Periaxin 抗体 (Intracellular, N-Term)
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Quick Overview for Periaxin 抗体 (Intracellular, N-Term) (ABIN7885226)
抗原
See all Periaxin (PRX) 抗体适用
宿主
克隆类型
标记
应用范围
质量等级
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抗原表位
- AA 155-170, Intracellular, N-Term
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原理
- A Rabbit Polyclonal Antibody to Periaxin
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预测反应
- Mouse,human - identical
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纯化方法
- Affinity purified on immobilized antigen.
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免疫原
- (C)DVEFSFPKFSRLRR, corresponding to amino acid residues 155-170 of rat PRX
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亚型
- IgG
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应用备注
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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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说明
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Negative Control: (ABIN7236245)
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- 0.2 mL double distilled water (DDW)
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浓度
- 1 mg/mL
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缓冲液
- PBS pH 7.4
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储存液
- Without preservative
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储存条件
- -20 °C
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储存方法
- 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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别名
- PRX
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背景
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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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基因ID
- 78960
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UniProt
- Q63425
抗原
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