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SMC-462D-BI

NrCAM Antibody, Clone N364/51: Biotin

Cannot supply to this region.

SKU:
SMC-462D-BI
Additional Names:
Neuronal cell adhesion molecule, Bravo, hBravo, KIAA0343, MGC138845, MGC138846, Neuronal surface protein Bravo, Ng CAM related, Ng-CAM-related, NgCAM related cell adhesion molecule, NgCAM-related cell adhesion molecule, Nr CAM, Nr-CAM
Application:
WB, IF, ICC
Concentration:
1 mg/ml
Species Reactivity:
Mouse
Purification:
Protein G Purified
Storage Conditions:
See Manual
Supplier:
StressMarq Biosciences
Host:
Mouse
Reactivities:
Human, Mouse, Rat
Buffer:
136.36mM Ethanolamine, 133.23 mM Chlorides, 9.55mM Phosphates, 9.55mM Sodium Bicarbonate
Immunogen:
Fusion protein amino acids 30-845 (extracellular domain) of mouse NrCAM. Rat: 96% identity (795/822 amino acids identical). Human: 91% identity (753/822 amino acids identical) ~50% identity with Neurofascin.
Clone:
N364/51 (Formerly sold as S364-51)
Uniprot:
Q810U4
Synonyms:
B;Bravo;C030017F07Rik;C130076O07Rik;mBravo;mKIAA0343;neuron-glia-CAM-related cell adhesion molecule;neuronal cell adhesion molecule;neuronal surface protein Bravo;ng-CAM-related;ngCAM-related cell adhesion molecule;nr-CAM
Extra Details:
Neuronal Cell Adhesion Molecule (NrCAM) is a member of the immunoglobulin superfamily involved in axon guidance, synaptic stability, and neural circuit formation. It contains six Ig-like domains, five fibronectin type III repeats, and an intracellular domain that interacts with cytoskeletal and signaling proteins. NrCAM is expressed in the brain, spinal cord, and peripheral nervous system, where it mediates cell-cell interactions critical for axon pathfinding and synaptic targeting. It serves as a ligand for axonin-1 and F3/contactin, influencing growth cone motility and axon crossing at the midline. In neurodegenerative disease research, NrCAM has been linked to synaptic disassembly, neuroinflammation, and glioma progression. Its interaction with ankyrin-G and voltage-gated sodium channels at the node of Ranvier suggests a role in maintaining neuronal excitability and conduction. Dysregulation of NrCAM expression has been observed in Alzheimer's disease and high-grade gliomas, highlighting its dual role in neurodevelopment and pathology. NrCAM is also implicated in neuropsychiatric conditions such as autism and schizophrenia, making it a potential biomarker and therapeutic target for disorders involving synaptic dysfunction and neural connectivity.
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