| Cat.No. | Name | Information |
|---|---|---|
| M9887 | Concanavalin A | Concanavalin A is a protein containing only β-sheets in its structure, and belongs to the legume lectins family.It can be used to construct dry eye models, as well as autoimmune hepatitis models. |
| M9797 | 1-Methyl-3-nitro-1-nitrosoguanidine (MNNG) | Methylnitronitrosoguanidine (MNNG) is an alkylating agent with toxic and mutagenic effects. |
| M9616 | Bovine Serum Albumin | Bovine Serum Albumin (BSA) is a globular protein that is used in numerous biochemical applications. |
| M9524 | Lipopolysaccharides | Lipopolysaccharides (LPS) is an endotoxin derived from the outer leaflet of the outer membrane of Gram-negative bacteria. This product is derived from Escherichia coli O55:B5. |
| M9443 | Dextran sulfate sodium salt | Dextran sulfate sodium salt is a polyanionic derivative of dextran produced by esterification of Dextran with chlorosulphonic acid. |
| M9334 | Vancomycin | Vancomycin is a glycopeptide antibiotic as well as a macrocyclic compound that can be used to construct models of bronchiectasis combined with lung infections, as well as for studies related to various bacterial infectious conditions. |
| M9316 | Ceruletide | Ceruletide is a biologically active decapeptide isolated from the skin of the Australian frog Hyla caerulea, acts as a cholecystokinin receptor agonist. |
| M7869 | Kainic acid monohydrate | Kainic acid monohydrate is an agonist at the kainate class of ionotropic glutamate receptors, which induces seizures and neurodegeneration in vivo and is used to induce experimental epilepsy in rodents and study the mechanisms of excitation-induced neuronal apoptosis. |
| M7832 | 6-Hydroxydopamine hydrochloride | 6-Hydroxydopamine hydrochloride is an antagonist of the neurotransmitter dopamine. *The compound is unstable in solutions, freshly prepared is recommended |
| M6894 | L-Arginine | L-Arginine is a endogenous substrate for NOS. |
| M6240 | Angiotensin II human | Angiotensin II human is converted by Angiotensin I through removal of two C-terminal residues by the enzyme angiotensin-converting enzyme (ACE). Angiotensin II is mediated by AT1 and AT2 receptors, which are seven transmembrane glycoproteins with 30% sequence similarity. Keep away from light and prepare for use now. |
| M6209 | Rotenone | Rotenone is an inhibitor of mitochondrial electron transport at NADH:ubiquinone oxidoreductase, and is used to induce a Parkinson-like syndrome as an experimental model in rats. |
| M5688 | Heparin sodium | Heparin sodium salt, a highly sulfated glycosaminoglycan, is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule. |
| M5152 | Sodium Butyrate | Sodium butyrate is the sodium salt of butyric acid, which has been reported to cause hyperacetylation of histones due to its role as a HDAC inhibitor with IC50 values of 0.3, 0.4, 0.3 mM for HDAC1, 2 and 7 respectively. Can be used to construct animal models of venous stenosis. |
| M3699 | Letrozole | Letrozole is an orally active, potent, selective, nonsteroidal, third-generation aromatase (CYP19A1) inhibitor, a synthetic benzyltriazole derivative, which is used in the construction of animal models of polycystic ovary syndrome (PCOS), as well as in studies related to postoperative hormone-responsive breast cancer. |
| M3671 | Cyclophosphamide monohydrate | Cyclophosphamide monohydrate is a nitrogen mustard alkylating agent, it attaches the alkyl group to the guanine base of DNA. *The compound is unstable in solutions, freshly prepared is recommended |
| M3637 | Puromycin dihydrochloride | Puromycin dihydrochloride is an aminonucleoside antibiotic that acts as a protein synthesis inhibitor. |
| M3595 | Gentamicin Sulfate | Gentamicin Sulfate is a broad-spectrum aminoglycoside antibiotic that can be used in cell culture, as well as in the construction of animal models of chronic pelvic inflammatory disease. In addition, Gentamicin sulfate is also a potent DNase I inhibitor with an IC50 value of 0.57 ± 0.12 mM. |
| M2818 | L-NAME hydrochloride | L-NAME hydrochloride is a nonselective inhibitor of nitric oxide synthetases (NOS) for nNOS, eNOS, and iNOS, with Ki of 15 nM, 39 nM and 4.4 μM, respectively. |
| M2227 | Imiquimod | Imiquimod (R837), an imidazoquinoline amine analog to guanosine, is a selective toll like receptor 7 (TLR7) agonist. with potent indirect antiviral activity. |
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