TRPM7 Polyclonal Antibody, 20ul Live Cell Imaging where it partially colocalizes with

where it partially colocalizes with the nuclear lamina

and expression of this gene may be altered in tumors

Ubiquitin carboxyl-terminal hydrolase isozyme L1 encoded by UCHL1 belongs to the peptidase C12 family

Defects in this gene are the cause of non-syndromic mental retardation X-linked type 30 (MRX30)

somatic and familial gastrointestinal stromal tumors

TRPM7 Polyclonal Antibody, 20ul Live Cell Imaging where it partially colocalizes withThe protein encoded by this gene is both an ion channel and a serine threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. Defects in this gene are a cause of amyotrophic lateral sclerosis parkinsonism dementia complex of Guam. Alternative splicing of this gene results in multiple transcript variants.