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Western blot analysis with Rabbit Anti-CASPR2 Monoclonal Antibody, Clone FF19 (STMA00227) showing detection of Human CASPR2 protein in a transient over-expression (OE) lysate (OriGene LY402278). Block: 2% skim milk + 2% BSA for 1 hour at RT. Primary Antibody: Rabbit Anti-Human CASPR2 Recombinant Monoclonal [FF19] (STMA00227) at 1:1000 for 2 hours at RT. Secondary Antibody: Goat anti-rabbit IgG-HRP (H&L) at 1:5000 for 1 hour at RT.
Key Features

Anti-CASPR2 Antibody [FF19]

SKU STMA00227
Antibody Type Recombinant Monoclonal
Applications WB
Applications IHC
Applications ICC/IF
Reactivity Human
Reactivity Mouse
Reactivity Rat
Host Species Rabbit
Isotype IgG Kappa
$854

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Description

CASPR2 Antibody [FF19]

CASPR2 Antibody [FF19] is a rabbit recombinant monoclonal antibody directed against CASPR2, offered by Assay Genie for research applications. Reported applications include WB, IHC and ICC/IF. Reported reactivity: Human, Mouse and Rat. Supplied as IgG Kappa, purified by MabSelect™ PrismA.

CASPR2, a member of the neurexin superfamily, is a critical axonal membrane protein that regulates the organization of myelinated nerve fibers. Unlike CASPR, which localizes to the paranodal junction, CASPR2 is enriched at the juxtaparanodal region of the axon, where it functions as a membrane scaffold essential for clustering voltage-gated Kv1 potassium channels. This spatial arrangement is vital for maintaining axonal excitability and signal fidelity. CASPR2 interacts with contactin-2 and cytoskeletal adaptor protein 4.1B to stabilize the juxtaparanodal domain, contributing to the compartmentalization of axonal regions around the nodes of Ranvier. Disruption of CASPR2 function impairs ion channel localization and axonal conduction, leading to altered neuronal signaling. Emerging evidence links CASPR2 dysfunction to a spectrum of neurodevelopmental and neurodegenerative disorders, including epilepsy, autism spectrum disorders, and autoimmune encephalitis. In neurodegenerative disease contexts, CASPR2-associated disorganization of axonal domains may contribute to demyelination, synaptic dysfunction, and progressive neuronal loss. Given its role in maintaining axonal architecture and electrical signaling, CASPR2 is increasingly recognized as a potential biomarker and therapeutic target in diseases affecting white matter integrity and neural connectivity. This antibody is also available conjugated to ATTO 390, ATTO 488, ATTO 594, APC, Biotin, FITC, HRP, PerCP and RPE. Supplied in 100 µg. For research use only; not for diagnostic or therapeutic procedures.

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