Tuberin(Phospho Thr1462) Polyclonal Antibody, 20ul Digital Burette Mutations in this gene cause

Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency

CDH2 encodes a classical cadherin and member of the cadherin superfamily

RCBTB1 (RCC1 and BTB domain containing protein 1) encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex

Peroxisomal biogenesis factor 11 beta encoded by PEX11B facilitates peroxisomal proliferation and interacts with PEX19

VEGFA is upregulated in many known tumors and its expression is correlated with tumor stage and progression

Tuberin(Phospho Thr1462) Polyclonal Antibody, 20ul Digital Burette Mutations in this gene causeMutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms.