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Procurou por: Diethyl+ethylmalonate


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Image Unavailable-8.00906.0250

Diethyl ethylmalonate, Sigma-Aldrich®

Código de Artigo: (8.00906.0250)
Fornecedor: Merck
Descrição: Diethyl ethylmalonate, Sigma-Aldrich®
UOM: 1 * 250 mL

MSDS


Image Unavailable-TCIAE0138-500ML

Diethyl ethylmalonate ≥98.0% (por GC)

Fornecedor: TCI
Descrição: Diethyl ethylmalonate ≥98.0% (by GC)

Imagem do Produto-ACRO114365000

Diethyl ethylmalonate 99%

Fornecedor: Thermo Fisher Scientific
Descrição: Diethyl ethylmalonate 99%

MSDS

Image Unavailable-SIALD95204-100G

Diethyl ethylmalonate, Sigma-Aldrich®

Código de Artigo: (SIALD95204-100G)
Fornecedor: Merck
Descrição: Diethyl ethylmalonate, Sigma-Aldrich®
UOM: 1 * 100 g
Image Unavailable-TCIAE0137-25G

Ethylmalonic acid ≥98.0% (por análise titulométrica)

Fornecedor: TCI
Descrição: Ethylmalonic acid ≥98.0% (by titrimetric analysis)

Image Unavailable-B20715.22

Ethylmalonic acid ≥97%

Fornecedor: Thermo Fisher Scientific
Descrição: Ethylmalonic acid ≥97%

MSDS Certificados

Image Unavailable-BOSSBS-7610R-A555

Anti-ETHE1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Código de Artigo: (BOSSBS-7610R-A555)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R

Anti-ETHE1 Rabbit Polyclonal Antibody

Código de Artigo: (BOSSBS-7610R)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-A647

Anti-ETHE1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Código de Artigo: (BOSSBS-7610R-A647)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-HRP

Anti-ETHE1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Código de Artigo: (BOSSBS-7610R-HRP)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-A350

Anti-ETHE1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Código de Artigo: (BOSSBS-7610R-A350)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-A488

Anti-ETHE1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Código de Artigo: (BOSSBS-7610R-A488)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-CY3

Anti-ETHE1 Rabbit Polyclonal Antibody (Cy3®)

Código de Artigo: (BOSSBS-7610R-CY3)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localization of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterized by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-A680

Anti-ETHE1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Código de Artigo: (BOSSBS-7610R-A680)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localisation of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterised by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7610R-A750

Anti-ETHE1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Código de Artigo: (BOSSBS-7610R-A750)
Fornecedor: Bioss
Descrição: Probably plays an important role in metabolic homeostasis in mitochondria. May function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. Suppresses p53-induced apoptosis by preventing nuclear localisation of RELA.Involvement in disease:Defects in ETHE1 are a cause of ethylmalonic encephalopathy (EE) . EE is an autosomal recessive disorder characterised by neurodevelopmental delay and regression, recurrent petechiae, acrocyanosis, diarrhea, leading to death in the first decade of life. It is also associated with persistent lactic acidemia and ethylmalonic and methylsuccinic aciduria.
UOM: 1 * 100 µl
Image Unavailable-SIAL04285-100ML

Dimethyl ethylmalonate, Sigma-Aldrich®

Código de Artigo: (SIAL04285-100ML)
Fornecedor: Merck
Descrição: Dimethyl ethylmalonate, Sigma-Aldrich®
UOM: 1 * 100 mL
Preço sob consulta
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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