VMAT1 Polyclonal Antibody, 20ul Recombinant Protein Tay-Sachs disease and Marfan syndrome

Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes

and in vitro studies suggest that polyglutamine-expansion of ATXN1 may alter the repressor activity of this complex

With 50 reactions and 1 reaction per μl

It is thought to play a role in the tumorigenesis of colorectal cancers and the proliferative control of normal cells

This gene has been described as a marker for lung adenocarcinoma and renal cell carcinoma

VMAT1 Polyclonal Antibody, 20ul Recombinant Protein Tay-Sachs disease and Marfan syndromeThe vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993