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FOXRED1 抗体 (AA 251-350) (Cy3)

This anti-FOXRED1 antibody is a 兔 多克隆 antibody detecting FOXRED1 in WB, IF (cc) 和 IF (p). Suitable for 小鼠 和 大鼠.
产品编号 ABIN1702926
发货至: 中国

Quick Overview for FOXRED1 抗体 (AA 251-350) (Cy3) (ABIN1702926)

抗原

See all FOXRED1 抗体
FOXRED1 (FAD-Dependent Oxidoreductase Domain Containing 1 (FOXRED1))

适用

  • 18
  • 17
  • 16
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
小鼠, 大鼠

宿主

  • 30
  • 2

克隆类型

  • 32
多克隆

标记

  • 14
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FOXRED1 antibody is conjugated to Cy3

应用范围

  • 32
  • 12
  • 12
  • 11
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 8
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 251-350

    交叉反应

    小鼠, 大鼠

    预测反应

    Human,Dog,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human FOXRED1

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    FOXRED1 (FAD-Dependent Oxidoreductase Domain Containing 1 (FOXRED1))

    别名

    FOXRED1

    背景

    Synonyms: FAD dependent oxidoreductase domain containing 1, FAD dependent oxidoreductase domain containing protein 1, FAD-dependent oxidoreductase domain-containing protein 1, FOXRED 1, FOXRED1, FP634, FXRD1_HUMAN, H17.

    Background: FOXRED1 is a 486 amino acid single-pass membrane protein. Utilizing FAD as a cofactor, FOXRED1 may act as a chaperone protein essential for the function of mitochondrial complex I. Mutations to FOXRED1 may result in mitochondrial complex I deficiency (MT-C1D), which results in a wide range of clinical maladies from lethal neonatal disease to adult onset neurodegenerative disorders. Common phenotypes of MT-C1D include cardiomyopathy, liver disease, Leigh syndrome, Leber hereditary optic neuropathy, and some forms of Parkinson disease. FOXRED1 exists as three alternatively spliced isoforms and is encoded by a gene mapping to human chromosome 11q24.2. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome.

    基因ID

    55572
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