This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.
product summary
company name :
MilliporeSigma
other brands :
FLUKA, Sigma-Aldrich, Roche Applied Science
product type :
protein
product name :
β-Galactosidase from Escherichia coli
catalog :
G3153
citations: 98
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Hetta M, Aly H, All N. Estimation of resveratrol content in peanut pericarp and its relation to the in vitro inhibitory activity on carbohydrate metabolizing enzymes. Pharmazie. 2014;69:92-5 pubmed
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Azad A, Bukczynska P, Jackson S, Haupt Y, Haput Y, Cullinane C, et al. Co-targeting deoxyribonucleic acid-dependent protein kinase and poly(adenosine diphosphate-ribose) polymerase-1 promotes accelerated senescence of irradiated cancer cells. Int J Radiat Oncol Biol Phys. 2014;88:385-94 pubmed publisher
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Sánchez Pérez Y, Chirino Y, Osornio Vargas A, Herrera L, Morales Bárcenas R, López Saavedra A, et al. Cytoplasmic p21(CIP1/WAF1), ERK1/2 activation, and cytoskeletal remodeling are associated with the senescence-like phenotype after airborne particulate matter (PM(10)) exposure in lung cells. Toxicol Lett. 2014;225:12-9 pubmed publisher
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Hwang B, Pan J, Kim B, Kim J. Functional display of active tetrameric beta-galactosidase using Bacillus subtilis spore display system. J Nanosci Nanotechnol. 2013;13:2313-9 pubmed
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Kriazhevskih N, Demkina E, Loĭko N, Baslerov R, Kolganova T, Soina V, et al. [Comparison of the adaptation potential of Arthrobacter oxydans and Acinetobacter lwoffii isolated from permafrost sediments with their collection analogues]. Mikrobiologiia. 2013;82:27-41 pubmed
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Zhang X, Wang Q, Chen B, Wei Q, Xu C, Jiang R, et al. [Angelica sinensis polysaccharides delay aging of hematopoietic stem cells through inhibitting oxidative damge]. Zhongguo Zhong Yao Za Zhi. 2013;38:407-12 pubmed
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Dai W, Yang C, Luo F, Li S, Huang R, Xie Y, et al. [Establishment of recombinant Lac Z reporter gene-transformed yeast cells for bioassay of androgen-like compounds in environment]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2013;29:303-9 pubmed
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Zhang C, Sun K, Geng S, Liu D, Zhang X, Liu J, et al. [Mechanism of hematopoietic stem/progenitor cell aging induced by radiation damage]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2013;29:233-6 pubmed
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Gort L, Santamaria R, Grinberg D, Vilageliu L, Chabas A. Identification of a novel pseudodeficiency allele in the GLB1 gene in a carrier of GM1 gangliosidosis. Clin Genet. 2007;72:109-11 pubmed
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Santamaria R, Blanco M, Chabas A, Grinberg D, Vilageliu L. Identification of 14 novel GLB1 mutations, including five deletions, in 19 patients with GM1 gangliosidosis from South America. Clin Genet. 2007;71:273-9 pubmed
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Santamaria R, Chabas A, Coll M, Miranda C, Vilageliu L, Grinberg D. Twenty-one novel mutations in the GLB1 gene identified in a large group of GM1-gangliosidosis and Morquio B patients: possible common origin for the prevalent p.R59H mutation among gypsies. Hum Mutat. 2006;27:1060 pubmed
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Bauer W, Talmadge K, Keegstra K, Albersheim P. The Structure of Plant Cell Walls: II. The Hemicellulose of the Walls of Suspension-cultured Sycamore Cells. Plant Physiol. 1973;51:174-87 pubmed
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Muzny D, Scherer S, Kaul R, Wang J, Yu J, Sudbrak R, et al. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 2006;440:1194-8 pubmed
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Tatano Y, Takeuchi N, Kuwahara J, Sakuraba H, Takahashi T, Takada G, et al. Elastogenesis in cultured dermal fibroblasts from patients with lysosomal beta-galactosidase, protective protein/cathepsin A and neuraminidase-1 deficiencies. J Med Invest. 2006;53:103-12 pubmed
