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AB172473

Anti-RAGE antibody [EPR12206]

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(7 Publications)

Rabbit Recombinant Monoclonal RAGE antibody. Suitable for WB and reacts with Mouse, Rat samples. Cited in 7 publications.

View Alternative Names

RAGE, AGER, Advanced glycosylation end product-specific receptor, Receptor for advanced glycosylation end products

1 Images
Western blot - Anti-RAGE antibody [EPR12206] (AB172473)
  • WB

Lab

Western blot - Anti-RAGE antibody [EPR12206] (AB172473)

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

Exposure time :

Lane 1 to 6 : 3 second
Lane 7 to 11 : 20 seconds

The expression profile and molecular mass observed is consistent with what has been described in the literature (PMID : 16315007; 18355449; 18245812)

All lanes:

Western blot - Anti-RAGE antibody [EPR12206] (ab172473) at 1/1000 dilution

Lane 1:

Mouse lung lysates at 20 µg

Lane 2:

Mouse brain lysates at 20 µg

Lane 3:

Mouse kidney lysates at 20 µg

Lane 4:

Mouse heart lysates at 20 µg

Lane 5:

Mouse liver lysates at 20 µg

Lane 6:

Mouse spleen lysates at 20 µg

Lane 7:

Rat lung lysates at 20 µg

Lane 8:

Rat brain lysates at 20 µg

Lane 9:

Rat kidney lysates at 20 µg

Lane 10:

Rat heart lysates at 20 µg

Lane 11:

Rat spleen lysates at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Predicted band size: 42 kDa

Observed band size: 43 kDa

false

  • Carrier free

    Anti-RAGE antibody [EPR12206] - BSA and Azide free

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR12206

Isotype

IgG

Carrier free

No

Reacts with

Mouse, Rat

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Specificity

Recent tests in our laboratory showed that the antibody detects the band of interest in tissue lysates, but it did not detect the protein in cell lysate.

RAGE is typically expressed at low levels under normal physiological conditions in majority of tissues except normal lung tissue. When testing other tissues, please use lung tissue as a positive control.

Reactivity data

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Product details

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Preservative: 0.01% Sodium azide Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

RAGE also known as Receptor for Advanced Glycation End-products is a multi-ligand cell surface receptor with a molecular weight of approximately 45 kDa. It belongs to the immunoglobulin superfamily consisting of three extracellular immunoglobulin-like domains a transmembrane domain and a cytoplasmic tail. RAGE is widely expressed in various tissues throughout the body with high expression levels in the lungs heart and cells of the nervous system. The receptor can interact with several ligands such as advanced glycation end-products (AGEs) amyloid beta and S100/calgranulin proteins facilitating signal transduction into the cells.
Biological function summary

RAGE functions in the immune and inflammatory response where it mediates cell signaling that leads to cellular activation and the release of pro-inflammatory cytokines. It acts as part of complexes with different proteins contributing to cellular processes such as proliferation and migration. RAGE also plays roles in the regulation of oxidative stress and apoptosis impacting cellular health and survival. Researchers employ tools like 'anti-RAGE' antibodies and 'RAGER ELISA' assays to measure and study RAGE expression levels and its interactions in various experimental setups.

Pathways

RAGE is significantly involved in the NF-kB pathway and the MAPK signaling cascade. Its activation can lead to the release of NF-kB a transcription factor that plays an essential role in immune and inflammatory responses. RAGE interacts with proteins such as p38 MAPK leading to a cascade of events that regulate inflammation and stress responses. The signaling pathways involving RAGE are important in maintaining cell homeostasis and responding to cellular stressors and tools like 'anti-RAGE' and 'mouse RAGE' antibodies serve to elucidate these complex pathways further.

RAGE has strong associations with chronic diseases like diabetes and Alzheimer's disease. In diabetes RAGE binds to AGEs contributing to inflammation and vascular complications where it often interacts with proteins like iNOS and VEGF. In Alzheimer's disease RAGE is implicated in the accumulation and toxicity of amyloid-beta peptides interacting with proteins such as APP and tau. Understanding RAGE's role in these diseases can aid in developing therapeutic strategies employing reagents such as 'phen RAGE' and 'anti-RAGE' for targeted treatment approaches.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

