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Organic compounds in which a hydrogen atom or more has been replaced by a halogen atom in an alkane molecule (saturated hydrocarbon chain). Halogen atoms include bromine, chlorine, fluorine, and iodine. Compounds may be in closed ring configurations.
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Aryl Hydrocarbon Receptor Antibody (YA610) is a rabbit-derived, non-conjugated IgG monoclonal antibody, specifically targeting the Aryl Hydrocarbon Receptor. It is for research use only and not intended for patient use.
Rabbit-derived recombinant monoclonal antibody
Targets human Aryl Hydrocarbon Receptor
Validated for Western Blot and Immunocytochemistry/Immunofluorescence
Supplied as a liquid in TBS with BSA, glycerol, and sodium azide preservative
Store at -20°C for up to 1 year
Plays a role in development, immunity, and cancer
Regulates angiogenesis, hematopoiesis, and metabolism
Functions as a ligand-activated transcription factor
Subcellular localization in cytoplasm and nucleus
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Iodocholine iodide is an iodinated quaternary ammonium reagent used as a metabolizable "green" catalyst for free-radical polymerization and as the non-radioactive iodide analogue of C-11 choline for imaging research. Supplied as a white to off-white solid with high, laboratory-grade purity, it is intended for research applications with recommended storage to preserve stability.
Iodinated quaternary ammonium salt suitable for polymerization studies.
Non-radioactive analogue of C-11 choline for PET imaging research.
High purity (≈98%) for consistent experimental results.
Solid, white to off-white appearance for easy handling.
Defined storage conditions to maintain stability.
Available in multiple pack sizes for flexible ordering.
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CADD522 is a small-molecule inhibitor of RUNX2-DNA binding used in research to downregulate RUNX2-mediated transcription. It has demonstrated antiproliferative and antimetastatic effects in cell-based and animal cancer studies and is supplied as a solid for laboratory use.
Inhibits RUNX2-DNA binding with reported IC50 ≈ 10 nM.
Demonstrated activity in in vitro and in vivo cancer models.
High purity appropriate for biochemical and cell-based assays.
Provided in small research quantities for screening and mechanistic studies.
Stable solid form; store at -20 °C under recommended conditions.
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RO8191 is an orally active small-molecule interferon receptor agonist that binds IFNα/β receptor and activates JAK/STAT signalling, showing antiviral activity in HCV replicon assays.
Orally active IFN receptor agonist that activates JAK/STAT and ISG expression.
Shown activity in HCV replicon assays (IC50 ≈ 200 nM) and reported anti-HBV effects.
Chemical formula C14H5F6N5O; molecular weight 373.21 g/mol; CAS 691868-88-9.
Purity reported ~98.8% (datasheet); supplier documentation also lists ≥99.0%.
Store under inert gas at -20°C; in solvent store at -80°C (6 months) or -20°C (1 month) under nitrogen.
Intended for research use only; not for human or veterinary use.
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Beperidium iodide is the iodide salt of a bioactive compound used as a competitive antagonist of acetylcholine receptors. It is supplied as a small, high-purity research reagent with a reported pA2 of 7.93, intended for use as a pharmacological probe in studies of cholinergic signaling.
Competitive antagonist of acetylcholine receptors with reported pA2 = 7.93.
High purity (99.97%) suitable for analytical and experimental use.
Molecular formula C23H34IN3O3 and molecular weight 527.44 g/mol.
Available as a 5 mg research pack for laboratory studies.
Provided as the iodide salt for improved stability and handling.
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