Why MingCelerWhy MingCeler

Why MingCeler

Why MingCeler

TurboMice™: Meet the Future of Mouse Model Creation

Making the UNTHINKABLE Real with TurboMice™

At Mingceler, we specialize in accelerating genetic research through our TurboMice™ technology, 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.



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TurboMice™ stands at the forefront ofnext-generation mouse model creation, providing unmatched efficiency andprecision in genetic engineering. By harnessing optimized tetraploid complementation technology, we offer researchers the ability to generate complex mouse models faster and more accurately than ever before. With theability to simultaneously edit multiple genes, TurboMice™ eliminates traditional bottlenecks like breeding and screening, dramatically reducing model development time. This revolutionary approachenables accelerated research and opens the door to more advanced and reliable scientific discoveries.

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ES bank

  • Efficiency & Speed
    Drastically reduces the time from gene targeting to mouse generation.
  • Versatility & Reproducibility
    A single validated ES cell clone can produce various mouse models (e.g., KO, KI, CKO,PM) reliably and repeatedly.
  • 3Rs benefit
    Born to Reduce & 100% Genotyping Efficiency.​
  • Archival Value & Safety
    Preserves precious genetic modifications indefinitely without the risks associated with live mouse colonies.

MingCeler Mouse Custome

  • TurboMice™ Knockout Mice
    Homozygous mice: 2~4 months
    3Rs benefit: no chimeras, no breeding selection required.
    Please Enter the number of Mice and Sex in the Requirements Section
  • TurboMice™ Knock in Mice
    • Targeted at a ‘Rosa26/H11’ locus
    • Reporter mice
    Any target site you wish to knock in
    Homozygous mice: 3~5 months
    3Rs benefit: no chimeras, no breeding selection required.
    Please Enter the number of Mice and Sex in the Requirements Section
  • TurboMice™ Humanized Mice
    • Humanizing point mutations
    • Humanizing domains, such as extracellular domains
    • Humanizing the entire gene
    • Humanizing multi-gene loci
    Unrivaled speed and convenience
    Homozygous mice: 3~5 months
    3Rs benefit: no chimeras, no breeding selection required
    Please Enter then umber of Mice and Sex in the Requirements Section
  • TurboMice™ Conditional knockout Mice
    Homozygous mice: 4~6 months(Cre+fl/fl)
    3Rs benefit: no chimeras, no breeding selection required
    Please Enter thenumber of Mice and Sex in the Requirements Section
  • TurboMice™ Point Mutant Mice
    Homozygous mice: 3~5 months
    3Rs benefit: no chimeras, no breeding selection required
    Please Enter thenumber of Mice and Sex in the Requirements Section
  • TurboMice™ Multi-Site Gene Editing Mice
    Homozygous mice: 4~6 months
    3Rs benefit: no chimeras, no breeding selection required
    Please Enter thenumber of Mice and Sex in the Requirements Section
  • TurboMice™ Transgenic Mice
    Homozygous mice: 3~5 months
    3Rs benefit: no chimeras, no breeding selection required
    Please Enter thenumber of Mice and Sex in the Requirements Section

Case Study

Highly cooperative chimeric super-SOX induces naive pluripotency across species Journal:Cell stem cell IF=19.8
Rapid generation of ACE2 humanized inbred mouse model for COVID-19 with tetraploid complementation Journal:National Science Review IF=16.3
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 Journal:Cell Research IF=25.9
SARS-CoV-2 envelope protein causes acute respiratory distress syndrome (ARDS)-like pathological damages and constitutes an antiviral target Journal:Cell Research IF=28.1
Captopril alleviates lung inflammation in SARS-CoV-2-infected hypertensive mice Journal:Zoological Research IF=4.7
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Online Quotation

We offer tailored gene editing solutions—get a free quote instantly.
Fill out the form, and we will contact you within two business days.
Alternatively, call us at 400-8388-113 or reach technical support at 18126776342 (also available on WeChat).