General Clinical Chemistry Analyzers and Accessories
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Filtered Search Results
GRAINGER INC ETHYL L---LACTATE 25G
502781307 ETHYL L---LACTATE 25G
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Abcam MM-102 (HMTase Inhibitor I x ), 25MG
MW 669.8 Da, Purity >=98%. MM-102 (HMTase Inhibitor IX) is a potent WDR5/MLL interaction inhibitor (IC50 = 2.4 nM). It has been shown to block MLL1 methyltransferase activity, reducing the expression of HoxA9 and Meis-1 genes, which are both critical MLL1 target genes in MLL1 fusion protein-mediated leukemogenesis. WD-repeat protein 5 (WDR5) is a scaffold protein commonly involved in the formation of nucleosome-modifying protein complexes with histones.
The product is subject to the following: Abcam Restricted Use Statement
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Abcam Indo x imod, Indoleamine 2,3-dio x ygenase (IDO) inhibitor, 250MG
MW 218.25 Da, Purity >95%. Methylated tryptophan which acts as an Indoleamine 2,3-dioxygenase (IDO) inhibitor. Prevents T-cell anergy triggered by dendritic cells overexpressing IDO in mice.
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eMolecules 3483-12-3 | Dithiothreitol, biochemical grade | Oakwood Chemical154.240 | C4H10O2S2 | 99.000 | O[C@H](CS)[C@H](O)CS | 5g | 701021355
Dithiothreitol, biochemical grade | Oakwood Chemical | 3483-12-3154.240 | C4H10O2S2 | 99.000 | O[C@H](CS)[C@H](O)CS | 5g | 701021355
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Abcam Apatinib, 25MG
MW 441.9 Da. Potent and selective inhibitor of VEGFR2, IC₅₀ = 1 nm. Orally bioavailable. Achieve your results faster with highly validated, pure and trusted compounds.
The product is subject to the following: Abcam Restricted Use Statement
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Abcam WH-4-023, 25MG
MW 568.7 Da, Purity >98%. Potent and selective inihbitor of the tyrosine kinases Lck and Src with IC₅₀ values of 2 nM for Lck and 6 nM for Src.
The product is subject to the following: Abcam Restricted Use Statement
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Anton Paar Light-scattering instrument for characterizing particlesin liquid dispersions. Measures particle size and transmittance.
Litesizer DLS 101 specificationsMeasurement principle: Dynamic Light Scattering (DLS)Measuring range: 0.3 nm to 10 μm* (particle diameter)Measurement angles: 175°Min. concentration: 0.1 mg/mL (lysozyme)Max. concentration: 50 % w/v (sample-dependent)Min. sample volume: 12 µLAccuracy: Better than +/-2 % on NIST traceable standardsRepeatability: Better than +/-2 % on NIST traceable standardsTransmittance specificationsMeasuring range: 0 % to 100 %Min. sample volume: 15 µLAccuracy: Better than +/-1 %General specificationsLight source: Semiconductor laser diode / 40 mW, 658 nmLaser warm-up time: 6 minTemperature control range: 0 °C to 120 °CAmbient operating temperature: 10 °C to 35 °CHumidity: Up to 80 % non-condensingDimensions: (W, D, H)450 mm, 505 mm, 135 mmWeight:Approx. 18 kg (40 lb)
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Abcam IMR-1, 25MG
MW 353.4 Da, Purity =99%. Notch pathway inhibitor. Achieve your results faster with highly validated, pure and trusted compounds.
The product is subject to the following: Abcam Restricted Use Statement
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Abcam 7-(Diethylamino)coumarin-3-carbonyl azide, 25MG
MW 286.29 Da, Purity >95%. Aldehyde and ketone reactive probe. Suitable for labeling proteins and other carbonyl-containing molecules. Ceramides can be derivatized using 7-(diethylamino)coumarin-3-carbonyl azide with subsequent gradient HPLC separation allowing sensitive optical quantification of individual cellular ceramides. Suitable for use in HPLC labeling of lipids and alkylcycloketones.
The product is subject to the following: Abcam Restricted Use Statement
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Abcam SP-2509, LSD1 inhibitor, 5MG
MW 437.9 Da, Purity >98%. Potent, selective (IC₅₀ = 13 nM) and reversible inhibitor of the histone demethylase LSD1 (KDM1A). No activity against MAO-A, MAO-B, lactate dehydrogenase and glucose oxidase.
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Abcam Adaphostin, 5MG
MW 393.5 Da, Purity >=98%. Adaphostin is a p210bcr/abl tyrosine kinase inhibitor (IC50 = 14 μM) that displays anti-proliferative activity in leukemia models, human prostate cancer cell line PC-3 and other cancer cell lines. Adaphostin is a potent inducer of myeloid cell death.
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Abcam Prostaglandin A1, 5MG
MW 336.5 Da. Endogenous prostaglandin with diverse biological actions including anti-hypertensive, anti-inflammatory, anti-viral and anti-cancer properties.
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Abcam Capivasertib (AZD5363), 100MG
MW 428.9 Da, Purity >95%. A novel pyrrolopyrimidine derivative. A potent inhibitor of all AKT isoforms, IC₅₀ <10 nM, with potential antineoplastic activity.
The product is subject to the following: Abcam Restricted Use Statement
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