Recombinant Peripherin anticorps (full length)

N° du produit ABIN8093402

L’anticorps anti-Peripherin Monoclonal Souris est utilisé pour la détection de Peripherin dans des échantillons de Humain. Il a été validé pour WB et IHC.

Aperçu rapide pour Recombinant Peripherin anticorps (full length) (ABIN8093402)

Antigène: Peripherin (PRPH)

Type d'anticorp: Recombinant Antibody

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Peripherin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Clone: RPJM50

Détail du produit anti-Peripherin anticorps

Épitope: full length

Fonction: PRPH Antibody / Peripherin

Immunogène: Prokaryotic recombinant protein corresponding to the full-length peripherin molecule was used as the immunogen for the PRPH/Peripherin antibody.

Isotype: IgG2b, kappa

Information d'application

Indications d'application: 1. Optimal dilution of the PRPH/Peripherin antibody should be determined by the researcher.

2. This PRPH/Peripherin antibody is recombinantly produced by expression in CHO cells.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.05 % BSA, 0.05 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C,-80 °C

Stockage commentaire: PRPH/Peripherin antibody with sodium azide - store at 2 to 8oC, antibody without sodium azide - store at -20 to -80oC.

Détails sur Peripherin

Antigène: Peripherin (PRPH)

Autre désignation: PRPH

Sujet: PRPH antibody, also known as Peripherin antibody, recognizes Peripherin, a type III intermediate filament protein encoded by the PRPH gene and primarily expressed in neurons of the peripheral nervous system. Peripherin is localized to the cytoplasm, where it assembles into intermediate filament networks that support neuronal structure and axonal integrity. PRPH expression is enriched in peripheral sensory and autonomic neurons and is also detected in certain central nervous system neurons during development and regeneration. As a neuronal cytoskeletal protein, Peripherin plays a critical role in maintaining axonal architecture and structural stability.

PRPH antibody detects a protein composed of a conserved alpha-helical rod domain flanked by non-helical head and tail domains, characteristic of intermediate filament family members. Peripherin can form homopolymers or heteropolymers with other neuronal intermediate filament proteins, including neurofilament light chain, contributing to regulation of axonal caliber and cytoskeletal organization. Expression of Peripherin is developmentally regulated and is often upregulated following neuronal injury, linking PRPH to nerve regeneration and repair processes.

Functionally, Peripherin is involved in neurite outgrowth, axonal elongation, and cytoskeletal remodeling. It is widely used as a marker of peripheral nerve fibers in research applications and is particularly associated with small diameter sensory neurons. Altered PRPH expression or abnormal accumulation of Peripherin has been reported in neurodegenerative conditions, including models of amyotrophic lateral sclerosis, where cytoskeletal dysregulation may contribute to motor neuron pathology. These findings highlight the importance of Peripherin in neuronal maintenance and disease-associated structural changes.

The PRPH gene is located on chromosome 12 and is transcriptionally regulated during neuronal differentiation and stress responses. Because of its selective neuronal expression pattern and involvement in cytoskeletal dynamics, detection of PRPH protein provides insight into peripheral nerve biology, neuronal development, and regeneration mechanisms.

This recombinant monoclonal PRPH antibody (clone rPJM50) targets Peripherin protein in research applications. PRPH antibody supports investigation of neuronal cytoskeletal organization, axonal growth, injury response, and neurodegenerative disease models.

UniProt: P41219