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Filtered Search Results
Electron Microscopy Sciences Sodium Phosphate 1% Aqueous 500 ML
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Used in Fat Stains in Supersaturated Alcohol for fat and lipid stain. See Lillie, R.D.,Histopathologic Technical and Practical Histochemistry, 3rd edition, McGraw-Hill, NY, 1965 or Clark, G., (ed) Staining Procedures, 3rd edition, Williams & Wilkins, Baltimore, p. 149, c. 1973
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Sigma Aldrich Fine Chemicals Biosciences KitAlysis High-Throughput 24 Pd Precatalyst Reaction Screening Kit-Pack of 2
Screening kit for cross-coupling reactions. Each kit contains 2 customizable screening sets that include the following components: 24 pre-weighed catalysts in glass micro vials loaded with stir bars and topped with cap mat. 2 KitAlysis 24-Well reaction block replacement films. 4 empty substrate stock solution reaction vials with stir bars. 3 stir bars for stock solutions. 1 internal standard.
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Sigma Aldrich Fine Chemicals Biosciences Guaiacol oxidation indicator | 90-05-1 | MFCD00002185 | 100G
Guaiacol oxidation indicator | Purity: >=98.0% | Mol Wt: 124.14 | 90-05-1 | MFCD00002185 | 100G
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eMolecules Broadpharm / Propargyl-PEG6-Ms / 250mg / 393649417 / BP-24026 / 98.000 / 1036204-62-2 / MFCD20134135 / 354.410 / C14H26O8S
Broadpharm / Propargyl-PEG6-Ms / 250mg / 393649417 / BP-24026 / 98.000 / 1036204-62-2 / MFCD20134135 / 354.410 / C14H26O8S
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Medchemexpress LLC β-secretase inhibitor IV | 797035-11-1 | MFCD09037559 | >98.0% | 578.72 g/mol | C31H38N4O5S | 5 MG
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β-Secretase Inhibitor IV is a cell-active small-molecule inhibitor of BACE-1 (β-secretase) used in research on amyloid precursor protein processing and Alzheimer's disease pathways. It shows low-nanomolar biochemical potency (IC50 = 15.6 nM at 2 nM BACE-1; 16.3 nM at 100 pM BACE-1). Chemical identifiers: C31H38N4O5S; MW 578.72 g/mol; CAS 797035-11-1.
- Potent inhibition at low nanomolar concentrations.
- Demonstrated cell activity in cell-based assays.
- Suitable for in vitro and cell-based BACE-1 studies.
- High purity material (>98%) available for research.
- Small-molecule format compatible with standard assay workflows.
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LaMarKa Chemical Company Ferric Chloride 0.2% W/V, 1l
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Ferric Chloride 0.2% W/V, 1l Plastic Bottle
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Electron Microscopy Sciences Sodium Thiosulfate, 0.2% Aqueous 500 ML
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Used in combined Hematoxylin and Eosin/Methenamine Silver Stain for the fungi in tissue Sections. For bacterial, fungal stains. See references: Lamps, Laura W. et al A Combined Hematoxylin and Eosin/Methenamin Silver Stain for theHistological Diagnosis of Fungi In Tissue Sections., J. of Histotechnology 23:4 p.341 – 345, 2000.
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Pickering Laboratories Inc Artificial Perspiration, AATCC TM 15, Custom pH, Stabilized, each (200 mL/bottle)
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Perspiration is on everything we touch with our fingers or that comes into contact with our bodies. Sweat can react with materials and trigger allergies, or it can shorten product service life via corrosion or discoloration. Natural human perspiration has a complex composition that depends on the type of sweat gland, the person’s metabolism and hydration level. This solution is used to determine the colorfastness of textiles to the effects of acid perspiration according to Test Method 15. The same formulation is also used to determine colorfastness to a combination of light and perspiration accoreding to Test Method 125. It is applicable to dyed, printed or otherwise colored textile fibers, yarns and fabrics of all kinds. This formulation can also be used for the testing of dyestuffs as applied to textiles. Provided at a pH level of your choosing
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Electron Microscopy Sciences Ferric Ammonium Sulfate 5% Aqueous 500 ML
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It is available for your convenience in a concentration of 5.0% aqueous.
