MPZ 抗体
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北京 101111
Quick Overview for MPZ 抗体 (ABIN1513218)
抗原
See all MPZ 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Polyclonal Antibodies
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免疫原
- Recombinant protein of human MPZ
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亚型
- IgG
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anti-Myelin Protein Zero (MPZ) (AA 175-248) antibody
MPZ 适用: 大鼠, 小鼠, 犬 WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (C-Term) antibodyMPZ 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (AA 193-223), (C-Term) antibodyMPZ 适用: 人 WB, IHC (p), FACS, EIA 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (AA 1-258) antibodyMPZ 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (AA 186-215), (C-Term) antibodyMPZ 适用: 人 WB, IHC (p), FACS 宿主: 兔 Polyclonal RB21459 unconjugated
anti-Myelin Protein Zero (MPZ) antibodyMPZ 适用: 人 WB, IHC, FACS 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (AA 30-248) antibodyMPZ 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (AA 30-156) antibodyMPZ 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) antibodyMPZ 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myelin Protein Zero (MPZ) (Internal Region) antibodyVerified MPZ 适用: 大鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid freeze / thaw cycles
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- MPZ (Myelin Protein Zero (MPZ))
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别名
- MPZ
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背景
- This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism.,MPZ,CHM,CMT1,CMT1B,CMT2I,CMT2J,CMT4E,CMTDI3,CMTDID,DSS,HMSNIB,MPP,P0,Neuroscience,Cell Type Marker,Neurodegenerative Diseases,Neuron marker,Axon marker,MPZ
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分子量
- 27 kDa/34 kDa
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基因ID
- 4359
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UniProt
- P25189
抗原
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