电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

MPZ 抗体

MPZ 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1513218
发货至: 中国
  • 抗原 See all MPZ 抗体
    MPZ (Myelin Protein Zero (MPZ))
    适用
    • 40
    • 27
    • 26
    • 15
    宿主
    • 50
    • 4
    • 3
    • 1
    克隆类型
    • 54
    • 4
    多克隆
    标记
    • 24
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This MPZ antibody is un-conjugated
    应用范围
    • 46
    • 28
    • 13
    • 13
    • 13
    • 8
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB)
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Polyclonal Antibodies
    免疫原
    Recombinant protein of human MPZ
    亚型
    IgG
    Top Product
    Discover our top product MPZ Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Avoid freeze / thaw cycles
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    MPZ (Myelin Protein Zero (MPZ))
    别名
    MPZ (MPZ 产品)
    别名
    CHM antibody, CMT1 antibody, CMT1B antibody, CMT2I antibody, CMT2J antibody, CMT4E antibody, CMTDI3 antibody, CMTDID antibody, DSS antibody, HMSNIB antibody, MPP antibody, P0 antibody, Mpp antibody, P-zero antibody, p0 antibody, sc:d0186 antibody, wu:fc04b11 antibody, wu:fi30g06 antibody, zgc:103775 antibody, myelin protein zero antibody, myelin protein zero S homeolog antibody, MPZ antibody, Mpz antibody, mpz antibody, mpz.S antibody
    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
    分子量
    27 kDa/34 kDa
    基因ID
    4359
    UniProt
    P25189
You are here:
客服