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FBXW4 抗体 (Cy5)

FBXW4 适用: 人, 小鼠, 大鼠 IF (p) 宿主: 兔 Polyclonal Cy5
产品编号 ABIN1416678
发货至: 中国
  • 抗原 See all FBXW4 抗体
    FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
    适用
    • 38
    • 22
    • 20
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    人, 小鼠, 大鼠
    宿主
    • 39
    • 2
    克隆类型
    • 41
    多克隆
    标记
    • 16
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FBXW4 antibody is conjugated to Cy5
    应用范围
    • 23
    • 21
    • 11
    • 8
    • 3
    • 3
    • 3
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human SHFM3
    亚型
    IgG
    Top Product
    Discover our top product FBXW4 Primary Antibody
  • 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 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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
    4 °C
    储存方法
    Store at 4°C
    有效期
    12 months
  • 抗原
    FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
    别名
    SHFM3 (FBXW4 产品)
    背景

    Probably recognizes and binds to some phosphorylated proteins and promotes their ubiquitination and degradation. Likely to be involved in key signaling pathways crucial for normal limb development. May participate in Wnt signaling.Involvement in disease:Defects in FBXW4 are a cause of split-hand/foot malformation type 3 (SHFM3) . SHFM3 is an autosomal dominant disorder characterized by hypoplasia/aplasia of the central digits with fusion of the remaining digits.

    Synonyms: DAC, Dactylin, F box and WD 40 domain containing protein 4, F box and WD 40 domain protein 4, F box and WD repeat domain containing 4, F box/WD repeat containing protein 4, F box/WD repeat protein 4, F-box and WD-40 domain-containing protein 4, F-box/WD repeat-containing protein 4, FBW 4, FBW4, FBWD 4, FBWD4, FBXW 4, FBXW4, FBXW4_HUMAN, SHFM 3, SHSF 3, SHSF3, Split hand/foot malformation ectrodactyly type.

    基因ID
    6468
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