Product Name: Huntingtin, mutant-specific
Type: Mouse Monoclonal IgG1
Elisa:
WB: 1:500
Background: Huntingtons disease (HD) is a neurodegenerative disorder caused by an expanding polyglutamine repeat in the huntingtin (Htt) gene. HD is a mid-life onset autosomal dominant neurodegenerative disease that is characterized by psychiatric disorders, dementi
CAS NO.: 871700-17-3
Trametinib
Immunogen: Clone 1A771 was generated from Huntingtin mutant protein containing 62 glutamine amino acid repeats.
Buffer And Storage: Mouse monoclonal antibody purified with protein G chromatography is supplied in 100μl phosphate-buffered saline with 0.2% gelatin and 0.05% sodium azide. Store at 4°C, stable for 6 months. For long term storage, aliquot and store at -20°C.
Specificity: This antibody detects expanded polyQ repeat form of Htt in western blot, and does not detect normal Htt in a lymphoblast cell line from HD patients.
PubMed ID:http://aac.asm.org/content/50/12/4195.abstract