CLCN3 anticorps (AA 293-752)

N° du produit ABIN7873455

L’anticorps anti-CLCN3 Polyclonal Lapin est utilisé pour la détection de CLCN3 dans des échantillons de Rat et Humain. Il a été validé pour WB, IHC, ICC, ELISA, IF et FACS.

Aperçu rapide pour CLCN3 anticorps (AA 293-752) (ABIN7873455)

Antigène: CLCN3 (Chloride Channel 3 (CLCN3))

Reactivité: Rat, Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLCN3 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunocytochemistry (ICC), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Détail du produit anti-CLCN3 anticorps

Épitope: AA 293-752

Fonction: CLCN3 Antibody / Chloride channel protein 3

Purification: Immunogen affinity purified

Immunogène: E.coli-derived human CLCN3 recombinant protein (Position: G293-R752) was used as the immunogen for the CLCN3 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the CLCN3 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the CLCN3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur CLCN3

Antigène: CLCN3 (Chloride Channel 3 (CLCN3))

Autre désignation: CLCN3

Sujet: CLCN3 antibody detects Chloride channel protein 3, encoded by the CLCN3 gene on chromosome 4q33. CLCN3 belongs to the CLC family of voltage-gated chloride channels and chloride/proton exchangers, which regulate membrane potential, cell volume, and ion homeostasis. CLCN3 is widely expressed across tissues but is most abundant in the nervous system, kidney, and muscle, where it supports vesicular acidification, endosomal trafficking, and chloride transport across membranes. It plays a vital role in maintaining neuronal excitability, synaptic transmission, and endolysosomal homeostasis.

Structurally, CLCN3 is a dimeric integral membrane protein with each subunit containing its own independent pore. It functions primarily as a Cl?/H+ antiporter rather than a pure chloride channel, coupling chloride efflux to proton influx. This electrogenic exchange contributes to acidification of endosomes and synaptic vesicles, processes essential for neurotransmitter storage and recycling. Mutations or dysregulation of CLCN3 impair endosomal acidification and lead to defective receptor trafficking, altered synaptic vesicle dynamics, and changes in neuronal function.

In the nervous system, CLCN3 contributes to synaptic vesicle function by facilitating neurotransmitter loading and release. Knockout mice lacking CLCN3 display severe neurodegeneration, retinal degeneration, and defects in hippocampal synaptic plasticity. These phenotypes underscore its importance in brain development and function. Additionally, CLCN3 supports cell volume regulation under osmotic stress, protecting neurons and glial cells from swelling-induced injury.

Pathologically, alterations in CLCN3 have been linked to epilepsy, intellectual disability, and neurodegenerative conditions. Some cancer studies have shown that CLCN3 expression is upregulated in gliomas and contributes to tumor growth and invasiveness by regulating intracellular chloride levels and endosomal signaling. As such, CLCN3 has been proposed as a potential therapeutic target in oncology and neurology. Researchers rely on CLCN3 antibody to study its role in these diverse processes, enabling insights into ion channel biology, synaptic function, and disease progression.

Experimentally, CLCN3 antibody has been applied in western blotting to detect the expected ~97 kDa band, in immunofluorescence microscopy to visualize endosomal and vesicular localization, and in immunohistochemistry to track expression in brain and kidney tissue. Co-immunoprecipitation studies using CLCN3 antibody have identified interacting partners including clathrin, synaptophysin, and vesicular proton ATPases, highlighting its integration in vesicular trafficking networks. Functional assays combining CLCN3 antibody with electrophysiological studies allow researchers to correlate protein abundance with transport activity. NSJ Bioreagents provides CLCN3 antibody to support neuroscience, physiology, and cancer research by ensuring reliable detection of this critical ion transporter.

UniProt: P51790