Ret(Phospho Tyr1015) Polyclonal Antibody, 50ul Cell Screening and Imaging Defects in this gene have

Defects in this gene have been reported to be associated with protein alveolar proteinosis (PAP)

Mutations in this gene are associated with mental retardation

Nitric oxide synthase 1 is ubiquitously expressed

Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities

which is predominantly expressed in hemopoietic cells

Ret(Phospho Tyr1015) Polyclonal Antibody, 50ul Cell Screening and Imaging Defects in this gene haveThis gene, a member of the cadherin superfamily, encodes one of the receptor tyrosine kinases, which are cell surface molecules that transduce signals for cell growth and differentiation. This gene plays a crucial role in neural crest development, and it can undergo oncogenic activation in vivo and in vitro by cytogenetic rearrangement. Mutations in this gene are associated with the disorders multiple endocrine neoplasia, type IIA, multiple endocrine