Y13142H Recombinant Human Fibronectin Freezers cardiac defects and autonomic dysfunction

cardiac defects and autonomic dysfunction

The TC-treated surface improves surface wettability and promotes efficient cell attachment

Mutations in this gene are associated with Crohn's disease and inflammatory bowel disease

This product was previously listed under catalog number 15-18850 and is now updated to BF-79357129 for improved product management

The gene mutation results in primary NAA deficiency (hypoacetylaspartia)

Y13142H Recombinant Human Fibronectin Freezers cardiac defects and autonomic dysfunctionDescription Fibronectin, also known as FN, is a high molecular weight glycoprotein widely found in the extracellular matrix. Its molecular structure contains multiple binding domains that enable selective interactions with various macromolecules such as fibrin, heparin, bacteria, and cell surface receptors. Through these interactions, it participates in numerous physiological processes. Fibronectin plays important roles in mediating cell matrix and