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HPRT Locus Targeting

Since 1998, ingenious targeting laboratory has completed over 2,500 custom gene targeting projects, with hundreds utilizing safe harbor locus integration to achieve stable and predictable transgene expression. The HPRT locus represents one of the most versatile genomic sites for insertion of exogenous DNA, enabling researchers to generate consistent models without the variability associated with random integration approaches.

HPRT locus targeting allows researchers to insert reporter genes, selection markers, or therapeutic transgenes at a well-characterized genomic location that supports robust expression across diverse tissue types. This approach is particularly valuable when studying genes where single-copy integration and consistent expression levels are essential for research outcomes.

2,500+
Projects Completed
800+
Publications
26+
Years Experience
100%
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Our scientific consultants are ready to discuss your research requirements and recommend the optimal approach for your program. Initial consultation is provided at no charge.

✦ New for 2026

Breeding Scheme Architect

Plan complex multi-allele breeding strategies, calculate expected genotype ratios, and estimate time to experimental cohorts—all before starting your project.

Visualize multi-generation breeding paths
Calculate Mendelian ratios automatically
Estimate timeline to study ready cohorts

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Allele 1Gene-flox (conditional)
Allele 2Cre-driver (tissue-specific)
TargetHomozygous knockout

→ 3 generations to target genotype

Frequently asked questions

HPRT locus targeting successfully accommodates large genomic fragments, including BAC inserts spanning 100+ kilobases. Pre germline ES cell characterization confirms insertion structure regardless of insert size, ensuring researchers receive predictable models.

Heterozygous females carry one copy of the targeted HPRT allele and one wild-type allele on their second X chromosome. X inactivation results in approximately 50% of cells expressing the transgene, creating a mosaic tissue distribution. Hemizygous males express the transgene uniformly across all tissues.

HPRT locus expression generally yields intermediate levels suitable for most reporter and transgenic applications. Specific expression depends on the transgene promoter driving expression, the surrounding chromatin context, and the specific insert design. ES cell characterization does not predict transgene expression levels, so researchers should plan founder line screening.

Yes, HPRT safe harbor locus targeting is fully compatible with LoxP site insertion enabling Cre mediated excision. This combination creates conditional transgenic models where exogenous gene expression can be induced or eliminated in tissue specific or temporally controlled contexts.

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