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Anti hmgb1 ab18256

Manufactured by Abcam
Sourced in United Kingdom

Anti-HMGB1 (ab18256) is a primary antibody that specifically binds to the High Mobility Group Box 1 (HMGB1) protein. HMGB1 is a nuclear protein involved in DNA binding and transcriptional regulation. This antibody can be used to detect and study the HMGB1 protein in various research applications.

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4 protocols using anti hmgb1 ab18256

1

Quantifying Autophagy Pathway Activation

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Chloroquine (C6628) was obtained from Sigma-Aldrich. Oxaliplatin (OXA, S1224), and quinacrine (S5435) were purchased from Selleckchem. Torin 1 (2273-5) was ordered from BioVision. Anti-ATF4 (CST 11815S), anti-CHOP antibody (2895), anti-eIF2α antibody (9722), anti-p-eIF2α (Ser51) (9721S), anti-Histone H3 (9715S), anti-ATG5 antibody (12994), and anti-PERK (5683) antibodies were obtained from Cell Signaling Technology (CST). An anti-LC3 antibody (NB100-2220) was obtained from Novus Biologicals. An anti-GAPDH antibody (GTX100118) was ordered from GeneTex. Anti-TFE3 antibody (HPA023881), and anti-Flag (F3165) antibody were ordered from Sigma-Aldrich. Anti-TFEB antibody (303-673A) was ordered from Bethyl Laboratories. Anti-HMGB1 (ab18256), and anti-Calreticulin (ab92516) antibodies were ordered from Abcam. Goat anti-rabbit (111-035-003), and goat anti-mouse (115-035-003) secondary antibodies were products of Jackson ImmunoResearch. Alexa Fluor 594 goat anti-rabbit IgG (A-11012), Alexa Fluor 488 goat anti-rabbit IgG (A-11034), and Alexa Fluor 488 (A-11008) goat anti-rabbit secondary antibodies were ordered from Invitrogen.
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2

RAGE-Fc Fusion Protein Modulation

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Purified human soluble RAGE-Fc fusion protein (sRAGE) was purchased from Y-biologics (Daejeon, Republic of Korea). Ang II, losartan, caffeic acid phenethyl ester (CAPE), and fluorescein isothiocyanate (FITC)-labeled dextran 40 were obtained from Sigma-Aldrich (St. Louis, MO, USA). Purified anti-HMGB1 antibody (651402) was purchased from BioLegend (San Diego, CA, USA). Anti-AT1R antibody (AAR-011) was purchased from Alomone Labs (Hadassah Ein Kerem, Israel). Anti-RAGE (ab3611), anti-mDia1 (ab129167), and anti-HMGB1 (ab18256) antibodies were purchased from Abcam (Cambridge, UK). Anti-Src (2109s), anti-phospho-Src (6943s, Tyr416), anti-β-catenin (8480s), anti-phospho β-catenin (5651s, Ser522), and anti-phospho-NF-κB (3033s, Ser536) antibodies were obtained from Cell Signaling Technology (Danvers, MA, USA). Anti-phospho-VE-cadherin (LS-C357312, Tyr731) was purchased from LifeSpan Biosciences (Seattle, WA, USA). Anti-VE-cadherin (sc9989), anti-NF-κB (sc8008), anti-β-actin (sc47778), and anti-GAPDH (sc32233) antibodies were purchased from Santa Cruz Biotechnology (Dallas, TX, USA).
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3

Immunofluorescence Imaging of Neuroinflammatory Markers

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The mice were anesthetized with 1.5% sodium pentobarbital and perfused transcardially with phosphate-buffered saline (PBS), followed by 4% paraformaldehyde (PFA). Their brains were dissected and fixed in 4% PFA for 24 h, and coronal cryosections (30 μm thick) were obtained from the experimental animals. Anti-tau Ser404 (ab92676) and anti-HMGB1 (ab18256) antibodies were purchased from Abcam (Cambridge, United Kingdom), and anti-NLRP3 (AG-20B-0014-C100), anti-ASC (AG-25B-0006-C100), and anti-caspase-1 (P20) (AG-20B-0042-C100) antibodies were purchased from AdipoGen Life Sciences (San Diego, CA, United States) (detailed information in Supplementary Table 1). Fluorescence images were acquired using a laser scanning confocal fluorescence microscope (TCS SP8; Leica, Wetzlar, Germany). The fluorescence images were converted to 8-bit images, and then the stained area was quantified using the ImageJ software. Detection of the background staining was eliminated by setting the same threshold to all the images.
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4

Purification and Characterization of Anthrax Toxin Components

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Recombinant expression and purification of LFn-FlaA was performed as previously described [19 (link)]. B. anthracis protective antigen (PA) and lethal factor (LF) were acquired from List Biologicals. TMRM (T668), Lysotracker (L7528), Sytox Green (S7020), Mitotracker (M7512), Fluo4 (F14217), Pluronic F-127 (P6867), Hoechst 33342 Trihydrochloride Trihydrate (H1399), PI (P3566) and CTB coupled to Alexa 594 (C22842) or 647 (C34778) were purchased from Thermo Scientific. PI solution (556463) and Annexin-V–FITC (556419) were from BD Biosciences. The antibodies used in the study were anti-Caspase-1 (AG-20B-0042-C10, Adipogen), anti-Cathepsin B (31718S, Cell Signaling Technology), anti-Cytochrome c (11940S, Cell Signaling Technology), anti-HMGB1 (ab18256, Abcam), anti-Caspase-3 (9662S, Cell Signaling Technology) and anti-β-Actin-HRP (sc-47778, Santa Cruz Biotechnology), anti-BID (AF860, R&D Systems). Horseradish peroxidase (HRP)-conjugated secondary antibodies were acquired from Jackson Immunoresearch Laboratories and enhanced chemiluminescence solution was from Thermo Scientific. Punicalagin (P0023) was from Sigma Aldrich and the CytoTox 96 Non-Radioactive Cytotoxicity Assay (G1780) and FugeneHD Transfection Reagent were purchased from Promega. Y27632 and (−)-blebbistatin were acquired from Selleckchem. Pam3csk4 (tlrl-pms) and LPS-SM (tlrl-smlps) were acquired from Invivogen.
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