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, phospholipids and glycosaminoglycans (PubMed : 27572515, PubMed : 28515150, PubMed : 34743181). Advanced glycosylation end products are nonenzymatically glycosylated proteins which accumulate in vascular tissue in aging and at an accelerated rate in diabetes (PubMed : 21565706). 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 or inflammatory cytokines IL6, IL8 and TNFalpha through activation of NF-kappa-B (PubMed : 21829704, PubMed : 33436632). Interaction with S100A12 on endothelium, mononuclear phagocytes, and lymphocytes triggers cellular activation, with generation of key pro-inflammatory mediators (PubMed : 19386136). Interaction with S100B after myocardial infarction may play a role in myocyte apoptosis by activating ERK1/2 and p53/TP53 signaling (By similarity). Contributes to the translocation of amyloid-beta peptide (ABPP) across the cell membrane from the extracellular to the intracellular space in cortical neurons (PubMed : 19906677). ABPP-initiated RAGE signaling, especially stimulation of p38 mitogen-activated protein kinase (MAPK), has the capacity to drive a transport system delivering ABPP as a complex with RAGE to the intraneuronal space. Participates in endothelial albumin transcytosis together with HMGB1 through the RAGE/SRC/Caveolin-1 pathway, leading to endothelial hyperpermeability (PubMed : 27572515). Mediates the loading of HMGB1 in extracellular vesicles (EVs) that shuttle HMGB1 to hepatocytes by transferrin-mediated endocytosis and subsequently promote hepatocyte pyroptosis by activating the NLRP3 inflammasome (PubMed : 34743181). Promotes also extracellular hypomethylated DNA (CpG DNA) uptake by cells via the endosomal route to activate inflammatory responses (PubMed : 24081950, PubMed : 28515150).
See full target information AGER

Publications (7)

Recent publications for all applications. Explore the full list and refine your search

Heliyon 6:e05672 PubMed33313438

2020

HMGB1 as a potential biomarker and therapeutic target for severe COVID-19.

Applications

Unspecified application

Species

Unspecified reactive species

Ruochan Chen,Yan Huang,Jun Quan,Jiao Liu,Haichao Wang,Timothy R Billiar,Michael T Lotze,Herbert J Zeh,Rui Kang,Daolin Tang

Scientific reports 9:19150 PubMed31844158

2019

Targeting AXL and RAGE to prevent geminin overexpression-induced triple-negative breast cancer metastasis.

Applications

Unspecified application

Species

Unspecified reactive species

Daniel Ryan,Jim Koziol,Wael M ElShamy

Journal of inflammation research 12:25-33 PubMed30774410

2019

Myelin basic protein charge isomers change macrophage polarization.

Applications

Unspecified application

Species

Unspecified reactive species

Elene Tsitsilashvili,Maia Sepashvili,Marika Chikviladze,Lali Shanshiashvili,David Mikeladze

Clinical and experimental pharmacology & physiology 44:760-770 PubMed28394420

2017

Tiron ameliorates high glucose-induced cardiac myocyte apoptosis by PKCδ-dependent inhibition of osteopontin.

Applications

Unspecified application

Species

Unspecified reactive species

Ping Jiang,Deling Zhang,Hong Qiu,Xianqi Yi,Yemin Zhang,Yingkang Cao,Bo Zhao,Zhongyuan Xia,Changhua Wang

Molecular medicine reports 14:5217-5222 PubMed27840921

2016

Recombinant human soluble thrombomodulin protects against brain injury in a CVST rat model, via downregulation of the HMGB1-RAGE axis.

Applications

Unspecified application

Species

Unspecified reactive species

Jian-Jun Gu,Jie-Bin Chen,Jian-He Zhang,Hao Zhang,Shou-Sen Wang

Oncotarget 7:20869-89 PubMed26989079

2016

Geminin overexpression-dependent recruitment and crosstalk with mesenchymal stem cells enhance aggressiveness in triple negative breast cancers.

Applications

Unspecified application

Species

Unspecified reactive species

Suryatheja Ananthula,Abhilasha Sinha,Mohamed El Gassim,Simran Batth,Gailen D Marshall,Lauren H Gardner,Yoshiko Shimizu,Wael M ElShamy

Experimental and therapeutic medicine 10:584-590 PubMed26622358

2015

Small interfering RNA targeting receptor for advanced glycation end products suppresses the generation of proinflammatory cytokines.

Applications

Unspecified application

Species

Unspecified reactive species

Xiao-Wei Wang,Wei-Dong Li,Jin-Rong Xia,Zhan Li,Xiao-Gang Cai
View all publications

Product promise

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