Human/Mouse FGF-23 Antibody Summary
Tyr25-Val251 (Arg179Gln)
Accession # Q9EPC2
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Mouse FGF-23 by Western Blot Effects of conditional deletion of Fgfr1 in Hyp osteocytes on gross appearance and bone-related gene expressions in 6-week-old mice.(A) Gross appearance, tail length, and body weight. Compared with control mice, Fgfr1Dmp1-cKO-null mice had normal gross appearance and body weight. However, Hyp mice showed considerably shorter tail length and lower body weight, compound Hyp;Fgfr1Dmp1-cKO-null mice displayed intermediate tail length and body weight between control and Hyp mice. Data are mean ± S.D. from 5–6 individual mice. (B and C) Western blot analysis of total Fgf2 and Fgf23 protein levels in bone. A representative Fgf2, Fgf23, and beta -Actin gel were shown in upper, middle, and lower panels of B, respectively. The intensity of bands was quantified using Image J software (https://rsb.info.nih.gov/ij/), and the data shown in C are mean ± S.D. from three independent experiments. Values sharing the same superscript in different groups are not significantly different at P<0.05. Image collected and cropped by CiteAb from the following publication (https://dx.plos.org/10.1371/journal.pone.0104154), licensed under a CC-BY license. Not internally tested by R&D Systems.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: FGF-23
FGF-23 is a secreted protein primarily expressed in the brain and thymus. Mutations in FGF-23 produced by osteomalacia tumors are linked to autosomal dominant hypophosphatemic rickets and several bone structure disorders.
Product Datasheets
Citations for Human/Mouse FGF-23 Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 6
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Twist1-Haploinsufficiency Selectively Enhances the Osteoskeletal Capacity of Mesoderm-Derived Parietal Bone Through Downregulation of Fgf23
Authors: N Quarto, S Shailendra, NP Meyer, S Menon, A Renda, MT Longaker
Front Physiol, 2018-10-15;9(0):1426.
Species: Mouse
Sample Types: Cell Lysates
Applications: Western Blot -
FGF23 is synthesised locally by renal tubules and activates injury-primed fibroblasts
Authors: ER Smith, SJ Tan, SG Holt, TD Hewitson
Sci Rep, 2017-06-13;7(1):3345.
Species: Mouse
Sample Types: Tissue Homogenates, Whole Tissue
Applications: IHC, Western Blot -
Osteocyte-specific deletion of Fgfr1 suppresses FGF23.
Authors: Xiao Z, Huang J, Cao L, Liang Y, Han X, Quarles L
PLoS ONE, 2014-08-04;9(8):e104154.
Species: Human
Sample Types: Cell Lysates
Applications: Western Blot -
Fibroblast growth factor 23 concentrations in healthy term infants during the early postpartum period.
Authors: Takaiwa M, Aya K, Miyai T
Bone, 2010-08-01;47(2):256-62.
Species: Human
Sample Types: Plasma
Applications: Western Blot -
Indoxyl sulfate induces left ventricular hypertrophy via the AhR-FGF23-FGFR4 signaling pathway
Authors: Kishimoto H, Nakano T, Torisu K et al.
Frontiers in cardiovascular medicine
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A computationally identified compound antagonizes excess FGF-23 signaling in renal tubules and a mouse model of hypophosphatemia
Authors: Zhousheng Xiao, Demian Riccardi, Hector A. Velazquez, Ai L. Chin, Charles R. Yates, Jesse D. Carrick et al.
Science Signaling
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