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Procurou por: Medidores+para+adesão


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Descrição: Galactitol ≥98.0% (by GC)
Código de Artigo: TCIAG0005-25G
UOM: 1 * 25 g
Fornecedor: TCI


Descrição: Organic Standard, Galactitol
Código de Artigo: PHR1833-1G
UOM: 1 * 1 g
Fornecedor: Merck


Descrição: Galactitol 99+%
Código de Artigo: ACRO117700250
UOM: 1 * 25 g
Fornecedor: Thermo Fisher Scientific

MSDS


Descrição: 1-Deoxy-D-galactitol 98+%
Código de Artigo: APOSBICL4223-500MG
UOM: 1 * 500 mg
Fornecedor: Apollo Scientific


Descrição: Galactitol ≥97%
Código de Artigo: A18402.36
UOM: 1 * 500 g
Fornecedor: Thermo Fisher Scientific

MSDS Certificados


Descrição: Migalastat hydrochloride
Código de Artigo: APOSOR2365T-10MG
UOM: 1 * 10 mg
Fornecedor: Apollo Scientific


Descrição: Galactitol
Código de Artigo: EDQMG0049000
UOM: 1 * 50 mg
Fornecedor: EDQM


Descrição: Galactitol ≥99%
Código de Artigo: J63206.36
UOM: 1 * 500 g
Fornecedor: Thermo Fisher Scientific

MSDS Certificados


Descrição: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
Código de Artigo: 1287711.
UOM: 1 * 500 mg
Fornecedor: USP


Descrição: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Código de Artigo: BOSSBS-13267R-CY5
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: Galactitol, Sigma-Aldrich®
Código de Artigo: SIALD0256-100G
UOM: 1 * 100 g
Fornecedor: Merck


Descrição: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Código de Artigo: BOSSBS-13267R-CY7
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Código de Artigo: BOSSBS-13267R-FITC
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Código de Artigo: BOSSBS-13267R-CY3
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Código de Artigo: BOSSBS-13267R-HRP
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Código de Artigo: BOSSBS-13267R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss


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