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Undecyl β-D-maltoside

<strong>Undecyl β-D-maltoside</strong>_x000D_ <strong>Catalog number:</strong> B2013934_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 25 g_x000D_ <strong>Molecular Weight or Concentration:</strong>_x000D_ 496.59 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> −20°C_x000D_ <strong>Keywords:</strong> Undecyl β-D-maltopyranoside_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Perveen S, Khan SB, Malik A, Tareen RB, Nawaz SA, Choudhary MI. Phenolic constituents from Perovskia atriplicifolia Nat Prod Res. 2006 Apr;20(4):347-53._x000D_ 2: Zakharov SD, Savikhin S, Misumi Y, Kurisu G, Cramer WA. Isothermal titration calorimetry of membrane protein interactions: FNR and the cytochrome b(6)f complex Biophys J. 2022 Jan 18;121(2):300-308._x000D_ 3: Amin A, Hariharan P, Chae PS, Guan L. Effect of Detergents on Galactoside Binding by Melibiose Permeases Biochemistry. 2015 Sep 29;54(38):5849-55._x000D_ 4: Wei Y, Li H, Fu D. Oligomeric state of the Escherichia coli metal transporter YiiP J Biol Chem. 2004 Sep 17;279(38):39251-9._x000D_ 5: Joy B, Nishanth Kumar S, Soumya MS, Radhika AR, Vibin M, Abraham A. Embelin (2,5-dihydroxy-3-undecyl-p-benzoquinone): a bioactive molecule isolated from Embelia ribes as an effective photodynamic therapeutic candidate against tumor in vivo Phytomedicine. 2014 Sep 25;21(11):1292-7._x000D_ 6: Ostermeier C, Harrenga A, Ermler U, Michel H. Structure at 2.7 A resolution of the Paracoccus denitrificans two-subunit cytochrome c oxidase complexed with an antibody FV fragment Proc Natl Acad Sci U S A. 1997 Sep 30;94(20):10547-53._x000D_ 7: Kama-Kama F, Omosa LK, Nganga J, Maina N, Osanjo G, Yaouba S, Ilias M, Midiwo J, Naessens J. Antimycoplasmal Activities of Compounds from Solanum aculeastrum and Piliostigma thonningii against Strains from the Mycoplasma mycoides Cluster Front Pharmacol. 2017 Dec 21;8:920._x000D_ 8: Matsushita K, Patel L, Kaback HR. Cytochrome o type oxidase from Escherichia coli. Characterization of the enzyme and mechanism of electrochemical proton gradient generation Biochemistry. 1984 Sep 25;23(20):4703-14._x000D_ 9: Miled N, Riviere M, Cavalier JF, Buono G, Berti L, Verger R. Discrimination between closed and open forms of lipases using electrophoretic techniques Anal Biochem. 2005 Mar 15;338(2):171-8._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/23776025">10: Sakai T, Tanemura Y, Itoh S, Fujimoto Y. Dodecyl -L-rhamnopyranosyl-(12)-_-D-fucopyranoside derivatives from the glandular trichome exudate of Erodium pelargoniflorum Chem Biodivers. 2013 Jun;10(6):1099-108. </a>_x000D_ _x000D_ <strong>Products Related to Undecyl β-D-maltoside can be found at</strong> <a href="https://moleculardepot.com/product-category/Carbohydrates/"> Carbohydrates</a>

Product Specifications

Short Description

Catalog Number: B2013934 (25 g)

Weight

2.6

Length

3.3

Width

1.2

Height

1.2

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