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Lewandrowski U, Moebius J, Walter U, Sickmann A. Elucidation of N-glycosylation sites on human platelet proteins: a glycoproteomic approach. Mol Cell Proteomics. 2006;5:226-33 pubmed
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Roze E, Paschke E, Lopez N, Eck T, Yoshida K, Maurel Ollivier A, et al. Dystonia and parkinsonism in GM1 type 3 gangliosidosis. Mov Disord. 2005;20:1366-9 pubmed
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Gururaj A, Sztriha L, Hertecant J, Johansen J, Georgiou T, Campos Y, et al. Magnetic resonance imaging findings and novel mutations in GM1 gangliosidosis. J Child Neurol. 2005;20:57-60 pubmed
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Caciotti A, Donati M, Boneh A, D AZZO A, Federico A, Parini R, et al. Role of beta-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis. Hum Mutat. 2005;25:285-92 pubmed
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Gerhard D, Wagner L, Feingold E, Shenmen C, Grouse L, Schuler G, et al. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. 2004;14:2121-7 pubmed
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Georgiou T, Drousiotou A, Campos Y, Caciotti A, Sztriha L, Gururaj A, et al. Four novel mutations in patients from the Middle East with the infantile form of GM1-gangliosidosis. Hum Mutat. 2004;24:352 pubmed
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Monod J, Cohn M. [Biosynthesis induced by enzymes; enzymatic adaptation]. Adv Enzymol Relat Subj Biochem. 1952;13:67-119 pubmed
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Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, et al. Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat Genet. 2004;36:40-5 pubmed
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Landman O. Properties and induction of beta-galactosidase in Bacillus megaterium. Biochim Biophys Acta. 1957;23:558-69 pubmed
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Caciotti A, Bardelli T, Cunningham J, D AZZO A, Zammarchi E, Morrone A. Modulating action of the new polymorphism L436F detected in the GLB1 gene of a type-II GM1 gangliosidosis patient. Hum Genet. 2003;113:44-50 pubmed
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Bagshaw R, Zhang S, Hinek A, Skomorowski M, Whelan D, Clarke J, et al. Novel mutations (Asn 484 Lys, Thr 500 Ala, Gly 438 Glu) in Morquio B disease. Biochim Biophys Acta. 2002;1588:247-53 pubmed
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Paschke E, Milos I, Kreimer Erlacher H, Hoefler G, Beck M, Hoeltzenbein M, et al. Mutation analyses in 17 patients with deficiency in acid beta-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type B. Hum Genet. 2001;109:159-66 pubmed
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Hinek A, Zhang S, Smith A, Callahan J. Impaired elastic-fiber assembly by fibroblasts from patients with either Morquio B disease or infantile GM1-gangliosidosis is linked to deficiency in the 67-kD spliced variant of beta-galactosidase. Am J Hum Genet. 2000;67:23-36 pubmed
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Zhang S, Bagshaw R, Hilson W, Oho Y, Hinek A, Clarke J, et al. Characterization of beta-galactosidase mutations Asp332-->Asn and Arg148-->Ser, and a polymorphism, Ser532-->Gly, in a case of GM1 gangliosidosis. Biochem J. 2000;348 Pt 3:621-32 pubmed
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Morrone A, Bardelli T, Donati M, Giorgi M, Di Rocco M, Gatti R, et al. beta-galactosidase gene mutations affecting the lysosomal enzyme and the elastin-binding protein in GM1-gangliosidosis patients with cardiac involvement. Hum Mutat. 2000;15:354-66 pubmed
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Callahan J. Molecular basis of GM1 gangliosidosis and Morquio disease, type B. Structure-function studies of lysosomal beta-galactosidase and the non-lysosomal beta-galactosidase-like protein. Biochim Biophys Acta. 1999;1455:85-103 pubmed
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Silva C, Severini M, Sopelsa A, Coelho J, Zaha A, d Azzo A, et al. Six novel beta-galactosidase gene mutations in Brazilian patients with GM1-gangliosidosis. Hum Mutat. 1999;13:401-9 pubmed
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Juers D, Huber R, Matthews B. Structural comparisons of TIM barrel proteins suggest functional and evolutionary relationships between beta-galactosidase and other glycohydrolases. Protein Sci. 1999;8:122-36 pubmed
