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RFESD 抗体 (AA 51-157) (AbBy Fluor® 594)

This anti-RFESD antibody is a 兔 多克隆 antibody detecting RFESD in WB, IF (cc) 和 IF (p). Suitable for 大鼠.
产品编号 ABIN2805917
发货至: 中国

Quick Overview for RFESD 抗体 (AA 51-157) (AbBy Fluor® 594) (ABIN2805917)

抗原

RFESD (Rieske (Fe-S) Domain Containing (RFESD))

适用

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大鼠

宿主

  • 32
  • 1

克隆类型

  • 32
  • 1
多克隆

标记

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This RFESD antibody is conjugated to AbBy Fluor® 594

应用范围

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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 5
    • 2
    • 2
    • 1
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    • 1
    AA 51-157

    交叉反应

    大鼠

    预测反应

    Human,Mouse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human RFESD

    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

    RFESD (Rieske (Fe-S) Domain Containing (RFESD))

    别名

    RFESD

    背景

    Synonyms: Rieske Fe S domain containing, Rieske domain containing protein, RFESD_HUMAN.

    Background: RFESD, also known as Rieske domain-containing protein, is a 157 amino acid protein that binds one 2Fe-2S cluster per subunit. Involved in metal ion binding, RFESD contains one Rieske domain. The RFESD gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 5q15. Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

    基因ID

    317671
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