PDE3A Polyclonal Antibody, 100ul Organelle Studies With 1ml capacity and 1/100ml

With 1ml capacity and 1/100ml graduations

Cooperates with OLIG2 to establish the pMN domain of the embryonic neural tube

Loss of function mutations in SLC16A2 are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes

which is a characteristic motif of transcription factors

which transduce extracellular signals received by cell surface receptors into integrated cellular responses

PDE3A Polyclonal Antibody, 100ul Organelle Studies With 1ml capacity and 1/100mlThis gene encodes a member of the cGMP inhibited cyclic nucleotide phosphodiesterase (cGI PDE) family. cGI PDE enzymes hydrolyze both cAMP and cGMP, and play critical roles in many cellular processes by regulating the amplitude and duration of intracellular cyclic nucleotide signals. The encoded protein mediates platelet aggregation and also plays important roles in cardiovascular function by regulating vascular smooth muscle contraction and