Procurou por: Luzes+de+Halog\u00E9neo

Descrição: Diethyl ethylmalonate, Sigma-Aldrich®

Código de Artigo: 8.00906.0250

UOM: 1 * 250 mL

Fornecedor: Merck

MSDS Promoção

Descrição: Diethyl ethylmalonate ≥98.0% (by GC)

Código de Artigo: TCIAE0138-500ML

UOM: 1 * 500 mL

Fornecedor: TCI

Promoção

Descrição: Diethyl ethylmalonate 99%

Código de Artigo: ACRO114365000

UOM: 1 * 500 g

Fornecedor: Thermo Fisher Scientific

MSDS Promoção

Descrição: Diethyl ethylmalonate, Sigma-Aldrich®

Código de Artigo: SIALD95204-100G

UOM: 1 * 100 g

Fornecedor: Merck

Promoção

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

Código de Artigo: TCIAE0137-25G

UOM: 1 * 25 g

Fornecedor: TCI

Promoção

Descrição: Ethylmalonic acid ≥97%

Código de Artigo: B20715.22

UOM: 1 * 100 g

Fornecedor: Thermo Fisher Scientific

MSDS Certificados Promoção

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.

Código de Artigo: BOSSBS-7610R-A555

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-A647

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-HRP

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-A350

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-A488

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-CY3

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-A680

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-7610R-A750

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: Dimethyl ethylmalonate, Sigma-Aldrich®

Código de Artigo: SIAL04285-100ML

UOM: 1 * 100 mL

Fornecedor: Merck

Promoção