Smad1(Phospho Ser465) Polyclonal Antibody, 100ul High Speed Micro-Centrifuges Mutations in this gene are

Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria

They act as adapters for transmitting various signals in response to stimuli through cytokine and growth factor receptors

PTM:Phosphorylation of Thr-148 by MAPK8 in response to different stress conditions such as

6-linked sialic acid

Smad1(Phospho Ser465) Polyclonal Antibody, 100ul High Speed Micro-Centrifuges Mutations in this gene areThe protein encoded by this gene belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein mediates the signals of the bone morphogenetic proteins (BMPs), which are involved in a range of biological activities including cell