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Filtered Search Results
Medchemexpress LLC Transthyretin/TTR M 500ug
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The transthyretin/TTR protein is a thyroid hormone binder that may transport thyroxine from the blood to the brain It exists as a homotetramer forming a dimer of dimers with a ligand-regulated central channel suggested to play a role in thyroxine binding and transport Transthyretin/TTR Protein Mouse (HEK293 His) is the recombinant mouse-derived Transthyretin/TTR protein expressed by HEK293 with C-10 His labeled tag
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Medchemexpress LLC Phe-Lys(Trt)-PAB | 1116085-99-4 | 96.2% | 640.81 | C41H44N4O3 | 5 MG
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Phe-Lys(Trt)-PAB is a cathepsin-cleavable peptide-PAB linker used in antibody-drug conjugate (ADC) research. It couples cytotoxic payloads to antibodies via a protease-sensitive spacer that remains stable in circulation and is cleaved by lysosomal cathepsins after internalization to release the payload. Supplied as a 5 mg solid for research use; store as powder at -20°C.
- Cathepsin-cleavable peptide spacer.
- Enables controlled lysosomal release of payloads.
- Stable under physiological conditions.
- High purity suitable for research applications.
- Powder storage at -20°C extends shelf life.
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Ambeed tertButyl 3methylpiperazine1ca
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tert-Butyl 3-methylpiperazine-1-carboxylate, 120737-59-9, 97%
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Medchemexpress LLC M-PEG10-acid | 2409969-94-2 | 98.0% | 500.58 | C22H44O12 | 25 MG
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m-PEG10-acid is a non-cleavable polyethylene glycol (PEG) linker containing 10 ethylene glycol units. It is supplied as an oil and is used as a hydrophilic spacer in the synthesis of antibody-drug conjugates (ADCs) and proteolysis targeting chimeras (PROTACs).
- Non-cleavable 10-unit PEG structure suitable for linker applications.
- Molecular weight 500.58 g·mol⁻¹ and formula C22H44O12.
- Purity 98.0% by NMR.
- Storage at -20°C under nitrogen; in solvent: -80°C (6 months) or -20°C (1 month).
- Available in small research quantities, e.g., 25 mg.
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Cayman Chemical Purmorphamine Other Receptor M
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A 2,6,9-trisubstituted purine that promotes the differentiation of both human and mouse mesenchymal progenitor cells into osteoblasts; binds to and activates the 7-transmembrane Smo receptor of the Hedgehog signaling pathway
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Cell Signaling Technology MORF4L1/MRG15 (D2Y4J) Rabbit mAb 20 ul
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MORF4L1/MRG15 (D2Y4J) Rabbit mAb 20 ul
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Cell Signaling Technology P2X7 Receptor (E1E8T) Rabbit mAb 20 ul
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P2X7 Receptor (E1E8T) Rabbit mAb 20 ul
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Selleck Chemical LLC 740 Y-P
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740 Y-P (PDGFR 740Y-P 740YPDGFR) is a cell-permeable phosphopeptide activator of PI3K
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000435550 TL02-59 1MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000424762 NY-ESO-1 157-165 P 10MG
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eMolecules (4-((2-(2,5-Dimethylphenoxy)ethyl)amino)piperidin-1-yl)(pyridin-4-yl)methanone | 1309241-34-6 | | 100mg
Ambeed | (4-((2-(2,5-Dimethylphenoxy)ethyl)amino)piperidin-1-yl)(pyridin-4-yl)methanone | 100mg | 600830038 | A1362216 | | 1309241-34-6 | | 353.466 | C21H27N3O2
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Cell Signaling Technology SMARCB1/BAF47 (D8M1X) Rabbit mAb 20 ul
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SMARCB1/BAF47 (D8M1X) Rabbit mAb 20 ul
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Chemscene ChemScene | 2,3-Dimethyl-4-nitrophenol | 25G | CS-W017840 | 0.98 | 19499-93-5| MFCD01861284 | 167.16
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ChemScene | 2,3-Dimethyl-4-nitrophenol | 25G | CS-W017840 | 0.98 | 19499-93-5| MFCD01861284 | 167.16
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Medchemexpress LLC N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2-yl)ethyl)phenyl)-2-(pyridin-4-yl)quinazolin-4-amine | 2050747-49-2 | 98.8% | 517.62 g/mol | C32H31N5O2 | 1 ML
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P-gp inhibitor 1 is a research reagent described as a novel small molecule inhibitor that reverses P-glycoprotein-mediated multidrug resistance. It is supplied in solution or solid form for laboratory use, with high purity and defined storage recommendations for stability.
- Potent P-gp inhibition with low cytotoxicity in cell assays.
- Demonstrated activity at low nanomolar EC50 values.
- Available as a 10 mM solution in DMSO or as solid mg quantities.
- High purity suitable for research applications.
- Stable under recommended storage conditions for short- and long-term use.
- Intended for laboratory research use only, not for clinical use.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000403349 - -P-BROMOTETRAMISO 5MG
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