TM2D1 Polyclonal Antibody, 20ul Protein Post-translational Modification RCBTB1 maps to a region

RCBTB1 maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies

A chromosomal aberration involving CRTC1 is found in mucoepidermoid carcinomas

This gene contains trinucleotide (CTG) repeat length polymorphism in the coding region

Mutations in this gene result in Diamond-Blackfan anemia

TM2D1 Polyclonal Antibody, 20ul Protein Post-translational Modification RCBTB1 maps to a regionThe protein encoded by this gene is a beta amyloid peptide binding protein. It contains a structural module related to that of the seven transmembrane domain G protein coupled receptor superfamily and known to be important in heterotrimeric G protein activation. Beta amyloid peptide has been established to be a causative factor in neuron death and the consequent diminution of cognitive abilities observed in Alzheimer's disease. This protein may be a