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WDR35 抗体 (N-Term)

WDR35 适用: 人 IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1449959
发货至: 中国
  • 抗原 See all WDR35 抗体
    WDR35 (WD Repeat Domain 35 (WDR35))
    抗原表位
    • 4
    • 3
    • 1
    • 1
    • 1
    N-Term
    适用
    • 9
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 9
    克隆类型
    • 9
    多克隆
    标记
    • 6
    • 1
    • 1
    • 1
    This WDR35 antibody is un-conjugated
    应用范围
    • 4
    • 4
    • 1
    • 1
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    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
    Top Product
    Discover our top product WDR35 Primary Antibody
  • 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 (WDR35 产品)
    别名
    4930459M12Rik antibody, 4931430C06 antibody, mKIAA1336 antibody, RGD1564116 antibody, Wdr35 antibody, CED2 antibody, IFT121 antibody, im:7159945 antibody, si:ch211-206k20.4 antibody, WD repeat domain 35 antibody, Wdr35 antibody, WDR35 antibody, wdr35 antibody
    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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