Imidazole (Biotechnology Grade)

<strong>Imidazole (Biotechnology Grade)</strong>_x000D_ <table width="1028">_x000D_ <tbody>_x000D_ <tr>_x000D_ <td width="285">Catalog number:</td>_x000D_ <td width="743">B2010035</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Lot number:</td>_x000D_ <td>Batch Dependent</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Expiration date:</td>_x000D_ <td>Batch Dependent</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Volume/Weight</td>_x000D_ <td>5 g</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Molecular Formula</td>_x000D_ <td>C3H4N2</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Molecular Weight</td>_x000D_ <td>68.08</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>CAS Number</td>_x000D_ <td>288-32-4</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Application:</td>_x000D_ <td>his-tagged protein purification, immobilized metal-affinity chromatography (IMAC)</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Shelf-Life</td>_x000D_ <td>2 years from date of manufacture</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Storage:</td>_x000D_ <td>Room temperature</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Keywords:</td>_x000D_ <td>1,3-Diaza-2,4-cyclopentadiene, Glyoxaline</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Grade</td>_x000D_ <td>Biotechnology grade. All components are highly pure (minimum 99%). All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered on a 0.22 um.</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>References</td>_x000D_ <td width="743">1: Burton RF. Temperature and acid-base balance in ectothermic vertebrates: the_x000D_ imidazole alphastat hypotheses and beyond. J Exp Biol. 2002 Dec;205(Pt_x000D_ 23):3587-600._x000D_ _x000D_ 2: Eseola AO, Obi-Egbedi NO. Spectroscopic study of 2-, 4- and 5-substituents on_x000D_ pKa values of imidazole heterocycles prone to intramolecular proton-electrons_x000D_ transfer. Spectrochim Acta A Mol Biomol Spectrosc. 2010 Feb;75(2):693-701._x000D_ 3: Bhaumik J, Yao Z, Borbas KE, Taniguchi M, Lindsey JS. Masked imidazolyl-_x000D_ dipyrromethanes in the synthesis of imidazole-substituted porphyrins. J Org_x000D_ Chem. 2006 Nov 10;71(23):8807-17._x000D_ _x000D_ 4: Souza GR, Levin CS, Hajitou A, Pasqualini R, Arap W, Miller JH. In vivo_x000D_ detection of gold-imidazole self-assembly complexes: NIR-SERS signal reporters._x000D_ Anal Chem. 2006 Sep 1;78(17):6232-7. doi: 10.1021/ac060483a. PMID: 16944906._x000D_ _x000D_ 5: Ames WM, Larsen SC. DFT calculations of the EPR parameters for Cu(ii) DETA_x000D_ imidazole complexes. Phys Chem Chem Phys. 2009 Oct 1;11(37):8266-74._x000D_ _x000D_ 6: Marboutin L, Desbois A, Berthomieu C. Low-frequency heme, iron-ligand, and_x000D_ ligand modes of imidazole and imidazolate complexes of iron protoporphyrin and_x000D_ microperoxidase in aqueous solution. An analysis by far-infrared difference_x000D_ spectroscopy. J Phys Chem B. 2009 Apr 2;113(13):4492-9._x000D_ _x000D_ 7: Robertson DW, Krushinski JH, Beedle EE, Leander JD, Wong DT, Rathbun RC._x000D_ Structure-activity relationships of (arylalkyl)imidazole anticonvulsants:_x000D_ comparison of the (fluorenylalkyl)imidazoles with nafimidone and denzimol. J Med_x000D_ Chem. 1986 Sep;29(9):1577-86._x000D_ _x000D_ 8: Katsumoto S, Smith SM, Martasek P, Salerno JC. Competition and binding of_x000D_ arginine, imidazole, and aminoguanidine to endothelial nitric oxide synthase:_x000D_ aminoguanidine is a poor model for substrate, intermediate, and arginine analog_x000D_ inhibitor binding. Nitric Oxide. 2003 May;8(3):149-54._x000D_ _x000D_ 9: Schilling S, Niestroj AJ, Rahfeld JU, Hoffmann T, Wermann M, Zunkel K,_x000D_ Wasternack C, Demuth HU. Identification of human glutaminyl cyclase as a_x000D_ metalloenzyme. Potent inhibition by imidazole derivatives and heterocyclic_x000D_ chelators. <a href="https://pubmed.ncbi.nlm.nih.gov/14522962/">J Biol Chem.</a> 2003 Dec 12;278(50):49773-9.</td>_x000D_ </tr>_x000D_ <tr>_x000D_ <td>Related Products</td>_x000D_ <td><a href="https://moleculardepot.com/product-category/buffers/">Biochemical Buffers and Solutions</a></td>_x000D_ </tr>_x000D_ </tbody>_x000D_ </table>