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Signal Transduction Growth Factors/Hormones FGF

Human FGF23 ELISA Kit (ab267652)

Price and availability

452 304 ₸

Availability

Order now and get it on Thursday February 25, 2021

Human FGF23 ELISA Kit (ab267652)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Sensitivity: 0.3 ng/ml
  • Range: 0.307 ng/ml - 75 ng/ml
  • Sample type: Cell culture media, Plasma, Serum
  • Detection method: Colorimetric
  • Assay type: Sandwich (quantitative)
  • Reacts with: Human

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Overview

  • Product name

    Human FGF23 ELISA Kit
    See all FGF 23 kits
  • Detection method

    Colorimetric
  • Precision

    Intra-assay
    Sample n Mean SD CV%
    Overall
    Inter-assay
    Sample n Mean SD CV%
    Overall
  • Sample type

    Serum, Plasma, Cell culture media
  • Assay type

    Sandwich (quantitative)
  • Sensitivity

    0.3 ng/ml
  • Range

    0.307 ng/ml - 75 ng/ml
  • Recovery

    Sample specific recovery
    Sample type Average % Range
    Serum 135 122% - 145%
    Plasma 144 138% - 147%
    Cell culture media 143 133% - 149%
  • Assay duration

    Multiple steps standard assay
  • Species reactivity

    Reacts with: Human
  • Product overview

    Human FGF23 ELISA Kit is designed for the quantitative determination of FGF23 in cell culture supernatants, plasma and serum samples.


    ΔNote: Human FGF-23 concentration is low in normal serum/plasma, and may not be detectable in this assay.


    This assay employs an antibody specific for human FGF23 coated on a 96-well plate. Standards and samples are pipetted into the wells and FGF23 present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-human FGF23 antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of FGF23 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

  • Platform

    Microplate

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 1 x 96 tests
    20X Wash Buffer 1 x 25ml
    350X HRP-Streptavidin Concentrate 1 x 200µl
    5X Assay Diluent B 1 x 15ml
    Anti-Human FGF23 coated Microplate (12 x 8 wells) 1 unit
    Assay Diluent C 1 x 30ml
    Biotinylated Anti-Human FGF23 Detection Antibody 2 vials
    Human FGF23 Standard (Lyophilized) 2 vials
    Stop Solution 1 x 8ml
    TMB Substrate Solution 1 x 12ml
  • Research areas

    • Signal Transduction
    • Growth Factors/Hormones
    • FGF
    • Signal Transduction
    • Cytoskeleton / ECM
    • Extracellular Matrix
    • Structures
    • Bone
    • Stem Cells
    • Lineage Markers
    • Endoderm
    • Cancer
    • Growth factors
    • FGF
    • Developmental Biology
    • Lineage specification
    • Endoderm
  • Function

    Regulator of phosphate homeostasis. Inhibits renal tubular phosphate transport by reducing SLC34A1 levels. Upregulates EGR1 expression in the presence of KL (By similarity). Acts directly on the parathyroid to decrease PTH secretion (By similarity). Regulator of vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization.
  • Tissue specificity

    Expressed in osteogenic cells particularly during phases of active bone remodeling. In adult trabecular bone, expressed in osteocytes and flattened bone-lining cells (inactive osteoblasts).
  • Involvement in disease

    Defects in FGF23 are the cause of autosomal dominant hypophosphataemic rickets (ADHR) [MIM:193100]. ADHR is characterized by low serum phosphorus concentrations, rickets, osteomalacia, leg deformities, short stature, bone pain and dental abscesses.
    Defects in FGF23 are a cause of hyperphosphatemic familial tumoral calcinosis (HFTC) [MIM:211900]. HFTC is a severe autosomal recessive metabolic disorder that manifests with hyperphosphatemia and massive calcium deposits in the skin and subcutaneous tissues.
  • Sequence similarities

    Belongs to the heparin-binding growth factors family.
  • Post-translational
    modifications

    Following secretion this protein is inactivated by cleavage into a N-terminal fragment and a C-terminal fragment. The processing is effected by proprotein convertases.
    O-glycosylated by GALT3. Glycosylation is necessary for secretion; it blocks processing by proprotein convertases when the O-glycan is alpha 2,6-sialylated. Competition between proprotein convertase cleavage and block of cleavage by O-glycosylation determines the level of secreted active FGF23.
  • Cellular localization

    Secreted. Secretion is dependent on O-glycosylation.
  • Target information above from: UniProt accession Q9GZV9 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Alternative names

    • ADHR
    • FGF-23
    • Fgf23
    • FGF23_HUMAN
    • 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
    see all
  • Database links

    • Entrez Gene: 8074 Human
    • Omim: 605380 Human
    • SwissProt: Q9GZV9 Human
    • Unigene: 287370 Human

    Images

    • Standard curve
      Standard curve

      Human FGF23 ELISA kit (ab267652) Standard curve.

      Data provided for demonstration purposes only. A new standard curve must be generated for each assay performed.

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
    For licensing inquiries, please contact partnerships@abcam.com

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