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Anti-AGER Polyclonal Antibody (HS925014)

Anti-AGER Polyclonal Antibody
Anti-AGER Polyclonal Antibody
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Overview
Catalog No.HS925014
Description
Anti-AGER Polyclonal Antibody (HS925014) is a rabbit polyclonal antibody detecting AGER in ELISA, IHC, WB. Suitable for Human.
Highlights
  • Affinity Purified — Minimal background and high purity for reliable results.
  • Multi-Application — Validated across multiple applications.
Species reactivityHuman
ApplicationsELISA, IHC, WB
Host speciesRabbit
IsotypeIgG
Clonality Polyclonal
Immunogen E. coli - derived recombinant Human AGER (Ile91-Asp274).
Target Receptor for advanced glycosylation end products, Advanced glycosylation end product-specific receptor, AGER, RAGE
Purification Purified by antigen affinity column.
Accession Q15109
Form Liquid
Storage buffer 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Product Usage Information
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

Advanced glycosylation end product-specific receptor (RAGE/AGER) is a ~42 kDa protein. Cell surface pattern recognition receptor that senses endogenous stress signals with a broad ligand repertoire including advanced glycation end products, S100 proteins, high-mobility group box 1 protein/HMGB1, amyloid beta/APP oligomers, nucleic acids, histones, phospholipids and glycosaminoglycans. Advanced glycosylation end products are nonenzymatically glycosylated proteins which accumulate in vascular tissue in aging and at an accelerated rate in diabetes. These ligands accumulate at inflammatory sites during the pathogenesis of various diseases including diabetes, vascular complications, neurodegenerative disorders and cancers, and RAGE transduces their binding into pro-inflammatory responses. Upon ligand binding, uses TIRAP and MYD88 as adapters to transduce the signal ultimately leading to the induction of inflammatory cytokines IL6, IL8 and TNFalpha through activation of NF-kappa-B. Interaction with S100A12 on endothelium, mononuclear phagocytes, and lymphocytes triggers cellular activation, with generation of key pro-inflammatory mediators.

1. Shang, D. et al. (2016) Scientific reports 6, 32180. PMID: 27572515
2. Evankovich, J. et al. (2017) FASEB journal : official publication of the Federation of American Societies for Experimental Biology 31, 3894-3903. PMID: 28515150
3. Wang, G. et al. (2021) Cell death discovery 7, 337. PMID: 34743181
4. Yang, Y. et al. (2022) Communications biology 5, 824. PMID: 35974093
5. Sirois, CM. et al. (2013) The Journal of experimental medicine 210, 2447-63. PMID: 24081950
6. Xue, J. et al. (2011) Structure (London, England : 1993) 19, 722-32. PMID: 21565706
7. Sakaguchi, M. et al. (2011) PloS one 6, e23132. PMID: 21829704
8. Yan, Z. et al. (2021) Nature communications 12, 308. PMID: 33436632
9. Moroz, OV. et al. (2009) BMC biochemistry 10, 11. PMID: 19386136
10. Fang, F. et al. (2010) FASEB journal : official publication of the Federation of American Societies for Experimental Biology 24, 1043-55. PMID: 19906677
Note For research use only.
Images
  • Anti-AGER Polyclonal Antibody

    Western blot

    Western blot analysis was performed using anti-AGER polyclonal antibody at 1ug/mL on recombinant AGER (Catalog No. HS925012).

References
Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
Enter any 2 of Mass, Concentration, Volume + Molecular Weight to solve for the unknown.
Mass
=
Concentration
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Volume
Molecular Weight *
g/mol
Formula
C₁ × V₁ = C₂ × V₂
Enter any 3 of the 4 values to solve for the unknown.
Stock Solution
C₁ (Stock Conc.)
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V₁ (Stock Vol.)
=
Working Solution
C₂ (Working Conc.)
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V₂ (Working Vol.)
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