Product Details
Alternative Name: | NOS II, Nitric oxide synthase (inducible) |
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MW: | ~130kDa/subunit; homodimer. |
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Source: | Produced in E. coli. Human iNOS is fused to an N-terminal His-tag. |
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EC: | 1.14.13.39 |
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UniProt ID: | P35228 |
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Formulation: | Liquid. In 50 mM TRIS, pH 7.4, containing 0.1 mM EDTA, 10% glycerol, 100 mM NaCl, 0.1 mM DTT, 10 µM tetrahydrobiopterin. |
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Purity: | ≥90% (SDS-PAGE) |
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Specific Activity: | ≥100 U/mg. 1 U is defined as the amount of enzyme required to produce 1 nmol of NO (nitric o)xide per minute at 37°C. NO synthesis is measured by the conversion of oxyhemoglobin to methemoglobin. |
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Shipping: | Shipped on Dry Ice |
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Long Term Storage: | -80°C |
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Use/Stability: | Stable for at least 1 year after receipt when stored at -80°C. Keep stock vial on ice during experiments. |
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Handling: | Avoid freeze/thaw cycles. After opening, prepare aliquots and store at -80°C. |
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Scientific Background: | Nitric oxide synthases are a family of enzymes catalyzing the production of nitric oxide (NO) from L-arginine. NO is an important cellular signaling molecule. It helps modulate vascular tone, insulin secretion, airway tone, and peristalsis, and is involved in angiogenesis and neural development. It may function as a retrograde neurotransmitter. Nitric oxide is mediated in mammals by the calcium-calmodulin controlled isoenzymes eNOS (endothelial NOS) and nNOS (neuronal NOS). The inducible isoform, iNOS, is involved in immune response, binds calmodulin at physiologically relevant concentrations, and produces NO as an immune defense mechanism, as NO is a free radical with an unpaired electron. It is the proximate cause of septic shock and may function in autoimmune disease. |
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Regulatory Status: | RUO - Research Use Only |
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General Literature References
Expression and localization of nitric oxide synthase isoforms during porcine oocyte growth and acquisition of meiotic competence: E. Chmelikova, et al.; Czech J. Anim. Sci.
54, 137 (2009),
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N(delta)-Methylated L-arginine derivatives and their effects on the nitric oxide generating system: J. Kotthaus, et al.; Bioorg. Med. Chem.
16, 2305 (2008),
Abstract;
Synergistic neuroprotection by bis(7)-tacrine via concurrent blockade of N-methyl-D-aspartate receptors and neuronal nitric-oxide synthase: W. Li, et al.; Mol. Pharmacol.
71, 1258 (2007),
Abstract;
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Use of a murine cell line for identification of human nitric oxide synthase inhibitors: S. Naureckiene, et al.; J. Pharmacol. Toxicol. Meth.
55, 303 (2007),
Abstract;
Endothelial nitric-oxide synthase (type III) is activated and becomes calcium independent upon phosphorylation by cyclic nucleotide-dependent protein kinases: E. Butt, et al.; J. Biol. Chem.
275, 5179 (2000),
Abstract;
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