Periaxin anticorps (Intracellular, N-Term)
Aperçu rapide pour Periaxin anticorps (Intracellular, N-Term) (ABIN7885226)
Antigène
Voir toutes Periaxin (PRX) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Classe de qualité
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Épitope
- AA 155-170, Intracellular, N-Term
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Fonction
- A Rabbit Polyclonal Antibody to Periaxin
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Homologie
- Mouse,human - identical
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Purification
- Affinity purified on immobilized antigen.
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Immunogène
- (C)DVEFSFPKFSRLRR, corresponding to amino acid residues 155-170 of rat PRX
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Isotype
- IgG
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Indications d'application
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WB: 1:600
FC: The optimal concentration should be determined by the user
ICC: The optimal concentration should be determined by the user
IHC: 1:600
IP: The optimal concentration should be determined by the user
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Commentaires
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Negative Control: (ABIN7236245)
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- 0.2 mL double distilled water (DDW)
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Concentration
- 1 mg/mL
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Buffer
- PBS pH 7.4
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Agent conservateur
- Without preservative
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Stock
- -20 °C
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Stockage commentaire
- The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
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- Periaxin (PRX)
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Autre désignation
- PRX
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Sujet
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Synonyms: PRX, CMT4F
Description: Periaxin protein is a membrane-associated protein expressed in myelinating Schwann cells. It is required for the stable maintenance and development of a normal myelin sheath in the peripheral nervous system. It is also a member of cytoskeletal complexes in lens fibers where it plays an important role in maturation, packing, and membrane organization of lens fiber cell1,2. The periaxin gene (PRX) encodes two protein isoforms, L-periaxin and S-periaxin generated by alternative mRNA splicing. These proteins contain N-terminal PDZ domains (PSD-95/Discs-large/ZO-1) important for organizing protein-protein interactions.L-periaxin is a component of the dystroglycan-dystrophin-related protein-2 complex (DRP2) linking the Schwann cell cytoskeleton to the extracellular matrix. Its location changes during myelination, at first the protein is localized to the adaxonal plasma membrane and later, in the abaxonal plasma membrane. S-periaxin is distributed in a uniform manner in the cytoplasm and the nucleus of the Schwann cell1-3. Mutations in the Periaxin gene are known to cause autosomal recessive demyelinating in Type 4F Charcot-Marie-Tooth (CMT4F) and Dejerine-Sottas disease3.Periaxin knockout mice develop normally myelinated peripheral nervous system at first but develop a late onset demyelinating peripheral neuropathy1.
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ID gène
- 78960
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UniProt
- Q63425
Antigène
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