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Filtered Search Results
Research Products International Corp RPI Cefuroxime, Sodium Salt, 25 Grams
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Cefuroxime Sodium Salt is a second-generation cephalosporin antibiotic. Cefuroxime inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs). This interference disrupts the final stages of peptidoglycan synthesis in the bacterial cell wall, leading to structural instability and eventual cell lysis.
Cefuroxime is effective against a wide spectrum of bacteria, both Gram-positive and Gram-negative. In microbiology and research settings, it is sometimes used as a selective agent in culture media to isolate bacteria that are sensitive to this antibiotic. Additionally, Its inclusion allows for the specific growth of bacteria lacking resistance to cefuroxime.
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Selleck Chemical LLC Spiramycin S4082-50mg
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Spiramycin (Formacidine) is a 16-membered ring macrolide (antibiotic)
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American Radiolabeled Chemicals Inc LINOLEOYL ETH 1-3H 250UC
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Linoleoyl ethanolamide-1-3H 250uCi in ethanol, 1 mCi/ml, S.A. 40-60 Ci/mmol, M.W. 323.0, Shipped in Dry Ice, Exclusive
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Medchemexpress LLC HY-100366 5mg Medchemexpress, Lu AF21934 CAS:1445605-23-1 Purity:>98%
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Medchemexpress, HY-100366 5mg Lu AF21934 CAS:1445605-23-1 Lu AF21934 is a selective and brain-penetrant mGlu4 receptor positive allosteric modulator with an IC 50 of 500 nM for human mGlu4. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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AG Scientific Inc Tetracycline HCl 25 G
Tetracycline hydrochloride is a hydrochloride salt form of the antibiotic tetracycline. This polyketide antibiotic binds to both the 30S and 50S ribosomal subunits, thus inhibiting proper protein synthesis. Although it is capable of binding to both subunits, the binding at the 30S subunit is more pronounced than that at the 50S.Clinically, tetracycline is used as a broad spectrum antibiotic for a variety of Gram-positive and Gram-negative bacterial infections. Conditions which may indicate for tetracycline administration include upper respiratory infection, typhus fever and rikkettsialpox. It can also be administered to treat severe cases of acne.Tetracycline has played a prominent research role in studies of the efficacy of local antibiotic application in cases of dental trauma. Owing to the fluorescent properties of tetracycline and its ability to bind to bone tissue, this antibiotic is also regularly used in bone histomorphometry studies.
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STEMCELL Technologies G418, Size: 250 mg
Antibiotic for selecting transfected mammalian cells
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Medchemexpress LLC HY-111558A 10mg Medchemexpress, Bobcat339 hydrochloride CAS: Purity:>98%
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Medchemexpress, HY-111558A 10mg Bobcat339 HCl CAS: Bobcat339 hydrochloride is a cytosine-based TET enzyme inhibitor with IC50 of 33 μM (TET1) and 73 μM (TET2). It is useful to the field of epigenetics and serves as a starting point for new therapeutics that target DNA methylation and gene transcription. The TET enzymes is responsible for catalyzing the reverse process that is DNA demethylation by recognizing 5-methylcytosine and oxidizing the methyl group via an Fe(II)/alpha-ketoglutarate-dependent mechanism. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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AG Scientific Inc Hygromycin B in Water, 10 ML
The concentration of Hygromycin B in DI water is 100mg/ml. Hygromycin B is an aminoglycoside antibiotic effective against bacteria, fungi, and eukaryotic cells that are isolated from Streptomyces hygroscopicus. It is composed of amino groups attached to glycosides, that bind the 30s ribosomal subunits. This action causes the mRNA sequence to be misread, resulting in protein synthesis inhibition. Hygromycin B is also an antiviral agent, which works as a standard section antibiotic in gene experiments.CAS Number: 31282-04-09Molecular Weight: 527.5 DaChemical Formula: C20H37N3O13Storage Temperature: +4CResearch or further manufacturing use only, not for food or drug use.
