Prodotti biochimici e reagenti

<p>3-(1-Piperidinyl)-5-[[2-(1-pyrrolidinyl)ethyl]amino]-6H-anthra[1,9-cd]isoxazol-6-one is a chemical compound. It is a potent and selective inhibitor of the aminopeptidase N (APN). APN plays an important role in the degradation of neuropeptides, such as substance P and vasoactive intestinal polypeptide. 3-(1-Piperidinyl)-5-[[2-(1-pyrrolidinyl)ethyl]amino]-6H-anthra[1,9-cd]isoxazol-6-one was shown to inhibit APN activity by binding to its active site.</p>

<p>Please enquire for more information about GSK 591 dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Grams iodine stain is a chemical reagent that is used to detect the presence of bacteria. It can be used on both leaves and human fecal samples. The procedure involves placing a small amount of bacteria on an agar plate. The bacteria are then stained with an iodine solution, which reacts with the fatty acids in the cell walls to produce a black precipitate. This process allows for the detection of bacterial colonies by their black color. The Gram stain is named after the Danish bacteriologist Hans Christian Gram, who developed it in 1884.</p>

<p>ZLDI-8 is a prognostic marker that can be used to predict the response of a patient with non-small-cell lung cancer to chemotherapy. The assay detects the presence of ZLDI-8 protein in cell culture, and can be used to predict the response of a patient with non-small-cell lung cancer to chemotherapy. The level of ZLDI-8 protein in cells is not affected by etoposide treatment, indicating that it is not an oncogene. ZLDI-8 expression is correlated with tumor progression and has been shown to be involved in epithelial mesenchymal transition (EMT). This protein also has potential as an antitumor agent due to its ability to inhibit tumor growth and induce apoptosis through inhibition of angiogenesis, proliferation, and invasion.</p>

<p>NU2058 is a fatty acid that has been shown to inhibit the replication of various viruses. It also inhibits viral infection by binding to and inhibiting the activity of the viral protein NS3 helicase. NU2058 has been shown to have antiviral activity against HIV-1, and it also inhibits human papillomavirus (HPV) infections in vivo. NU2058 is active against some strains of influenza virus and herpes simplex virus type 1 (HSV-1). This compound also inhibits cell proliferation in vitro and restenosis in vivo. In addition, NU2058 has been shown to inhibit breast cancer cells resistant to taxanes or anthracyclines.</p>

<p>MK-0674 is a synthetic compound with anti-tumor activity. It targets the tumor tissue by inhibiting the production of proteins that are vital for cell division. MK-0674 has been shown to be effective in animal studies and clinical trials, but it is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. MK-0674 has also been found to reduce the levels of collagen and nucleophilic carbonyls in cells exposed to oxidative stress, suggesting that it may have anti-oxidant properties. The drug is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>

<p>Thymus peptide C is a peptide that is an inhibitor of Protein interactions. It binds to the receptor and activates the Ligand, which then inhibits ion channels. Thymus peptide C has been used as a research tool to study the inhibition of ion channels in cells. This peptide has also been used as an antibody for the detection of antigens that are associated with cell proliferation.</p>

<p>N-trityl candesartan trityl ester is a peptide that is an activator of the angiotensin receptor, which is a class of G protein-coupled receptors. This compound has been shown to inhibit ion channels and ligand-gated receptors. It also binds to anti-angiotensin II antibody and can be used as a research tool for cell biology.</p>

<p>RNA Binding Motif Protein 3 (RBMY3) is a high-quality research peptide that is commonly used in scientific studies. It is a recombinant protein derived from Escherichia Coli. RBMY3 plays a crucial role in RNA metabolism and regulation, specifically in the binding and processing of RNA molecules. This protein is highly purified and has been extensively tested for its quality and functionality. Researchers rely on RBMY3 to study various cellular processes, including gene expression, mRNA splicing, and post-transcriptional modifications. With its exceptional purity and reliability, RBMY3 is an essential tool for any laboratory conducting cutting-edge research in the field of RNA biology.</p>

