Human CRYGC Protein

<strong>Human CRYGC Protein</strong>_x000D_ <strong>Catalog number:</strong> B2012037_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 µg_x000D_ <strong>Molecular Weight or Concentration:</strong> 23.5 kDa_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20 °C_x000D_ <strong>Keywords:</strong> CCL protein, CRYG3 protein_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: Karahan M, Demirtaş AA, Erdem S, Ava S, Tekeş S, Keklikçi U. Crystalline gene mutations in Turkish children with congenital cataracts Int Ophthalmol. 2021 Aug;41(8):2847-2852._x000D_ 2: Ma Z, Yao W, Theendakara V, Chan CC, Wawrousek E, Hejtmancik JF. Overexpression of human γC-crystallin 5 bp duplication disrupts lens morphology in transgenic mice Invest Ophthalmol Vis Sci. 2011 Jul 23;52(8):5369-75._x000D_ 3: Dixit K, Pande A, Pande J, Sarma SP. Nuclear Magnetic Resonance Structure of a Major Lens Protein, Human γC-Crystallin: Role of the Dipole Moment in Protein Solubility Biochemistry. 2016 Jun 7;55(22):3136-49._x000D_ 4: Guo Y, Su D, Li Q, Yang Z, Ma Z, Ma X, Zhu S. A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree Mol Vis. 2012;18:1874-80. Epub 2012 Jul 11._x000D_ 5: Kandaswamy DK, Vasantha K, Graw J, Santhiya ST. A novel CRYGC E128* mutation underlying an autosomal dominant nuclear cataract in a south Indian kindred Ophthalmic Genet. 2020 Dec;41(6):556-562._x000D_ 6: Liu BF, Song S, Hanson M, Liang JJ. Protein-protein interactions involving congenital cataract T5P gammaC-crystallin mutant: a confocal fluorescence microscopy study Exp Eye Res. 2008 Dec;87(6):515-20._x000D_ 7: Zhong Z, Wu Z, Han L, Chen J. Novel mutations in CRYGC are associated with congenital cataracts in Chinese families Sci Rep. 2017 Mar 15;7(1):189._x000D_ 8: González-Huerta LM, Messina-Baas O, Urueta H, Toral-López J, Cuevas-Covarrubias SA. A CRYGC gene mutation associated with autosomal dominant pulverulent cataract Gene. 2013 Oct 15;529(1):181-5._x000D_ 9: Berry V, Ionides A, Pontikos N, Georgiou M, Yu J, Ocaka LA, Moore AT, Quinlan RA, Michaelides M. The genetic landscape of crystallins in congenital cataract Orphanet J Rare Dis. 2020 Nov 26;15(1):333._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/31523120">10: Zhuang J, Cao Z, Zhu Y, Liu L, Tong Y, Chen X, Wang Y, Lu C, Ma X, Yang J. Mutation screening of crystallin genes in Chinese families with congenital cataracts Mol Vis. 2019 Aug 9;25:427-437. eCollection 2019.</a>_x000D_ _x000D_ <strong>Products Related to Human CRYGC Protein can be found at</strong> <a href="https://moleculardepot.com/product-category/Proteins/"> Proteins</a>