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Filtered Search Results
Medchemexpress LLC 7-morpholin-4-yl-benzo[1,2,5]oxadiazol-4-ylamine | 842964-18-5 | MFCD03422529 | 98.0% | 220.23 g/mol | C10H12N4O2 | 10MM 1ML
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Delta-Secretase Inhibitor 11 (CAS 842964-18-5) is a small-molecule research compound that inhibits δ-secretase activity. It is supplied as a 10 mM solution in a 1 mL vial and is used as a biochemical tool to probe delta-secretase-related pathways. The compound has molecular formula C10H12N4O2 and a molecular weight of 220.23 g/mol.
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Medchemexpress LLC Lyn peptide inhibitor | 222018-18-0 | 99.4% | 2370.88 | 5 MG
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Lyn peptide inhibitor is a potent and cell-permeable inhibitor of the Lyn-coupled IL-5 receptor signaling pathway, while keeping other signals intact. It blocks Lyn activation and inhibits the binding of Lyn tyrosine kinase to the βc subunit of IL-3/GM-CSF/IL-5 receptors. It can be used for the study of asthma, allergic, and other eosinophilic disorders.
- Potent and cell-permeable inhibitor
- Blocks Lyn activation
- Inhibits binding of Lyn tyrosine kinase to the βc subunit of IL-3/GM-CSF/IL-5 receptors
- Used for the study of asthma
- Used for the study of allergic disorders
- Used for the study of other eosinophilic disorders
- Appearance: White to off-white solid
- Powder storage: -80°C for 2 years, -20°C for 1 year (sealed, away from moisture)
- In solvent storage: -80°C for 6 months, -20°C for 1 month (sealed, away from moisture)
- Soluble in DMSO (5 mg/mL)
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Medchemexpress LLC ICL-CCIC-0019 5mg | 936498-64-5 | 572.46 g·mol⁻1 | C26H44Br2N4 | 5 MG
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ICL-CCIC-0019 is a small-molecule inhibitor of choline kinase α (CHKα) used in research to modulate phospholipid metabolism and induce cell-cycle arrest and apoptosis in cancer cell lines. Supplied as a solid for laboratory research use only.
- Purity 97.8% by supplier certificate of analysis.
- Molecular weight 572.46 g·mol⁻1.
- Chemical formula C26H44Br2N4.
- Soluble in DMSO: 8.33 mg/mL (approx. 14.55 mM); ultrasonic recommended.
- Appearance white to off-white solid.
- Storage sealed, away from moisture and light; in solvent: -80°C (6 months) or -20°C (1 month).
- Packaged as a 5 MG research vial.
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Medchemexpress LLC LDN-91946 | 439946-22-2 | 98.0% | 1 ML
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LDN-91946 is a potent, selective, and uncompetitive ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitor with a Ki app of 2.8 μM. It is intended for research use only. The compound is inactive against UCH-L3 at 20 μM and shows no activity against TGase 2, Papain, and Caspase-3 at 40 μM. It also exhibits no cytotoxicity in serum-starved Neuro 2A (N2A) cells at concentrations up to 0.1 mM.
- Potent, selective, and uncompetitive UCH-L1 inhibitor
- Ki app of 2.8 μM (UCH-L1)
- Inactive against UCH-L3 at 20 μM
- No activity against TGase 2, Papain, and Caspase-3 at 40 μM
- No cytotoxicity in serum-starved Neuro 2A (N2A) cells up to 0.1 mM
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Perkin Elmer US LLC BOLT PROBE
BOLT PROBE
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Neuromics, Inc 250 ml bottle of BioLock Solution
250 ml bottle of BioLock Solution (Biotin blocking solution for lysates and culture supernatants) yellowish-brown liquid
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Aqua Solutions Silver Nitrate 0.1000 +- 0.0005 Normal In 2-propanol N.i.s.t. Traceable Prepared To Astm D 3227 (4l)
Silver Nitrate 0.1000 +- 0.0005 Normal In 2-propanol N.i.s.t. Traceable Prepared To Astm D 3227 (4l)
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Chemgenes Corporation CHEMGENES CORPORATION
NC3940870 DDTT SOLUTION 0.05SULFURIZING
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Hampton Research HR2-902-07/StockOptions HEPES #07 pH 7.4, 185 ml
HR2-902-07/StockOptions HEPES #07 pH 7.4, 185 ml. Please note items from this supplier are non-returnable.
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Aqua Solutions DBA/ 0-Xylene Reagent (1.7 Normal Dibutylamine) (4L)
DBA/ 0-Xylene Reagent (1.7 Normal Dibutylamine) (4L)
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Medchemexpress LLC CASPASE-3/7 INHIBITO 5 mg
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CASPASE-3/7 INHIBITO 5MG
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Cayman Chemical SodIM Phosphate Stock SolutI
A concentrated buffer solution
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Cayman Chemical SodIM Phosphate Stock SolutI
A concentrated buffer solution
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Cayman Chemical SodIM Phosphate Stock SolutI
A concentrated buffer solution
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ABclonal Technology RNase Inhibitor, Mammalian
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RNase Inhibitor, Mammalian specifically inhibits RNases A, B and C. It inhibits RNases by binding noncovalently in a 1:1 ratio with high affinity. It is not effective against RNase 1, RNase T1, S1 Nuclease, RNase H or RNase from Aspergillus. In addition, no inhibition of polymerase activity is observed when RNase Inhibitor is used with Taq DNA Polymerase, AMV or M-MuLV Reverse Transcriptases, or Phage RNA Polymerases (SP6, T7, or T3). The 50 kDa protein inhibits RNases by binding noncovalently in a 1:1 ratio with an association constant greater than 1014.
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