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Selleck Chemical LLC LDN-212854
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LDN-212854 (BMP Inhibitor III) is a potent and selective BMP receptor inhibitor with IC50 of 1 3 nM for ALK2 about 2- 66- 1641- and 7135-fold selectivity over ALK1 ALK3 ALK4 and ALK5 respectively
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Medchemexpress LLC ICL-CCIC-0019 10mg | 936498-64-5 | 572.46 g/mol | C26H44Br2N4 | 10 MG
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ICL-CCIC-0019 is a small-molecule inhibitor of choline kinase α (CHKα) used in preclinical cancer research. It decreases phosphocholine levels and induces G1 cell-cycle arrest, endoplasmic reticulum stress, and apoptosis in cancer cell lines.
- Inhibits choline kinase α (CHKα) activity.
- Induces G1 cell-cycle arrest and apoptosis in cancer cell lines.
- Confirmed purity by HPLC: 95.38%.
- Provided as a dibromide pyridinium salt (C26H44Br2N4).
- Store sealed at -20°C; in solvent, store at -80°C up to 6 months.
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Medchemexpress LLC Cathepsin G inhibitor I | 429676-93-7 | MFCD28137715 | >99.0% | 620.63 g/mol | C36H33N2O6P | 1 MG
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Cathepsin G Inhibitor I is a selective, reversible, competitive, non-peptide inhibitor of cathepsin G used for biochemical and cellular research to inhibit cathepsin G activity.
- Selective reversible competitive inhibitor of cathepsin G (IC50 = 53 nM; Ki = 63 nM).
- High purity solid, white to off-white, suitable for analytical and bioassay work.
- Molecular formula C36H33N2O6P; molecular weight 620.63 g/mol.
- Recommended storage: sealed, away from moisture and light; in solvent: -80°C up to 6 months, -20°C up to 1 month.
- Suitable for biochemical assays and cellular studies to probe cathepsin G function.
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Medchemexpress LLC Human PD-L1 inhibitor I | 2135542-86-6 | 98.9% | 2350.58 | 10 MG
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Human PD-L1 inhibitor I is a hPD-1 peptide ligand with a KD of 3.39 μM. It may disturb the binding of hPD-L1 to hPD-1.
- hPD-1 peptide ligand
- KD of 3.39 μM
- May disturb the binding of hPD-L1 to hPD-1
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Medchemexpress LLC Tie2 kinase inhibitor 1 | 948557-43-5 | 439.53 g/mol | C26H21N3O2S | 100 MG
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Tie2 kinase inhibitor 1 is a selective small-molecule inhibitor of the Tie2 (TEK) receptor tyrosine kinase, reported to inhibit Tie2 with an IC50 of approximately 250 nM and to exhibit anti-cancer activity in preclinical studies. The compound is supplied as a solid and is intended for use in biochemical and cellular research to probe Tie2-dependent signaling pathways.
- Potent, selective Tie2 inhibition (IC50 ≈ 250 nM).
- Suitable for biochemical kinase assays and cellular studies.
- Reported anti-cancer activity in preclinical models.
- Solid form with defined storage recommendations for stability.
- Characterized by CAS 948557-43-5 and molecular weight 439.53 g/mol.
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Medchemexpress LLC Deschloroetizolam | 40054-73-7 | MFCD02942552 | 99.8% | 308.41 g/mol | C17H16N4S | 5 MG
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Deschloroetizolam is a thienotriazolodiazepine provided as a research and analytical reference material for laboratory and forensic applications. The product is documented with CAS 40054-73-7, molecular formula C17H16N4S, and molecular weight 308.41 g/mol. It is offered in solid and solution formats and is accompanied by a datasheet and SDS; confirm lot-specific certificate of analysis for exact purity and specifications.
- High reported purity suitable for analytical workflows.
- Available in small solid quantities and pre-made solutions for convenience.
- Accompanied by a downloadable datasheet and safety data sheet.
- Documented molecular formula and molecular weight for traceability.
- Intended for laboratory and forensic research use only.
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