Sie suchten nach: Methylsuccinic+anhydride

Lieferant: Apollo Scientific

Beschreibung: Methylsuccinic anhydride 98%

Lieferant: Thermo Scientific

Beschreibung: Methylsuccinic anhydride 97%

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Lieferant: Apollo Scientific

Beschreibung: Methylsuccinic acid 95%

Lieferant: Apollo Scientific

Beschreibung: (S)-(-)-Methylsuccinic acid 95%

Artikel-Nr: (APOSOR953141-1G)

Lieferant: Apollo Scientific

Beschreibung: Dimethyl (R)-(+)-methylsuccinate 97%

VE: 1 * 1 g

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Lieferant: Apollo Scientific

Beschreibung: (R)-(+)-Methylsuccinic acid 95%

Artikel-Nr: (APOSOR913785-1G)

Lieferant: Apollo Scientific

Beschreibung: Dimethyl (S)-(-)-methylsuccinate 95%

VE: 1 * 1 g

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Lieferant: Apollo Scientific

Beschreibung: Dimethyl methylsuccinate 95%

Artikel-Nr: (BOSSBS-7610R-CY5.5)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7610R-CY5)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7610R-CY7)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-7610R-FITC)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-7610R-A750)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-7610R)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-7610R-A555)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-7610R-CY3)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!