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.
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.
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.
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
E. coli
Q13224
Tyr1133-Val1484
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
Human
ELISA, FACS, Functional assay
Human
IgG4, kappa
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
scFv-Fc
ZEB85
Human
ELISA
Mouse
IgG2a, kappa
C4
Human
ELISA, FCM
Mouse
IgG2a, kappa
SAA0477
PE
Human
ELISA, FCM
Mouse
IgG2a, lambda
SAA0471
PE
Human
ELISA, FCM
Mouse
IgG2a, kappa
SAA0477
PerCP
Human
ELISA, FCM
Mouse
IgG2a, lambda
SAA0471
PerCP
Human
ELISA, FCM
Mouse
IgG2a, kappa
SAA0477
APC
Human
ELISA, FCM
Mouse
IgG2a, lambda
SAA0471
APC