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Filtered Search Results
Aqua Solutions Isopar G | 90622-57-4 | MFCD01768854 | 20 L
Isopar G | 90622-57-4 | MFCD01768854 | 20 L
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Aqua Solutions Water Saturated Toluene with 25 ml/gal Demulsifier/ASTM D1796, D4007 (4L)
Water Saturated Toluene with 25 ml/gal Demulsifier/ASTM D1796, D4007 (4L)
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Aqua Solutions ISOPAR G 1L
ISOPAR G 1L ..
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Aqua Solutions Isopar G | 90622-57-4 | MFCD01768854 | 500 mL
Isopar G | 90622-57-4 | MFCD01768854 | 500 mL
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Sigma Aldrich Fine Chemicals Biosciences Phenol:Chloroform:Isoamyl Alcohol 25:24:1 Saturated with 10 mM Tris, pH 8.0, 1 mM EDTA| | | 100ml
Phenol:Chloroform:Isoamyl Alcohol 25:24:1 Saturated with 10 mM Tris, pH 8.0, 1 mM EDTA | Purity: | MW: | 0 | 0 | 100ml
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U.S. Pharmacopeia Residual Solvents Mixture - Class 1, 1.2 mL/ampule; 3 ampules
Residual Solvents Mixture - Class 1, 1.2 mL/ampule; 3 ampules (Ozone Depleting Substance)
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Sigma Aldrich Fine Chemicals Biosciences Glycerol, 56-81-5, MFCD00004722, 100 mL
Linear Formula: HOCH2CH(OH)CH2OH, Molecular Weight: 92.09, 99%, BP: 182 °C/20 mmHg, MP: 20 °C, Synonym: 1,2,3-Propanetriol, Glycerin.
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Sigma Aldrich Fine Chemicals Biosciences Glycerol, 56-81-5, MFCD00004722, 500 mL
Linear Formula: HOCH2CH(OH)CH2OH, Molecular Weight: 92.09, Synonym: 1,2,3-Propanetriol, Glycerin, for molecular biology, ≥99.0%. Glycerol is used both in sample preparation and gel formation for polyacrylamide gel electrophoresis. Glycerol (5-10%) increases the density of a sample so that the sample will layer at the bottom of a gel’s sample well. Glycerol is also used to aid in casting gradient gels and as a protein stabilizer and storage buffer component.
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Sigma Aldrich Fine Chemicals Biosciences 26 Lutidine purified by re
26 Lutidine purified by re
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Penta Manufacturing Co 25KG GLYCERIN PURE USP
25kg GLYCERIN PURE USP
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GRAINGER INC 2 6-LUTIDINE 500ML
502781403 2 6-LUTIDINE 500ML
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Medchemexpress LLC 2,6-dimethylpyridin-1-ium-1-olate | 1073-23-0 | MFCD00039715 | >98.0% | 123.15 g/mol | C7H9NO | 5 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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2,6-Lutidine N-oxide is an organic reagent (C7H9NO, MW 123.15 g/mol) commonly used as a ligand, oxidizing agent, and intermediate in organic synthesis and laboratory research. It is typically supplied as a colorless to light yellow liquid with high purity suitable for bench-scale reactions and analytical work.
- High purity suitable for research and synthesis.
- Useful as a ligand and mild oxidizing reagent.
- Compatible with common organic solvents.
- Supplied in small laboratory quantities for convenient handling and storage.
- Identified by CAS 1073-23-0 for unambiguous substance reference.
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Medchemexpress LLC BMT-297376 | 2251031-81-7 | 99.14% | 433.49 | 1 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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BMT-297376 is an optimized Linrodostat and a potent IDO1 inhibitor. This compound appears as a white to off-white solid and is intended for research use only.
- Potent IDO1 inhibitor
- Optimized Linrodostat
- Solid appearance
- White to off-white color
- Suitable for research applications
- Ships at room temperature in continental US
- Store powder at -20°C for 3 years, 4°C for 2 years
- Store in solvent at -80°C for 6 months, -20°C for 1 month
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Medchemexpress LLC Dbet6 Solid/Solv 10Mmx1Ml Dmso | HY-112588-10MM
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Dbet6 Solid/Solv 10Mmx1Ml Dmso
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Medchemexpress LLC Ivaltinostat formic | 98.3% | 473.56 | 50 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Ivaltinostat (CG-200745) formic is an orally active, potent pan-HDAC inhibitor. It features a hydroxamic acid moiety that binds zinc at the bottom of the catalytic pocket. This compound inhibits the deacetylation of histone H3 and tubulin. It also induces the accumulation of p53, promotes p53-dependent transactivation, and enhances the expression of MDM2 and p21 (Waf1/Cip1) proteins. Ivaltinostat formic enhances the sensitivity of Gemcitabine-resistant cells to Gemcitabine and 5-Fluorouracil, induces apoptosis, and exhibits anti-tumour effects.
- Inhibits deacetylation of histone H3 and tubulin
- Induces accumulation of p53 and promotes p53-dependent transactivation
- Enhances expression of MDM2 and p21 (Waf1/Cip1) proteins
- Increases sensitivity of Gemcitabine-resistant cells to Gemcitabine and 5-Fluorouracil
- Induces apoptosis and exhibits anti-tumour effects
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