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Cullin 7 抗体 (AbBy Fluor® 680)

This anti-Cullin 7 antibody is a 兔 多克隆 antibody detecting Cullin 7 in WB 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN5000720
发货至: 中国
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北京 101111
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Beijing Economic Technological Development Area
Room 801-803
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Quick Overview for Cullin 7 抗体 (AbBy Fluor® 680) (ABIN5000720)

抗原

See all Cullin 7 (CUL7) 抗体
Cullin 7 (CUL7)

适用

  • 42
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  • 1
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  • 1
人, 小鼠, 大鼠

宿主

  • 41
  • 1

克隆类型

  • 41
  • 1
多克隆

标记

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  • 2
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  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
  • 1
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This Cullin 7 antibody is conjugated to AbBy Fluor® 680

应用范围

  • 28
  • 12
  • 9
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human Cullin 7

    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

    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

    Cullin 7 (CUL7)

    别名

    Cullin 7

    背景

    Synonyms: CUL-7, CUL7, CUL7_HUMAN, Cullin-7, dJ20C7.5, KIAA0076.

    Background: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.

    基因ID

    9820

    途径

    ER-Nucleus Signaling
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