G4256
Galactose-1-phosphate Uridyltransferase from galactose-adapted yeast
Type IV, lyophilized powder, 20-60 units/mg protein (modified Warburg-Christian)
Sinônimo(s):
GALT, UDP glucose:α-D-galactose-1-phosphate uridyltransferase
Faça loginpara ver os preços organizacionais e de contrato
Selecione um tamanho
20 UNITS
R$ 6.739,00
50 UNITS
R$ 14.837,00
R$ 6.739,00
Check Cart for Availability
Os fabricantes de diagnósticos devem usar produtos de grau alternativo: SRE0008
Solicite uma grande encomenda
Selecione um tamanho
Alterar visualização
20 UNITS
R$ 6.739,00
50 UNITS
R$ 14.837,00
About This Item
Número CAS:
Número MDL:
Código UNSPSC:
12352204
NACRES:
NA.54
R$ 6.739,00
Check Cart for Availability
Os fabricantes de diagnósticos devem usar produtos de grau alternativo: SRE0008
Solicite uma grande encomenda
Produtos recomendados
tipo
Type IV
Nível de qualidade
Formulário
lyophilized powder
atividade específica
20-60 units/mg protein (modified Warburg-Christian)
composição
Protein, 15-35%
atividade externa
6-phosphogluconate dehydrogenase ≤0.5%
UDP glucose pyrophosphorylase and galactokinase ≤0.2%
temperatura de armazenamento
−20°C
Procurando produtos similares? Visita Guia de comparação de produtos
Descrição geral
Research area: Cell Signaling
Galactose-1-phosphate uridyltransferase (GALT) is a galactose metabolizing enzyme that facilitates the simultaneous conversion of uridine diphosphoglucose (UDP-glucose) and galactose-1-phosphate (gal-1P) to uridine diphosphogalactose (UDP-galactose) and glucose-1-phosphate. Classic Galactosemia (CG) is an inherited metabolic condition caused by deficiency of GALT activity.[1] GALT gene is mapped to human chromosome 9p13.[2] Deficiency of GALT results in type 1 galactosemia.[1]
Galactose-1-phosphate uridyltransferase (GALT) is a galactose metabolizing enzyme that facilitates the simultaneous conversion of uridine diphosphoglucose (UDP-glucose) and galactose-1-phosphate (gal-1P) to uridine diphosphogalactose (UDP-galactose) and glucose-1-phosphate. Classic Galactosemia (CG) is an inherited metabolic condition caused by deficiency of GALT activity.[1] GALT gene is mapped to human chromosome 9p13.[2] Deficiency of GALT results in type 1 galactosemia.[1]
Aplicação
Galactose-1-phosphate Uridyltransferase from galactose-adapted yeast has been used to perform enzyme assays.
Definição da unidade
One unit will form 1.0 μmole of glucose 1-phosphate from UDP-glucose, galactose 1-phosphate and NADP+ per min at pH 8.7 at 25 °C as detected by a coupled system using phosphoglucomutase.
forma física
Contains buffer salts as citrate and reduced glutathione
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
Escolha uma das versões mais recentes:
Certificados de análise (COA)
Lot/Batch Number
Não está vendo a versão correta?
Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.
Já possui este produto?
Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Os clientes também visualizaram
E Crushell et al.
Journal of inherited metabolic disease, 32(3), 412-415 (2009-05-07)
Classical galactosaemia is relatively common in Ireland due to a high carrier rate of the Q188R GALT mutation. It is screened for using a bacterial inhibition assay (BIA) for free galactose. A Beutler assay on day one of life is
En route to deoxygenated N-acetyllactosamine analogues employing uridyl and galactosyl transferases.
Daniel Lazarevic et al.
Carbohydrate research, 344(12), 1449-1452 (2009-06-30)
All monodeoxygenated galactoses were treated with galactokinase, and for the 2-, 3-, and 4-deoxy compounds, transformation into the corresponding galactopyranosyl phosphates could be observed. In case of the 2-deoxy derivative, further reaction via UDP-2-deoxy-D-lyxo-hexose (UDP-2-deoxygalactose), which was also obtained chemically
Nir Dai et al.
Plant physiology, 142(1), 294-304 (2006-07-11)
The Cucurbitaceae translocate a significant portion of their photosynthate as raffinose and stachyose, which are galactosyl derivatives of sucrose. These are initially hydrolyzed by alpha-galactosidase to yield free galactose (Gal) and, accordingly, Gal metabolism is an important pathway in Cucurbitaceae
Neonatal screening, clinical features and genetic testing for galactosemia.
Marco Zaffanello et al.
Genetics in medicine : official journal of the American College of Medical Genetics, 7(3), 211-212 (2005-03-19)
Jane Odhiambo Mumma et al.
Molecular genetics and metabolism, 93(2), 160-171 (2007-11-06)
Galactose is metabolized in humans and other species by the three-enzyme Leloir pathway comprised of galactokinase (GALK), galactose 1-P uridylyltransferase (GALT), and UDP-galactose 4'-epimerase (GALE). Impairment of GALT or GALE in humans results in the potentially lethal disorder galactosemia, and
Active Filters
Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.
Entre em contato com a assistência técnica
