TS1R1 Polyclonal Antibody, 50ul Micro Centrifuge Tubes Mutations in this gene are

Mutations in this gene are potential candidates for causing neurosensory deafness

This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm

Defects in PPT1 are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1

Rac interactive binding) domain

which play a role in cytoskeletal formation by regulating actin polymerization

TS1R1 Polyclonal Antibody, 50ul Micro Centrifuge Tubes Mutations in this gene areThe protein encoded by this gene is a G protein coupled receptor and is a component of the heterodimeric amino acid taste receptor T1R1+3. The T1R1+3 receptor responds to L amino acids but not to D enantiomers or other compounds. Most amino acids that are perceived as sweet activate T1R1+3, and this activation is strictly dependent on an intact T1R1+3 heterodimer. Multiple transcript variants encoding different isoforms have been found for this gene.