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LONP1 抗体 (AA 148-334)

This 兔 多克隆 antibody specifically detects LONP1 in IHC (p). It exhibits reactivity toward 斑马鱼.
产品编号 ABIN7870769
发货至: 中国
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Quick Overview for LONP1 抗体 (AA 148-334) (ABIN7870769)

抗原

See all LONP1 抗体
LONP1 (Lon Peptidase 1, Mitochondrial (LONP1))

适用

  • 43
  • 28
  • 20
  • 1
斑马鱼

宿主

  • 42
  • 2

克隆类型

  • 42
  • 2
多克隆

标记

  • 15
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  • 1
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  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This LONP1 antibody is un-conjugated

应用范围

  • 32
  • 18
  • 13
  • 13
  • 7
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  • 5
  • 3
  • 3
  • 2
  • 2
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 15
    • 8
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 148-334

    原理

    Zebrafish Lonp1 Antibody / Lon protease homolog

    纯化方法

    Antigen affinity chromatography

    免疫原

    An E.coli-derived zebrafish Lonp1 recombinant protein (amino acids I148-A334) was used as the immunogen for the Zebrafish Lonp1 antibody.

    亚型

    Ig Fraction
  • 应用备注

    Optimal dilution of the Zebrafish Lonp1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the Zebrafish Lonp1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    LONP1 (Lon Peptidase 1, Mitochondrial (LONP1))

    别名

    Lonp1

    背景

    Lon protease homolog, mitochondrial is an enzyme that in humans is encoded by the LONP1 gene. It is mapped to 19p13.3. This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia.
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