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Ships within 48 hours · Estimated delivery Jul 20 - Jul 25
For Your Every Summer RSVP, with Code: SUMMER15
Description
RAGE Recombinant Rabbit mAb (S-1846-41)Product Specification Host Rabbit Antigen RAGE Synonyms Advanced glycosylation end product specific receptor; Receptor for advanced glycosylation end products; AGER Immunogen Recombinant Protein Location Secreted, Cell membrane Accession Q15109 Clone Number S 1846 41 Antibody Type Recombinant mAb Isotype IgG Application WB Reactivity Ms, Rt Positive Sample mouse lung, rat lung Predicted Reactivity Bv Purification Protein A Concentration 0. 5 mg ml
Product Specification
| Host | Rabbit |
| Antigen | RAGE |
| Synonyms | Advanced glycosylation end product-specific receptor; Receptor for advanced glycosylation end products; AGER |
| Immunogen | Recombinant Protein |
| Location | Secreted, Cell membrane |
| Accession | Q15109 |
| Clone Number | S-1846-41 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB |
| Reactivity | Ms, Rt |
| Positive Sample | mouse lung, rat lung |
| Predicted Reactivity | Bv |
| Purification | Protein A |
| Concentration | 0.5 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000 | Ms, Rt |
Background
The RAGE (Receptor for Advanced Glycation End-products) protein is a multiligand receptor belonging to the immunoglobulin superfamily, widely expressed in various cell types such as endothelial cells, smooth muscle cells, neurons, and immune cells. Its primary function involves binding to multiple ligands, including AGEs, HMGB1, and S100 proteins, to regulate processes such as inflammation, oxidative stress, cell migration, proliferation, and apoptosis. Under physiological conditions, RAGE expression is relatively low; however, it is significantly upregulated in pathological states such as chronic inflammation, diabetes, atherosclerosis, neurodegenerative diseases, and cancer. Activation of RAGE typically occurs through signaling pathways like NF-κB and MAPK, promoting the expression of inflammatory factors and oxidative stress-related molecules, thereby exacerbating tissue damage and disease progression. As a result, RAGE is considered a critical molecular target in various chronic diseases, and research into its inhibitors holds potential therapeutic value.
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