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Strumpellin 抗体 (AA 380-530)

WASHC5 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7271349
发货至: 中国
  • 抗原 See all Strumpellin (WASHC5) 抗体
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    抗原表位
    • 3
    • 1
    • 1
    AA 380-530
    适用
    • 4
    • 4
    • 2
    宿主
    • 5
    克隆类型
    • 5
    多克隆
    标记
    • 5
    This Strumpellin antibody is un-conjugated
    应用范围
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    原理
    KIAA0196 Rabbit pAb
    交叉反应
    小鼠, 大鼠
    产品特性
    Polyclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 380-530 of human KIAA0196 (NP_055661.3).
    亚型
    IgG
  • 应用备注
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    别名
    KIAA0196 (WASHC5 产品)
    别名
    SPG8 antibody, AL022848 antibody, C76463 antibody, Kiaa0196 antibody, mKIAA0196 antibody, strumpellin antibody, WASH complex subunit 5 antibody, WASHC5 antibody, washc5 antibody, Washc5 antibody
    背景
    This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease, a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.,RTSC, SPG8, RTSC1, KIAA0196,KIAA0196
    基因ID
    9897
    UniProt
    Q12768
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