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| Cat.No | ACP23641 | Target Name | PRPH |
|---|---|---|---|
| Target Synonyms | NEF 4; NEF4; Neurofilament 4 (57kD) ; Neurofilament 4; Perf; PERI_HUMAN; Peripherin; PRPH 1; prph; PRPH1 | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Expression Range | 1-470 |
| Protein Length | Full length protein | Purity | >85% (SDS-PAGE) |
| Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | P41219 |
|---|
Uniprot Id
P41219
Target Species
Human
Target Name
PRPH
Target Full Name
Peripherin
Target Function
Class-III neuronal intermediate filament protein. May form an independent structural network without the involvement of other neurofilaments or may cooperate with the neuronal intermediate filament proteins NEFL, NEFH, NEFM and INA to form a filamentous network. Assembly of the neuronal intermediate filaments may be regulated by RAB7A. Plays a role in the development of unmyelinated sensory neurons. May be involved in axon elongation and axon regeneration after injury. Inhibits neurite extension in type II spiral ganglion neurons in the cochlea.
Target Subcellular Location
Cytoplasm, cytoskeleton. Cell projection, axon. Perikaryon.
Target Protein Families
Intermediate filament family
Target Tissue Specificity
Expressed in the neurons of the outer hair cells in the organ of Corti and to a lesser extent in type I spiral ganglion cells.
Target Synonyms
NEF 4; NEF4; Neurofilament 4 (57kD) ; Neurofilament 4; Perf; PERI_HUMAN; Peripherin; PRPH 1; prph; PRPH1
Target Background
This gene encodes a cytoskeletal protein found in neurons of the peripheral nervous system. The encoded protein is a type III intermediate filament protein with homology to other cytoskeletal proteins such as desmin, and is a different protein that the peripherin found in photoreceptors. Mutations in this gene have been associated with susceptibility to amyotrophic lateral sclerosis.
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