<p>A Cholesterol Ester Transfer Protein (CETP) heavy tryptic peptide standard responsible for use in protein identification and quantitation studies. CETP is an enzyme which moves cholesterol esters from high density lipoproteins (HDL) to apolioprotein B-containing particles. This action lowers the amount of HDL which may increase the risk of the disease atherosclerosis.</p>

<p>HEPPSO is a piperazinic buffer with an optimal pH range of 7.1-8.5 and a pKa of 7.84. It is an ampholytic separator, and can bind copper ions.</p>

<p>Monobiotin is a small molecule that is an activator of the L3 receptor. It has been shown to be a ligand for the L3 receptor and to activate this receptor in cells. Monobiotin activates cell membrane ion channels by binding to the L3 receptor and has been used as a research tool to study protein interactions. Monobiotin is also an inhibitor of voltage-gated potassium channels, which are important in regulating excitability in nerve cells, and can serve as a pharmacological tool for studying ion channel function.</p>

<p>EMD 66684 is a vasodilator. It is an antagonist of the angiotensin II type 1 (AT1) receptor, which prevents the release of chemical messengers that would normally constrict blood vessels and increase blood pressure. EMD 66684 has been shown to enhance the release of nitric oxide from vascular endothelial cells and inhibit the production of diacylglycerol. This drug also decreases the synthesis of cyclic guanosine monophosphate, which causes relaxation of smooth muscles in many organs, including the heart and kidneys. EMD 66684 is used to treat cirrhosis and congestive heart failure, as well as clinical conditions such as renovascular hypertension or mesenteric arterial occlusive disease.</p>

<p>Custom research peptide; min purity 95%.</p>

<p>EC 17 is a biological treatment that emits light. It has been shown to have an effect on tumor cells and to increase the immune system's response to cancer. EC 17 activates the antitumor response in various types of cancer cells, including breast, prostate, and colon cancers. EC 17 also exhibits antimicrobial resistance against bacteria such as E. coli and Staphylococcus aureus. The mechanisms of action are not fully understood, but it may be due to its ability to inhibit transcription or DNA replication by binding to bacterial DNA-dependent RNA polymerase or topoisomerase I. EC 17 has been shown to have an effect on symptoms in humans with rheumatoid arthritis when used as an adjuvant therapy for methotrexate treatment. This drug has also been tested in vitro and has been found to inhibit the growth of many types of cancer cells and bacteria, including Mycobacterium tuberculosis.</p>

<p>CU-CPT-8m is a small molecule that has been shown to inhibit the activation of toll-like receptor 4 (TLR4) and TLR2 in monocytes, glomerular inflammation, and renal inflammation. CU-CPT-8m also inhibits the production of pro-inflammatory cytokines and chemokines, such as IL-1β, IL-6, IL-10, and TNFα. CU-CPT-8m has been shown to be both safe and effective in preclinical models of chronic kidney diseases in animal models. CU-CPT-8m may be a promising new option for the treatment of inflammatory kidney diseases.</p>

<p>Mouse Fibronectin ELISA Kit</p>

<p>PF 4778574 is a novel antidepressant drug that belongs to the group of voltage-dependent calcium channel blockers. It has been shown to have neurodevelopmental and neurotrophic properties in vitro, as well as antidepressant effects in animal models. PF 4778574 has also been shown to reduce neuronal cell death induced by glutamate and other excitatory neurotransmitters. The chemical nature of this drug is not yet known, but it may be an l-type calcium channel blocker or a small molecule inhibitor.</p>

<p>Borrelia burgdorferi (Lyme disease) OspA Protein is a highly purified HIS tagged recombinant protein that is derived from E.coli.</p>

<p>Isotype controls are non-reactive immunoglobulins of the same isotype as the primary antibody being used in an application. It is recommended that a non-reactive immunoglobulin of the same isotype and concentration be included as a negative control for each monoclonal antibody reagent used in flow cytometry or other immunoassays.</p>