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Recombinant Peripherin antibody (full length)

The Mouse Monoclonal anti-Peripherin antibody (Clone rPJM50) (ABIN8093403) specifically detects Peripherin in WB and IHC. The antibody is reactive with Human samples.
Catalog No. ABIN8093403
$640.46
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Recombinant Peripherin antibody (full length) (ABIN8093403)

Target

See all Peripherin (PRPH) Antibodies
Peripherin (PRPH)

Antibody Type

Recombinant Antibody

Reactivity

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Human

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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This Peripherin antibody is un-conjugated

Application

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  • 1
Western Blotting (WB), Immunohistochemistry (IHC)

Grade

Carrier-free

Clone

RPJM50
  • Binding Specificity

    • 5
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    • 1
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    full length

    Purpose

    PRPH Antibody / Peripherin (azide and preservative free)

    Immunogen

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

    Isotype

    IgG2b, kappa
  • Application Notes

    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
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    -20 °C,-80 °C

    Storage Comment

    PRPH/Peripherin antibody with sodium azide - store at 2 to 8oC, antibody without sodium azide - store at -20 to -80oC.
  • Target

    Peripherin (PRPH)

    Alternative Name

    PRPH

    Background

    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
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