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FGF23 抗体

FGF23 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5963411
发货至: 中国
  • 抗原 See all FGF23 抗体
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    适用
    • 58
    • 19
    • 14
    人, 小鼠
    宿主
    • 53
    • 23
    • 2
    克隆类型
    • 57
    • 21
    多克隆
    标记
    • 41
    • 11
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FGF23 antibody is un-conjugated
    应用范围
    • 42
    • 33
    • 17
    • 11
    • 9
    • 8
    • 6
    • 5
    • 4
    • 2
    • 1
    • 1
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    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human FGF23
    亚型
    IgG
    Top Product
    Discover our top product FGF23 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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. Avoid freeze / thaw cycles.
  • 抗原
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    别名
    FGF23 (FGF23 产品)
    别名
    FGF23 antibody, ADHR antibody, FGFN antibody, HPDR2 antibody, HYPF antibody, PHPTC antibody, fibroblast growth factor 23 antibody, fgf23 antibody, FGF23 antibody, Fgf23 antibody
    背景

    Synonyms: ADHR,FGF-23,Fgf23,FGF23,FGFN,Fibroblast growth factor 23,Fibroblast growth factor 23 C-terminal peptide,Fibroblast growth factor 23 precursor,HPDR2,HYPF,Phosphatonin,PHPTC,Tumor derived hypophosphatemia inducing factor,Tumor-derived hypophosphatemia-inducing factor

    Background: This gene encodes a member of the fibroblast growth factor family of proteins, which possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. The product of this gene regulates phosphate homeostasis and transport in the kidney. The full-length, functional protein may be deactivated via cleavage into N-terminal and C-terminal chains. Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR). Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC).

    分子量

    Observed_MW: 28kDa

    Calculated_MW: 27kDa

    基因ID
    8074
    UniProt
    Q9GZV9
    途径
    RTK signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Negative Regulation of Hormone Secretion
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