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Privitera S, Prody C, Callahan J, Hinek A. The 67-kDa enzymatically inactive alternatively spliced variant of beta-galactosidase is identical to the elastin/laminin-binding protein. J Biol Chem. 1998;273:6319-26 pubmed
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Suzuki Y, Yoshitomo Nakagawa K, Maruyama K, Suyama A, Sugano S. Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. Gene. 1997;200:149-56 pubmed
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Kaye E, Shalish C, Livermore J, Taylor H, Stevenson R, Breakefield X. beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosis. J Child Neurol. 1997;12:242-7 pubmed
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Hinek A. Biological roles of the non-integrin elastin/laminin receptor. Biol Chem. 1996;377:471-80 pubmed
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Hinek A, Rabinovitch M, Keeley F, Okamura Oho Y, Callahan J. The 67-kD elastin/laminin-binding protein is related to an enzymatically inactive, alternatively spliced form of beta-galactosidase. J Clin Invest. 1993;91:1198-205 pubmed
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Boustany R, Qian W, Suzuki K. Mutations in acid beta-galactosidase cause GM1-gangliosidosis in American patients. Am J Hum Genet. 1993;53:881-8 pubmed
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Chakraborty S, Rafi M, Wenger D. Mutations in the lysosomal beta-galactosidase gene that cause the adult form of GM1 gangliosidosis. Am J Hum Genet. 1994;54:1004-13 pubmed
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Maruyama K, Sugano S. Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. Gene. 1994;138:171-4 pubmed
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Ishii N, Oohira T, Oshima A, Sakuraba H, Endo F, Matsuda I, et al. Clinical and molecular analysis of a Japanese boy with Morquio B disease. Clin Genet. 1995;48:103-8 pubmed
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Asp N, Dahlqvist A, Koldovsky O. Human small-intestinal beta-galactosidases. Separation and characterization of one lactase and one hetero beta-galactosidase. Biochem J. 1969;114:351-9 pubmed
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Blakely J, MacKenzie S. Purification and properties of a beta-hexosidase from Sporobolomyces singularis. Can J Biochem. 1969;47:1021-5 pubmed
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Oshima A, Tsuji A, Nagao Y, Sakuraba H, Suzuki Y. Cloning, sequencing, and expression of cDNA for human beta-galactosidase. Biochem Biophys Res Commun. 1988;157:238-44 pubmed
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Morreau H, Galjart N, Gillemans N, Willemsen R, van der Horst G, d Azzo A. Alternative splicing of beta-galactosidase mRNA generates the classic lysosomal enzyme and a beta-galactosidase-related protein. J Biol Chem. 1989;264:20655-63 pubmed
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Yamamoto Y, Hake C, Martin B, Kretz K, Ahern Rindell A, Naylor S, et al. Isolation, characterization, and mapping of a human acid beta-galactosidase cDNA. DNA Cell Biol. 1990;9:119-27 pubmed
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Oshima A, Yoshida K, Shimmoto M, Fukuhara Y, Sakuraba H, Suzuki Y. Human beta-galactosidase gene mutations in morquio B disease. Am J Hum Genet. 1991;49:1091-3 pubmed
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Nishimoto J, Nanba E, Inui K, Okada S, Suzuki K. GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients. Am J Hum Genet. 1991;49:566-74 pubmed
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Yoshida K, Oshima A, Shimmoto M, Fukuhara Y, Sakuraba H, Yanagisawa N, et al. Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases. Am J Hum Genet. 1991;49:435-42 pubmed
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Mosna G, Fattore S, Tubiello G, Brocca S, Trubia M, Gianazza E, et al. A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patient. Hum Genet. 1992;90:247-50 pubmed
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product information
Catalog Number :
G3153
Product Name :
β-Galactosidase from Escherichia coli
Product Type :
PROTEINS & ENZYMES
Product Group :
Protein & Pathway Technologies
Product Description :
lyophilized powder, ?500 units/mg protein
company information

MilliporeSigma
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