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CCDC39 抗体 (FITC)

This anti-CCDC39 antibody is a Rabbit Polyclonal antibody detecting CCDC39 in WB. Suitable for Human, Mouse, Rat.
产品编号 ABIN887704
发货至: 中国

Quick Overview for CCDC39 抗体 (FITC) (ABIN887704)

抗原

See all CCDC39 抗体
CCDC39 (Coiled-Coil Domain Containing 39 (CCDC39))

适用

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人, 小鼠, 大鼠

宿主

  • 26

克隆类型

  • 26
多克隆

标记

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This CCDC39 antibody is conjugated to FITC

应用范围

  • 25
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Western Blotting (WB)
  • 交叉反应

    预测反应

    Mouse,Rat,Cow,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CCDC39

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 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

    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

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    CCDC39 (Coiled-Coil Domain Containing 39 (CCDC39))

    别名

    Ccdc39

    背景

    Synonyms: CCD39_HUMAN, Ccdc39, Coiled-coil domain-containing protein 39.

    Background: Required for assembly of dynein regulatory complex (DRC) and inner dynein arm complexes, which are responsible for ciliary beat regulation, thereby playing a central role in motility in cilia and flagella. Not required for outer dynein arm complexes assembly.Tissue specificity:Mainly expressed in nasal brushings and, to a lesser extent, in lungs and testis.Involvement in disease:Defects in CCDC39 are the cause of primary ciliary dyskinesia type 14 (CILD14) . A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia, reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.

    基因ID

    339829
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