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Procurou por: N-Fmoc-N-benzyl-glycine


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Fornecedor: Avantor
Descrição: Glicina ≥99.5% (dried basis), ultra puro Bioreagent for Electrophoresis, Liquid Chromatography and Molecular Biology, for liquid chromatography, J.T.Baker®
Código de Artigo: (87973.180)
Fornecedor: VWR Chemicals
Descrição: Ácido 4-Amino-Hipúrico Reag. Ph. Eur. 1003701
UOM: 1 * 100 mL

MSDS Certificados


Fornecedor: VWR Chemicals
Descrição: Biological buffers are useful for cell culture <i>in vitro</i>, enzyme assays and some electrophoretic applications at physiological pH.
Fornecedor: Avantor
Descrição: Glicina 98.5-101.5% USP, Multi-compendial, J.T.Baker®
Código de Artigo: (ABCAAB97628-50)
Fornecedor: Abcam
Descrição: Anti-alpha 2 Glycine Receptor Rabbit Polyclonal Antibody
UOM: 1 * 50 µl


Código de Artigo: (USBIG8167-02)
Fornecedor: US Biological
Descrição: Anti-Glycine Receptor alpha 1/2 Rabbit polyclonal antibody
UOM: 1 * 200 µG


Código de Artigo: (84202.601)
Fornecedor: VWR Chemicals
Descrição: Kit para análise ambiental, Comprimidos de glicina, VWR®
UOM: 1 * 1 UN

MSDS Certificados


Código de Artigo: (USBIG8167-03A)
Fornecedor: US Biological
Descrição: Anti-Glycine Receptor alpha 3 subunit Rabbit polyclonal antibody
UOM: 1 * 100 µG


Código de Artigo: (ABCAAB9442-500)
Fornecedor: Abcam
Descrição: Anti-Glycine Rabbit Polyclonal Antibody
UOM: 1 * 500 µl


Código de Artigo: (BOSSBS-13370R)
Fornecedor: Bioss
Descrição: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-13370R-A488)
Fornecedor: Bioss
Descrição: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-13370R-CY3)
Fornecedor: Bioss
Descrição: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-13370R-FITC)
Fornecedor: Bioss
Descrição: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
UOM: 1 * 100 µl


Código de Artigo: (1.09432.1000)
Fornecedor: Merck
Descrição: Materiais para a calibração exacta e a monitorização de medidores de pH.
UOM: 1 * 1 L

MSDS Certificados


Código de Artigo: (USBIG8167-03)
Fornecedor: US Biological
Descrição: Anti-Glycine Receptor Subunit alpha 1 Mouse monoclonal antibody [clone: 9G364]
UOM: 1 * 100 µG


Fornecedor: SIGMA ALDRICH MICROSCOPY
Descrição: Benzophenone imine plays a vital role as an ammonia surrogate. It is primarily used as ammonia equivalents for the selective formation of protected primary amines. Benzophenone imine is useful as a synthetic intermediate, especially for the synthesis of glycine Schiff base. Benzophenone imine is useful for the preparation of nitrile yield dimers.

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O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call ainda é exibida e precisar de ajuda, por favor, ligue para 213 600 770
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call está visível e precisar de ajuda, por favor, ligue para 213 600 770
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão.
Este produto está bloqueado. Para obter mais informações, contacte a VWR através do número 213 600 770.
O produto pretendido já não se encontra disponível. O produto indicado é um substituto.
Este produto encontra-se em rutura de stock. Poderá encontrar alternativas pesquisando pelo código de artigo indicado acima. Se precisar de ajuda, por favor contacte a VWR através do 213 600 770.
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