Thermo Fisher Scientific HD Monoclonal Antibody (1D1)

Applications

Immunocytochemistry (ICC/IF)

• Tested Dilution: 10 µg/mL

ELISA

• Tested Dilution: 10 µg/mL

Product Specifications

Product Specific Information

Sequence of this protein is as follows:
CDGIMASGRK AVTHAIPALQ PIVHDLFVLR GTNKADAGKE LETQKEVVVS MLLRLIQYHQ VLEMFILVLQ QCHKENEDKW KRLSRQIADI ILPMLAKQQM HIDS

Target Information

Huntingtin is a disease gene linked to Huntington’s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product.

HD is a mid-life onset autosomal dominant neurodegenerative disease characterized by psychiatric disorders, dementia, and involuntary movements (chorea), leading to death in 10–20 years. The huntingtin locus spans 180 kb and consists of 67 exons.

The huntingtin gene is widely expressed and required for normal development. It exists as two alternatively polyadenylated forms with different abundance in fetal and adult tissues. The larger transcript (~13.7 kb) is predominantly expressed in brain, while the smaller (~10.3 kb) is more widely expressed.

The genetic defect leading to Huntington’s disease may not eliminate transcription but may alter mRNA or protein function.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.