The protocadherins, a subgroup within the cadherin superfamily, are integral membrane proteins that mediate cell-cell adhesion in the nervous system, playing pivotal roles in neural development, circuit formation, and maintenance. PCDHA9 (Protocadherin Alpha 9) is a specific member of the α-protocadherin cluster, which is known to contribute to the molecular diversity of neural connections. PCDHA9, like other protocadherins, features extracellular cadherin repeats, which are crucial for mediating homophilic interactions, leading to cell-cell adhesion. These interactions are essential for proper neuronal patterning, synaptic specificity, and the establishment of neural networks. PCDHA9 participates in creating a complex molecular code that helps neurons to establish unique identities and connect appropriately with their target cells, ensuring the precise wiring of neural circuits.
Inhibitors of PCDHA9, therefore, are chemical entities that can disrupt the normal function of PCDHA9. These inhibitors might interact directly with the protein, hindering its ability to engage in homophilic interactions, or they might indirectly affect its function by interfering with associated signaling pathways or post-translational modifications. By disrupting the normal activity of PCDHA9, these inhibitors could potentially alter the pattern of neural connections, affecting the establishment and maintenance of neural circuits. Studying the effects of these inhibitors on PCDHA9 function can provide invaluable insights into the role of PCDHA9 in neural development and connectivity. It can help to unravel the complex molecular mechanisms underlying neural circuit formation and maintenance, contributing to our understanding of how the nervous system achieves its intricate and precise connectivity. Moreover, these inhibitors can serve as powerful tools in neuroscience research, enabling the dissection of PCDHA9's specific contributions to neural development and function.
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