Imidazole Buffer Solution 1.0 M (Biotechnology Grade)

Description

Imidazole buffer Solution 1.0 M
Catalog number: B2010117
Lot number: Batch Dependent
Expiration Date: Batch dependent
Volume/Weight: 50 mL
pH: 6.2-7.8
Supplied as: Ready-to-use solution
Appearance: Clear solution
Applications: reagent component for horseradish peroxidase reactions, chelator for various divalent cations and competitor in the elution of histidine-tagged proteins during NTA purification.
Storage: 2-8°C
Keywords: Glyoxaline solution, Imidazole solution
Grade: Biotechnology grade. All components are highly pure (minimum 99%). All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered on a 0.22 um.

References:
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pKa values of imidazole heterocycles prone to intramolecular proton-electrons
transfer. Spectrochim Acta A Mol Biomol Spectrosc. 2010 Feb;75(2):693-701.
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dipyrromethanes in the synthesis of imidazole-substituted porphyrins. J Org
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4: Souza GR, Levin CS, Hajitou A, Pasqualini R, Arap W, Miller JH. In vivo
detection of gold-imidazole self-assembly complexes: NIR-SERS signal reporters.
Anal Chem. 2006 Sep 1;78(17):6232-7. doi: 10.1021/ac060483a. PMID: 16944906.

5: Ames WM, Larsen SC. DFT calculations of the EPR parameters for Cu(ii) DETA
imidazole complexes. Phys Chem Chem Phys. 2009 Oct 1;11(37):8266-74.

6: Marboutin L, Desbois A, Berthomieu C. Low-frequency heme, iron-ligand, and
ligand modes of imidazole and imidazolate complexes of iron protoporphyrin and
microperoxidase in aqueous solution. An analysis by far-infrared difference
spectroscopy. J Phys Chem B. 2009 Apr 2;113(13):4492-9.

7: Robertson DW, Krushinski JH, Beedle EE, Leander JD, Wong DT, Rathbun RC.
Structure-activity relationships of (arylalkyl)imidazole anticonvulsants:
comparison of the (fluorenylalkyl)imidazoles with nafimidone and denzimol. J Med
Chem. 1986 Sep;29(9):1577-86.

8: Katsumoto S, Smith SM, Martasek P, Salerno JC. Competition and binding of
arginine, imidazole, and aminoguanidine to endothelial nitric oxide synthase:
aminoguanidine is a poor model for substrate, intermediate, and arginine analog
inhibitor binding. Nitric Oxide. 2003 May;8(3):149-54.

9: Schilling S, Niestroj AJ, Rahfeld JU, Hoffmann T, Wermann M, Zunkel K,
Wasternack C, Demuth HU. Identification of human glutaminyl cyclase as a
metalloenzyme. Potent inhibition by imidazole derivatives and heterocyclic
chelators. J Biol Chem. 2003 Dec 12;278(50):49773-9.

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