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Huntington’s Disease Research Reagents

Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by CAG trinucleotide repeat expansion in the huntingtin (HTT) gene, producing toxic polyglutamine-expanded mutant huntingtin (mHTT). mHTT aggregation disrupts transcription, mitochondrial function, and synaptic signaling. HTT-lowering strategies (ASOs, siRNA, CRISPR) are in active clinical development, driving need for quantitative mHTT and biomarker assays.

Research Use Only (RUO)Not intended for diagnostic or therapeutic procedures.

Huntington’s Disease Research Reagents - key pathogenic pathways and research targets

Fig. 1 Key pathogenic pathways and research targets. abinScience product targets highlighted in orange.

abinScience provides validated antibodies, recombinant proteins, and ELISA kits for key Huntington’s disease research targets. All products are manufactured by our parent company AtaGenix Laboratories under ISO quality systems. Browse products below or contact us for custom antibody development.

Key Research Targets

Huntingtin (HTT/mHTT) — Polyglutamine-expanded mHTT aggregates into intranuclear inclusions and disrupts multiple cellular pathways. Anti-huntingtin antibodies (including polyQ-specific clones) enable mHTT quantification in CSF, aggregate detection by IHC, and HTT-lowering drug efficacy measurement.
→ Browse huntingtin antibodies & proteins

BDNF — Wild-type HTT promotes BDNF transcription and axonal transport; mHTT disrupts both, contributing to striatal neuron vulnerability. Anti-BDNF antibodies support neurotrophic signaling studies and neuroprotective therapy research.
→ Browse BDNF antibodies & proteins

NfL (Neurofilament Light Chain) — Plasma NfL is a validated biomarker correlating with HD disease stage and progression rate. Anti-NfL antibodies support longitudinal monitoring and clinical trial pharmacodynamic endpoints.

References

1. Tabrizi SJ, et al. Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities. Nat Rev Neurol. 2020;16(10):529-546. DOI

2. Byrne LM, et al. Neurofilament light protein in blood as a potential biomarker of neurodegeneration in Huntington’s disease. Neurology. 2017;89(22):2309-2317. DOI

3. Tabrizi SJ, et al. Targeting huntingtin expression in patients with Huntington’s disease. N Engl J Med. 2019;380(24):2307-2316. DOI

4. Bates GP, et al. Huntington disease. Nat Rev Dis Primers. 2015;1:15005. DOI

37 product results for "Huntington’s disease"

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