PTPRH Rabbit Polyclonal Antibody, 100ul Protein Modification Mutations in this particular gene

Mutations in this particular gene cause synpolydactyly

It catalyzes the phosphorylation of glycerol by ATP

moderately in lung

Defects in ATG16L1 are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10)

TBX18 codes for a member of an evolutionarily conserved family of transcription factors that plays a crucial role in embryonic development

PTPRH Rabbit Polyclonal Antibody, 100ul Protein Modification Mutations in this particular geneThe protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth differentiation mitotic cycle and oncogenic transformation. This PTP possesses an extracellular region a single transmembrane region and a single intracytoplasmic catalytic domain and thus represents a receptor type PTP. The extracellular region