
Custom Transgenic Mice • Homozygous mice
• No chimeras, no breeding selection required
3~5 months
Custom Muti-site Gene Editing Mice • Homozygous mice
• No chimeras, no breeding selection required
4~6 months


sirna synthesisQuote Guide

To inquire about this service, please choose one of the options below:
1. Fill out Enquiry Form to submit your request.
2. Download the Quote Form and send to sales@lifesct.com.
3. Register and log in to your account to submit your request via Service Quote system.
 

Case Study

Traditional transgenic K18-ACE2 mice are generated through random exogenous insertion, which precludes precise editing and results in a model lacking tissue specificity. In contrast, TurboMice™ humanized ACE2 models allow for organ-specific expression (Figures C and D), more accurately mimicking clinical disease manifestations.

By optimizing enhancers, we successfully upgraded our humanized ACE2 mouse model four times in just one year. Humanized ACE2 expression has increased steadily with each iteration and now nears endogenous levels—a feat that would take traditional methods significantly longer and cost much more to achieve.
 

Publications

1. Highly cooperative chimeric super-SOX induces naive pluripotency across species. 
Publication: Cell stem cell 

2. Dalbavancin binds ACE2 to block its interaction with SARS-CoV-2 spike protein and is effective in inhibiting SARS-CoV-2 infection in animal models. 
Publication: Cell Research

3. SARS-CoV-2 envelope protein causes acute respiratory distress syndrome (ARDS)-like pathological damages and constitutes an antiviral target. 
Publication: Cell Research

 

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