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FGF23 抗体 (AA 48-251)

FGF23 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN4951022
发货至: 中国
  • 抗原 See all FGF23 抗体
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    抗原表位
    • 15
    • 5
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 48-251
    适用
    • 58
    • 19
    • 14
    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
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Antigen affinity
    免疫原
    Amino acids 48-251 of mouse FGF23 were used as the immunogen for the FGF23 antibody.
    亚型
    IgG
    Top Product
    Discover our top product FGF23 Primary Antibody
  • 应用备注
    Optimal dilution of the FGF23 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL
    限制
    仅限研究用
  • 缓冲液
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    储存条件
    -20 °C
    储存方法
    After reconstitution, the FGF23 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 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
    Fibroblast growth factor 23 is a protein that in humans is encoded by the FGF23 gene. 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).
    UniProt
    Q9EPC2
    途径
    RTK signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Negative Regulation of Hormone Secretion
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