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SPG7 抗体 (AA 71-120)

This anti-SPG7 antibody is a 兔 多克隆 antibody detecting SPG7 in WB 和 ELISA. Suitable for 人.
产品编号 ABIN7231494
发货至: 中国

Quick Overview for SPG7 抗体 (AA 71-120) (ABIN7231494)

抗原

See all SPG7 抗体
SPG7 (Spastic Paraplegia 7 (SPG7))

适用

  • 27
  • 5
  • 3
  • 3
  • 1
  • 1

宿主

  • 19
  • 11

克隆类型

  • 21
  • 9
多克隆

标记

  • 25
  • 1
  • 1
  • 1
  • 1
  • 1
This SPG7 antibody is un-conjugated

应用范围

  • 28
  • 11
  • 10
  • 5
  • 5
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • 抗原表位

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 71-120

    原理

    SPG7 Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of SPG7 protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human SPG7 protein at AA range: 71-120

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    SPG7 (Spastic Paraplegia 7 (SPG7))

    别名

    SPG7

    背景

    Rabbit Anti-SPG7 Polyclonal Antibody,Paraplegin, Cell matrix adhesion regulator, Spastic paraplegia 7 protein,SPG7 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 SPG7 cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.,SPG7

    分子量

    observerd band 87kDa

    基因ID

    6687

    UniProt

    Q9UQ90
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