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Apexbio Technology LLC Anisomycin 22862-76-6 10mM (in 1mL DMSO)
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Anisomycin is an activator of c-Jun N-terminal kinase (JNK) a stress-activated protein kinase implicated in apoptotic signaling pathways regulating cell proliferation cell cycle progression and apoptosis It activates the JNK pathway at approximately 25 ng/ml concentration Experimental studies demonstrate anisomycin s capability to sensitize apoptosis-resistant cancer cell lines such as DU145 prostate carcinoma cells to Fas-mediated apoptosis as well as to induce apoptosis in leukemic HL-60 cells and primary mouse embryonic fibroblast cells by initiating JNK activation Anisomycin is thus widely utilized as a molecular tool in apoptosis-related research and insight into JNK-associated cell signaling
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Medchemexpress LLC HY-17567B 100mg Medchemexpress, Heparin (Lithium salt) CAS:9045-22-1 Purity:>98%
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Medchemexpress, HY-17567B 100mg Heparin (Lithium salt) CAS:9045-22-1 Heparin Lithium salt is an anticoagulant which binds reversibly to antithrombin III (ATIII). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Enzo Life Sciences Puromycin Aminonucleoside (50mg). CAS: 58-60-6
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A puromycin analog which does not inhibit protein synthesis or induce apoptosis. It is a glomerular epithelial cell toxin which may be used to induce nephropathy in laboratory animals. Alternative name: 3'-Amino-3'-Deoxy-N,N-dimethyladenosine. Purity: ≥98% (TLC). Solubility: Soluble in water (10mg/ml). Long Term Storage: -20°C.
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Ubpbio An ionophore that disrupts mitochondrial membrane potential. Often used for activation of the NLRP3 inflammasome. CAS# 28643-80-3, > 95% purity
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Nigericin sodium salt is an antibiotic derived from Streptomyces hygroscopicus. Functions as an H+, K+, and Pb2+ ionophore. Disrupts mitochondrial membrane potential and activates the NLRP3 inflammasome to induce inflammation.
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Medchemexpress LLC Biotin-PEG6-thalidomide | 2144775-48-2 | MFCD31561114 | 98.3% | C37H53N5O12S | 10MG
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Biotin-PEG6-thalidomide is a biotinylated polyethylene glycol (PEG6)-linked thalidomide derivative used as a PROTAC linker and cereblon (CRBN) affinity probe for targeted protein degradation research. It provides a hydrophilic spacer and a biotin handle to facilitate synthesis, biochemical assays, and affinity-based capture of protein complexes. Supplied for research use only.
- Provides a PEG6 spacer to increase solubility and flexibility
- Contains a thalidomide-derived moiety for cereblon binding
- Includes a biotin tag for affinity capture and pull-down assays
- Suitable for PROTAC synthesis and CRBN-binding studies
- Compatible with common organic solvents and assay conditions
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Medchemexpress LLC HY-102039 10mg Medchemexpress, CDK9-IN-8 CAS:2105956-51-0 Purity:>98%
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Medchemexpress, HY-102039 10mg CDK9-IN-8 CAS:2105956-51-0 CDK9-IN-8 is a highly effective and selective CDK9 inhibitor with an IC50 of 12 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Apexbio Technology LLC CCCP,500mg CAS# 555-60-2
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CCCP (carbonyl cyanide m-chlorophenyl hydrazine) is widely used uncoupler of oxidative phosphorylation.The uncoupler of oxidative phosphorylation blocks ATP synthesis by collapsing the proton motive force.In vitro: A genetic β-galactoside reporter system with a disk diffusion assay on MacConkey Lactose agar petri plates to monitor maintenance of the bacteriophage λ prophage state and viral induction in Escherichia coli K-12. It presented evidence that the phage λ major lytic promoters, pL and pR, are activated via cells containing the reporters following exposure to the energy poison CCCP. Requirement of expression of the λ lytic promoters in response to CCCP is host RecA function and an auto-cleavable CI repressor, as does SOS induction of the λ prophage occurring by a DNA damage-dependent pathway. CCCP-mediated activation of the λ lytic promoters required λ Cro function. CCCP does not modulate an sfi-lacZ SOS reporter [1]. Other sizes are also available. Please inqury us for quote.
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