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Recombinant Rat Hmgb1, Fc-tagged

Cat.No.: Hmgb1-293R
Product Overview: The extracellular domain of rat HMGB1 (aa 24-215) is fused to the N-terminus of the Fc region of human IgG1.
Description: HMGB1 was originally discovered as an essential DNA-binding protein for regulating p53, NF-κB and other important proteins. It is secreted from activated dentric cells, macrophage and nectrotic cells, and acts as a ligand for RAGE, TLR-2 and TLR-4 expressed on surrounding cells. As a result, HMGB1 activates Rac, CDC42 and NF-κB inducing localized innate immunity of damaged tissue, tissue regeneration by recruitment of stem cells and hemostasis by induction of tissue factor expression. HMGB1 is also causative agent of various diseases as it causes localized inflammation such as arteriosclerosis, chronic rheumatoid arthritis and nephritis.
Source: CHO Cells
Species: Rat
Tag: Fc
Form: Lyophilized from 0.2μm-filtered solution in PBS.
Purity: ≥98% (SDS-PAGE)
Stability: Stable for at least 1 year after receipt when stored at -20°C. Working aliquots are stable for up to 3 months when stored at -20°C.
Storage: Short Term Storage: +4°C; Long Term Storage: -20°C. Avoid freeze/thaw cycles.
Gene Name: Hmgb1 high mobility group box 1 [ Rattus norvegicus ]
Official Symbol: Hmgb1
Synonyms: HMGB1; high mobility group box 1; high mobility group protein B1; HMG-1; amphoterin; high mobility group 1; heparin-binding protein p30; high mobility group protein 1; Hmg1; Ac2-008; MGC93598; MGC93599;
Gene ID: 25459
mRNA Refseq: NM_012963
Protein Refseq: NP_037095
Pathway: Androgen Receptor Signaling Pathway, organism-specific biosystem; Base excision repair, organism-specific biosystem; Base excision repair, conserved biosystem;
Function: 5S rRNA binding; DNA binding, bending; DNA binding, bending; RAGE receptor binding; RAGE receptor binding; bent DNA binding; calcium-dependent protein kinase regulator activity; crossed form four-way junction DNA binding; cytokine activity; cytokine activity; double-stranded DNA binding; four-way junction DNA binding; glycolipid binding; heparin binding; heparin binding; open form four-way junction DNA binding; peptide binding; protein binding; protein dimerization activity; protein kinase activator activity; repressing transcription factor binding; sequence-specific DNA binding transcription factor activity; single-stranded DNA binding; transcription factor binding; transcription factor binding;

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