General Clinical Chemistry Analyzers and Accessories
Roche Diagnostics Cleaner Alkaline Bio HT, System reagent for the Cedex Bio HT Analyzer | 200 runs
Cleaner Alkaline Bio HT, System reagent for the Cedex Bio HT Analyzer200 runs
Alkali Scientific Sample Cup for Abott Architect Series Analyzers, Polystyrene, 20x49mm, 4,000/Case
Polystyrene Sample Cup, 20 × 49 mm — For Abbott Architect Series Analyzers These premium sample cups are manufactured from high clarity polystyrene and are engineered specifically for Abbott Architect Series analyzers. With precise 20 × 49 mm dimensions, they ensure an exact fit within analyzer racks and automation systems, supporting accurate and efficient clinical chemistry and immunoassay workflows. The rigid polystyrene construction provides excellent optical clarity for easy visual verification of sample volume and quality, while maintaining tight dimensional tolerances to reduce instrument errors and ensure smooth sample handling. Key Features: Designed for Abbott Architect Series analyzers 20 × 49 mm ensures a secure and precise fit Made from high clarity polystyrene for easy visual inspection Smooth interior for complete sample recovery and accurate pipetting Disposable, non pyrogenic, and free of RNase/DNase Ideal for clinical chemistry and immunoassay sample process.
Roche Diagnostics CEDEX BIO LDH
This product is intended for quantitative determination of lactate dehydrogenaase (LDH) activity in aqueous solution using the Cedex Bio Instrument.
Abcam CHIR-124, 50MG
MW 419.9 Da, Purity >98%. Novel and potent Chk1 inhibitor (IC₅₀ = 0.3 nM), 2,000-fold more potent than Chk2 (IC₅₀ = 0.7 μM). Also, potently targets other kinases such as FLT3 (IC₅₀ = 5.8 nM), PDGFR (IC₅₀ = 6.6 nM), GSK-3 (IC₅₀ = 23.3 nM) and Fyn (IC₅₀ = 98.8 nM) .
The product is subject to the following: Abcam Restricted Use Statement
Abcam SB742457 (Intepirdine), 5-HT6 antagonist, 5MG
MW 353.4 Da. Potent (pKi = 9.63) and highly selective 5-HT6 antagonist. Greater thsan 100-fold selective against other receptors. Reverses learning impairment in animal models.
The product is subject to the following: Abcam Restricted Use Statement
Abcam GW-311616A, 5MG
MW 434 Da, Purity >=98%. A potent and selective intracellular neutrophil elastase (NE, alpha-1-proteinase) inhibitor. Inhibits human neutrophil elastase (HNE) and is selective over other human serine proteases with IC₅₀ values of 22 nM for HNE, >100 μM for trypsin, cathepsin G and plasmin, >3 μM for chymotrypsin and tissue plasminogen activator.
The product is subject to the following: Abcam Restricted Use Statement
Abcam Alvespimycin (17-DMAG) hydrochloride, 100MG
MW 653.2 Da, Purity >99%. A potent Hsp90 inhibitor (IC₅₀ = 62 nM), can bind to the ATP-binding motif and inhibit the protein chaperoning activity.
The product is subject to the following: Abcam Restricted Use Statement
Abcam BIIB 021, 25MG
MW 318.76 Da, Purity >98%. Selective, Hsp90 competitive inhibitor (Ki = 1.7 nM). Displays no significant activity at a range of ATP-binding kinases or Na+K+ ATPase. Induces degradation of HER-2 in vitro (EC₅₀ = 38 nM in MCF-7 cells). Inhibits growth and promotes cell death in a variety of human tumor cells. Orally bioavailable.
The product is subject to the following: Abcam Restricted Use Statement
Abcam Dovitinib, class III-V receptor tyrosine kinase inhibitor, 5MG
MW 392.4 Da, Purity >99%. Potent, selective inhibitor of class III-V receptor tyrosine kinases (RTKs). Inhibits FLT3 (IC₅₀ = 1 nM), c-KIT (IC₅₀ = 2 nM), FGFR (IC₅₀ = 8 nM), VEGFR1/2/3 (IC₅₀ values are 10 nM, 13 nM and 8 nM respectively), PDGFRβ (IC₅₀ = 27 nM), and CSF-1R (IC₅₀ = 36 nM). Selectively blocks growth of B9 cells transformed by wild type, or activated mutant FGFR3. Induces apoptosis, or sensitizes cells to induction of apoptosis by other means in a variety of cancer cell lines.
The product is subject to the following: Abcam Restricted Use Statement
Abcam CCT-251921, 5MG
MW 410.9 Da, Purity >=98%. CCT-251921 is a potent, selective, small-molecule modulator of the mediator complex-associated kinases CDK8 and CDK19 (IC₅₀, CDK8 = 2.3 nM; CDK19 = 2.6 nM).
The product is subject to the following: Abcam Restricted Use Statement
AdipoGen 3-Butyn-2-ol
Chemical. CAS 2028-63-9. Formula C4H6O. MW 70.09. Synthetic. Organic building block. 3-Butyn-2-ol is an intermediate used to prepare aminoindanes with inhibitory activity toward acetylcholine esterase and monoamine oxidase useful as anti-Alzheimer’s agents.
AdipoGen Bestatin hydrochloride
Chemical. CAS 65391-42-6. Formula C16H24N2O4 . HCl. Molecular Weight 308.4 . 36.5. Antibiotic. Potent, competitive and specific aminopeptidase inhibitor. Can be administered in vitro to cultured cells or in vivo with low toxicity. Inhibits aminopeptidase B, aminopeptidase N, leucine aminopeptidase and the aminopeptidase activity of leukotriene A4 LTA4 hydrolase. It is selective for these aminopeptidases over aminopeptidase A, trypsin, chymotrypsin, elastase, papain, pepsin and thermolysin. Immunomodulator. Displays immunostimulant activity via activation of macrophages and T lymphocytes. Displays anticancer and anti-inflammatory activity. Shown to inhibit proliferation, migration and invasion, and induces autophagy and apoptosis in cancer cells. Inhibits the production of LTB4 in erythrocytes.