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Α-Chymotrypsin Conjugated to Rhodamine

<strong>α-Chymotrypsin Conjugated to Rhodamine</strong>_x000D_ <strong>Catalog number:</strong> B2013071_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> N/A_x000D_ <strong>Supplied as:</strong> Lyophilized Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> Alpha Chymotrypsin_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: Guo S, Zhao Q, Li Y, Chu S, He F, Li X, Sun N, Zong W, Liu R. Potential toxicity of bisphenol A to α-chymotrypsin and the corresponding mechanisms of their binding Spectrochim Acta A Mol Biomol Spectrosc. 2023 Jan 15;285:121910._x000D_ 2: BARUFFINI A. [alpha-Chymotrypsin] Farmaco Prat. 1959 Oct;14:635-6._x000D_ 3: Kumar A, Venkatesu P. Overview of the stability of α-chymotrypsin in different solvent media Chem Rev. 2012 Jul 11;112(7):4283-307._x000D_ 4: Mukhopadhayay A, Singh D, Sharma KP. Neat Ionic liquid and α-Chymotrypsin-Polymer Surfactant Conjugate-Based Biocatalytic Solvent Biomacromolecules. 2020 Feb 10;21(2):867-877._x000D_ 5: WATTS LF Jr, MARTIN CJ. Stability of alpha-chymotrypsin Arch Ophthalmol. 1961 Jan;65:24-5._x000D_ 6: Sirotkin VA, Kuchierskaya AA. α-chymotrypsin in water-acetone and water-dimethyl sulfoxide mixtures: Effect of preferential solvation and hydration Proteins. 2017 Oct;85(10):1808-1819._x000D_ 7: Ghosh C, Mondal T, Bhattacharyya K. Enzyme activity of α-chymotrypsin: Deactivation by gold nano-cluster and reactivation by glutathione J Colloid Interface Sci. 2017 May 15;494:74-81._x000D_ 8: Gault S, Jaworek MW, Winter R, Cockell CS. High pressures increase α-chymotrypsin enzyme activity under perchlorate stress Commun Biol. 2020 Oct 2;3(1):550._x000D_ 9: Schumann NC, Bruning J, Marshall AC, Abell AD. The role of N-terminal heterocycles in hydrogen bonding to α-chymotrypsin Bioorg Med Chem Lett. 2019 Feb 1;29(3):396-399._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/13758376">10: LAKE LH. Alpha-chymotrypsin in cataract surgery Bull N Y Acad Med. 1961 Jan;37(1):15-26.</a>_x000D_ _x000D_ <strong>Products Related to α-Chymotrypsin Conjugated to Rhodamine can be found at</strong> <a href="https://moleculardepot.com/product-category/Conjugates/"> Conjugates</a>

Product Specifications

Short Description

Catalog Number: B2013071 (1 mg)

Weight

0.8

Length

2

Width

0.9

Height

0.9

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