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NUBPL 抗体 (AA 1-250)

This anti-NUBPL antibody is a 小鼠 单克隆 antibody detecting NUBPL in WB, FACS 和 IHC. Suitable for 人.
产品编号 ABIN2727688
发货至: 中国

Quick Overview for NUBPL 抗体 (AA 1-250) (ABIN2727688)

抗原

See all NUBPL 抗体
NUBPL (Nucleotide Binding Protein-Like (NUBPL))

适用

  • 39
  • 12
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2

宿主

  • 34
  • 5
小鼠

克隆类型

  • 36
  • 3
单克隆

标记

  • 16
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NUBPL antibody is un-conjugated

应用范围

  • 35
  • 17
  • 13
  • 13
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (IHC)

克隆位点

1C5
  • 抗原表位

    • 15
    • 8
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 1-250

    产品特性

    Homo sapiens nucleotide binding protein-like (NUBPL), transcript variant 1

    纯化方法

    Purified from mouse ascites fluids by affinity chromatography

    免疫原

    Human recombinant protein fragment corresponding to amino acids 1-250 of human NUBPL(NP_079428) produced in E.coli.

    亚型

    IgG1
  • 应用备注

    WB 1:500~2000, IHC 1:150, FLOW 1:100,

    说明

    The concentration of the product may vary between diferrent lots.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5-1.0 mg/mL

    缓冲液

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • 抗原

    NUBPL (Nucleotide Binding Protein-Like (NUBPL))

    别名

    NUBPL

    背景

    This gene encodes a member of the Mrp/NBP35 ATP-binding proteins family. The encoded protein is required for the assembly of the respiratory chain NADH dehydrogenase (complex I), an oligomeric enzymatic complex located in the inner mitochondrial membrane. The respiratory complex I consists of 45 subunits and 8 iron-sulfur (Fe/S) clusters. This protein is an Fe/S protein that plays a critical role in the assembly of respiratory complex I, likely by transferring Fe/S into the Fe/S-containing complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding distinct isoforms have been identified.

    分子量

    33.9 kDa

    基因ID

    80224

    NCBI登录号

    NM_025152

    HGNC

    80224
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