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WDR35 抗体 (N-Term)

This anti-WDR35 antibody (ABIN1449959) is a Rabbit Polyclonal antibody detecting WDR35 in IHC (p), EIA. Suitable for Human.
产品编号 ABIN1449959
发货至: 中国

Quick Overview for WDR35 抗体 (N-Term) (ABIN1449959)

抗原

See all WDR35 抗体
WDR35 (WD Repeat Domain 35 (WDR35))

适用

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宿主

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克隆类型

  • 9
多克隆

标记

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This WDR35 antibody is un-conjugated

应用范围

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Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
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    N-Term

    纯化方法

    Affinity chromatography purified via peptide column

    免疫原

    16 amino acid synthetic peptide near the amino terminus of Human WDR35

    亚型

    IgG
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 浓度

    1.0 mg/mL

    缓冲液

    PBS containing 0.02 % Sodium Azide as preservative

    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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原

    WDR35 (WD Repeat Domain 35 (WDR35))

    别名

    WDR35

    背景

    WD40 repeats are a common structural module in eukaryotic proteins, and proteins containing WD40 domains have a wide range of functions, including signal transduction, cell cycle regulation, RNA splicing, and transcription. One such protein, WDR35, also known as CED2, has been shown to be mutated in patients with Sensenbrenner syndrome/cranioectodermal dysplasia (CED), an autosomal-recessive disease that is characterized by craniosynstosis and ectodermal and skeletal abnormalities. WDR35 localizes to cilia and dentrosomes during embryogenesis and human and mouse fibroblasts that lack this gene fail to produce cilia. Mutations in this gene can also cause short-rib polydactyly syndromes due to abnormal ciliogenesis.Synonyms: IFT121, Intraflagellar transport protein 121 homolog, KIAA1336, WD repeat-containing protein 35

    基因ID

    57539

    NCBI登录号

    NP_001006658

    途径

    Hedgehog Signaling
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