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- Table of Contents
and ELISA kits, proteins related to Glial cells.
Glial cells, often overshadowed by neurons, are the unsung heroes of the nervous system. These versatile cells provide essential support, protection, and nourishment to neurons, ensuring seamless communication and overall brain health. Beyond their foundational roles, glial cells are pivotal in maintaining homeostasis, forming myelin sheaths, and responding to injury and disease within the nervous system. Recent research has unveiled their significant involvement in various neurological disorders, making them a critical focus for therapeutic advancements. Our specialized antibodies targeting glial cell markers enhance the precision and effectiveness of these studies, enabling scientists to unravel the complexities of glial functions and their impact on human health. Explore our cutting-edge antibody solutions to propel your glial cell research to new heights and contribute to groundbreaking neurological breakthroughs.
PA1050
M00144-1
M00979-1
| Protein Name | Gene Name | Function |
|---|---|---|
| GFAP | GFAP | Intermediate filament protein in astrocytes |
| S100B | S100B | Calcium-binding protein involved in astrocyte signaling |
| IBA1 | AIF1 | Microglial activation and phagocytosis |
| OLIG2 | OLIG2 | Transcription factor critical for oligodendrocyte differentiation |
| MBP | MBP | Myelin basic protein essential for myelin sheath formation |
| PLP1 | PLP1 | Proteolipid protein important for myelin stability |
| CD11b | ITGAM | Integrin alpha M involved in microglial adhesion and migration |
| AQP4 | AQP4 | Water channel protein in astrocyte end-feet regulating water homeostasis |
| SOX10 | SOX10 | Transcription factor involved in oligodendrocyte development |
| CNPase | CNP | Enzyme involved in myelin sheath maintenance |
| MOG | MOG | Myelin oligodendrocyte glycoprotein involved in myelin structure |
| CD68 | CD68 | Lysosomal marker in activated microglia |
| GLT-1 | SLC1A2 | Glutamate transporter regulating excitatory neurotransmission |
| TREM2 | TREM2 | Receptor involved in microglial phagocytosis and survival |
| P2RY12 | P2RY12 | Purinergic receptor involved in microglial chemotaxis |
| MAG | MAG | Myelin-associated glycoprotein important for myelin-axon interaction |
| FABP7 | FABP7 | Fatty acid binding protein involved in astrocyte lipid metabolism |
| ALDH1L1 | ALDH1L1 | Aldehyde dehydrogenase involved in astrocyte differentiation |
| Vimentin | VIM | Intermediate filament protein involved in astrocyte structure |
| Nestin | NES | Intermediate filament protein in neural progenitor cells and astrocytes |
Astrocytes, the most abundant glial cells in the central nervous system, play a pivotal role in maintaining neuronal function and overall brain health. One of the key sub-research areas within glial cell studies focuses on astrocyte-neuron interactions. Astrocytes regulate the extracellular environment by controlling ion concentrations, particularly potassium, and by removing excess neurotransmitters from synaptic clefts. This regulation is essential for proper synaptic transmission and preventing neuronal excitotoxicity, which can lead to cell damage or death. Additionally, astrocytes contribute to the formation and maintenance of the blood-brain barrier, ensuring selective permeability and protecting the neural tissue from harmful substances. They also release gliotransmitters, such as glutamate and ATP, which modulate synaptic activity and plasticity, thereby influencing learning and memory processes. Understanding the intricate communication between astrocytes and neurons is crucial for unraveling the complexities of various neurological disorders, including epilepsy, Alzheimer's disease, and amyotrophic lateral sclerosis (ALS). Ongoing research in this area aims to elucidate the molecular mechanisms governing these interactions, offering potential therapeutic targets for mitigating neurodegenerative diseases and enhancing neural repair strategies.
Microglia, the resident immune cells of the central nervous system, are essential for maintaining homeostasis, defending against pathogens, and facilitating tissue repair. A significant sub-research area within glial cell studies is the investigation of microglial activation and its role in neuroinflammation. Under resting conditions, microglia continuously survey the neural environment for signs of injury or infection. Upon activation, they undergo morphological and functional changes, releasing pro-inflammatory cytokines, chemokines, and reactive oxygen species to combat perceived threats. While acute microglial activation is protective, chronic or excessive activation can lead to sustained neuroinflammation, contributing to the pathogenesis of various neurodegenerative diseases such as Parkinson's disease, multiple sclerosis, and chronic traumatic encephalopathy (CTE). Researchers are particularly interested in understanding the signaling pathways and molecular triggers that regulate microglial responses, as well as identifying factors that can modulate their activity to prevent or reduce harmful inflammation. Advances in this field hold promise for developing targeted therapies that can either suppress detrimental microglial activation or enhance their neuroprotective functions, thereby offering new avenues for treating a range of neurological disorders.