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SPG7 抗体 (AA 1-250)

SPG7 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6148342
发货至: 中国
  • 抗原 See all SPG7 抗体
    SPG7 (Spastic Paraplegia 7 (SPG7))
    抗原表位
    • 7
    • 7
    • 6
    • 6
    • 6
    • 4
    • 1
    • 1
    • 1
    • 1
    AA 1-250
    适用
    • 29
    • 4
    • 3
    • 1
    • 1
    宿主
    • 21
    • 8
    克隆类型
    • 23
    • 6
    多克隆
    标记
    • 19
    • 2
    • 2
    • 2
    • 2
    • 2
    This SPG7 antibody is un-conjugated
    应用范围
    • 28
    • 14
    • 13
    • 5
    • 4
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    序列
    MAVLLLLLRA LRRGPGPGPR PLWGPGPAWS PGFPARPGRG RPYMASRPPG DLAEAGGRAL QSLQLRLLTP TFEGINGLLL KQHLVQNPVR LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE RLRTLLVIAV VMSLLNALST SGGSISWNDF VHEMLAKGEV QRVQVVPESD VVEVYLHPGA VVFGRPRLAL MYRMQVANID KFEEKLRAAE DELNIEAKDR IPVSYKRTGF
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Polyclonal Antibodies
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-250 of human SPG7 (NP_003110.1).
    亚型
    IgG
    Top Product
    Discover our top product SPG7 Primary Antibody
  • 应用备注
    WB,1:1000 - 1:2000,IHC,1:50 - 1:200
    说明

    HIGH QUALITY

    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
    SPG7 (Spastic Paraplegia 7 (SPG7))
    别名
    SPG7 (SPG7 产品)
    别名
    CAR antibody, CMAR antibody, PGN antibody, SPG5C antibody, AI452278 antibody, AU015315 antibody, Cmar antibody, SPG7, paraplegin matrix AAA peptidase subunit antibody, SPG7 antibody, Spg7 antibody
    背景
    This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.,SPG7,CAR,CMAR,PGN,SPG5C,Cell Biology & Developmental Biology,Ubiquitin,Neuroscience,Neurodegenerative Diseases,SPG7
    分子量
    53 kDa/88 kDa
    基因ID
    6687
    UniProt
    Q9UQ90
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