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SPG7 抗体 (AA 115-141)

SPG7 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB23654 unconjugated
产品编号 ABIN656408
发货至: 中国
  • 抗原 See all SPG7 抗体
    SPG7 (Spastic Paraplegia 7 (SPG7))
    抗原表位
    • 7
    • 6
    • 6
    • 6
    • 6
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 115-141
    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
    • 14
    • 5
    • 4
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This SPG7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 115-141 amino acids from the Central region of human SPG7.
    克隆位点
    RB23654
    亚型
    Ig Fraction
    Top Product
    Discover our top product SPG7 Primary Antibody
  • 应用备注
    WB: 1:1000. IHC-P: 1:10~50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    储存方法
    SPG7 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    有效期
    6 months
  • 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 nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein 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. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq].
    分子量
    88235
    基因ID
    6687
    NCBI登录号
    NP_003110, NP_955399
    UniProt
    Q9UQ90
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