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Filtered Search Results
Medchemexpress LLC CARBONIC ANHYDRASE 2 5UG
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5000194097 CARBONIC ANHYDRASE 2 5UG
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Medchemexpress LLC DM-nitrophen tetrasodium | 291517-40-3 | 90.0% | 561.32 g/mol | C18H19N3Na4O12 | 5 MG
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DM-nitrophen tetrasodium is a photocleavable calcium chelator that releases Ca2+ upon near-ultraviolet illumination, enabling precise temporal control of intracellular calcium levels for signaling studies. The tetrasodium salt improves aqueous solubility for use in biological buffers and is compatible with microinjection and permeabilized cell preparations.
- Photoreleases Ca2+ upon near-ultraviolet illumination.
- Enables rapid, localized increases in free calcium for signaling studies.
- Water-soluble tetrasodium salt compatible with aqueous buffers.
- Suitable for microinjection and use with permeabilized cells.
- Molecular weight 561.32 g/mol; formula C18H19N3Na4O12.
- Supplied in small research quantities for laboratory experiments.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000356058 WSB1 DEGRADER 1 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000410453 N-ETHYLMALEIMIDE 500MG
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Medchemexpress LLC 1,2-dimyristoyl-rac-glycero-3-phosphocholine | 18656-38-7 | MFCD00066562 | ≥98.0% | 677.93 g/mol | C36H72NO8P | 250 MG
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1,2-Dimyristoyl-rac-glycero-3-phosphocholine (DMPC) is a zwitterionic phospholipid used as a simple model of eukaryotic plasma membranes. It readily forms bilayers and liposomes with a neutral surface charge, making it suitable for membrane biophysics, liposome formulation, and studies of lipid-protein interactions where a reproducible, neutral phospholipid matrix is required.
- Forms stable bilayers and liposomes for membrane models.
- Mimics the neutral charge of eukaryotic plasma membranes.
- Suitable for membrane biophysics and lipid-protein interaction studies.
- High purity for reproducible experimental results.
- Available in multiple sizes for small- and large-scale experiments.
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eMolecules S-3-TERT-BUTOXYCARBONYL 5G
5000188851 S-3-TERT-BUTOXYCARBONYL 5G
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Apexbio Technology LLC SU 9516 377090-84-1 5mg
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SU 9516 (CAS 377090-84-1) is a potent and selective inhibitor of cyclin-dependent kinase 2 (CDK2) with an IC50 of 22 nM It exhibits markedly reduced activity against CDK1 CDK4 PKC p38 and PDGFR SU 9516 disrupts cell cycle progression by inhibiting CDK2-mediated phosphorylation of the retinoblastoma protein (pRb) and induces cell cycle arrest and apoptosis in various cancer cell lines including colon carcinoma and leukemia It has been shown to reduce levels of Cyclin D1 and CDK2 promote mitochondrial translocation of Bax cytochrome c release and activate caspase cascades SU 9516 serves as a valuable chemical probe for investigating CDK2 function and cell cycle regulation in cancer research
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Medchemexpress LLC Boc-Met-Leu-Phe-OH | 67247-12-5 | MFCD00037435 | 99.9% | 509.66 | C25H39N3O6S | 25 MG
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Boc-Met-Leu-Phe-OH is a formyl peptide receptor (FPR) antagonist that reduces superoxide production induced by fMLF, with an IC50 of 0.63 μM. It is supplied as a high-purity peptide for research use in studies of FPR signaling and neutrophil activation.
- Reduces fMLF-induced superoxide production (IC50 = 0.63 μM)
- High purity (99.9%)
- Molecular weight 509.66 g/mol
- Molecular formula C25H39N3O6S
- Available in small mg quantities for lab-scale studies
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Medchemexpress LLC Tamra-PEG2-maleimide | 2304558-24-3 | 95.0% | 640.68 g/mol | C35H36N4O8 | 1 MG
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TAMRA-PEG2-Maleimide is a TAMRA-derived fluorescent dye bearing a PEG2 spacer and a maleimide reactive group for selective conjugation to thiol (-SH) groups. Supplied as a solid, it is used for site-specific labeling of cysteine residues, peptides, and other thiol-containing molecules for fluorescence-based assays and imaging.
- Maleimide functional group for selective thiol conjugation.
- TAMRA fluorophore for visible-range fluorescence detection.
- PEG2 spacer improves solubility and reduces steric hindrance.
- High purity suitable for bioconjugation (95.0%).
- Soluble in DMSO at ≥ 100 mg/mL for convenient stock preparation.
- Store protected from light at recommended temperatures for stability.
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eMolecules 1-TERT-BUTOXYCARBONYL-3-I 1G
5000188669 1-TERT-BUTOXYCARBONYL-3-I 1G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000345318 ANIRACETAM 1G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000345319 ANIRACETAM 5G
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Medchemexpress LLC Racemic 3-hydroxyphenylglycine | 31932-87-3 | 99.6% | 167.16 g/mol | C8H9NO3 | 5 MG
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(Rac)-3-Hydroxyphenylglycine is a racemic mixture of the S- and R-enantiomers of 3-hydroxyphenylglycine. The S-enantiomer is reported to act as a potent, selective agonist of the metabotropic glutamate receptor 1 (mGluR1). The material is supplied as an off-white to gray solid for research use and is commonly used in neuroscience and receptor pharmacology studies.
- Racemic mixture of S- and R-enantiomers.
- Potent, selective mGluR1 agonist (activity attributed to the S-enantiomer).
- High purity, suitable for research applications.
- Available in small, milligram-scale quantities for screening.
- Solid form; follow low-temperature storage to maintain stability.
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Medchemexpress LLC N-(2-hydroxyethyl)iminodiacetic acid | 93-62-9 | MFCD00004293 | >=98.0% | 177.16 g/mol | C6H11NO5 | 100 G
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N-(2-Hydroxyethyl)iminodiacetic acid is an amino acid derivative used as a chelating and buffering reagent in laboratory research. It is supplied as a powder for biochemical and analytical applications where metal ion complexation or buffer formulation is required. Identifiers include CAS 93-62-9, formula C6H11NO5, and molecular weight 177.16 g/mol.
- Chelating agent for metal ions including Fe(III)
- Useful as a buffer component in biochemical assays
- Solid powder form convenient for weighing and storage
- Available in multiple pack sizes for laboratory use
- High purity suitable for research (>=98.0%)
- For research use only; not for human or clinical applications
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Apexbio Technology LLC SU 9516 377090-84-1 50mg
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SU 9516 (CAS 377090-84-1) is a potent and selective inhibitor of cyclin-dependent kinase 2 (CDK2) with an IC50 of 22 nM It exhibits markedly reduced activity against CDK1 CDK4 PKC p38 and PDGFR SU 9516 disrupts cell cycle progression by inhibiting CDK2-mediated phosphorylation of the retinoblastoma protein (pRb) and induces cell cycle arrest and apoptosis in various cancer cell lines including colon carcinoma and leukemia It has been shown to reduce levels of Cyclin D1 and CDK2 promote mitochondrial translocation of Bax cytochrome c release and activate caspase cascades SU 9516 serves as a valuable chemical probe for investigating CDK2 function and cell cycle regulation in cancer research
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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