ZN496 Polyclonal Antibody, 20ul Mechanical Pipette Mutations in MTR have been

Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G

Defects in protein kinase C gamma have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14)

This cyclin has been shown to specifically interact with CIP/KIP family of CDK inhibitors

In the presence of nucleoside triphosphates and the small GTP binding protein Ran

ZN496 Polyclonal Antibody, 20ul Mechanical Pipette Mutations in MTR have beenMay be involved in transcriptional regulation.,Belongs to the krueppel C2H2 type zinc finger protein family.,Contains 1 KRAB domain.,Contains 1 SCAN box domain.,Contains 5 C2H2 type zinc fingers.,