| Cat.No. | Name | Information |
|---|---|---|
| M21440 | Sodium iodate | Sodium iodate is an inorganic compound with the chemical formula NaIO3 and can be used as an oxidant. |
| 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. |
| M6033 | Dihydrotestosterone | Dihydrotestosterone is an androgen (male hormone). Specifically it's the strongest of the androgens. It can be used to construct animal models of polycystic ovary syndrome (PCOS). |
| M6004 | Testosterone propionate | Testosterone Propionate is a potent anabolic steroid used in the study of low testosterone level disorders, where it is an agonist of the androgen receptor (AR). In addition, Testosterone Propionate is also used in the construction of animal disease models (e.g. rat prostate hyperplasia model, rat seborrheic alopecia rat model, etc.). |
| M5791 | Mitomycin C | Mitomycin C (Ametycine) is an antineoplastic antibiotic by inhibiting DNA synthesis. |
| 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. |
| M5368 | 4-Aminopyridine | 4-Aminopyridine is a nonselective K+ channel blocker that binds from the cytoplasmic side of the cell membrane. |
| 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. |
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