Sie suchten nach: Primaquine+diphosphate

Artikel-Nr: (PRSI55-260)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 55-260

Beschreibung: Probably mediates the hydrolysis of some nucleoside diphosphate derivatives (By similarity).

UOM: 1 * 400 µl

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Artikel-Nr: (BOSSBS-8039R)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8039R

Beschreibung: This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important molecule responsible for the C20-prenylation of proteins and for the regulation of a nuclear hormone receptor. Alternate transcriptional splice variants, both protein-coding and non-protein-coding, have been found for this gene. [provided by RefSeq, Sep 2010].

UOM: 1 * 100 µl

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Artikel-Nr: (USBI130429)

Lieferant: US Biological

Hersteller Artikel Nummer : 130429

Beschreibung: Anti-NME5 Mouse Monoclonal Antibody [clone: 4F5]

UOM: 1 * 100 µG

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Artikel-Nr: (CAYM18897-25)

Lieferant: Cayman Chemical

Hersteller Artikel Nummer : 18897-25

Beschreibung: 5-PHOSPHO-D-RIBOSE 1-DIPHOSPHATE (SODIUM 1 * 25 mg

UOM: 1 * 25 mg

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Artikel-Nr: (CAYM18897-10)

Lieferant: Cayman Chemical

Hersteller Artikel Nummer : 18897-10

Beschreibung: 5-PHOSPHO-D-RIBOSE 1-DIPHOSPHATE (SODIUM 1 * 10 mg

UOM: 1 * 10 mg

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Artikel-Nr: (PRSI30-424)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 30-424

Beschreibung: GGPS1 is a member of the prenyltransferase family with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important molecule responsible for the C20-prenylation of proteins and for the regulation of a nuclear hormone receptor.This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important molecule responsible for the C20-prenylation of proteins and for the regulation of a nuclear hormone receptor. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

UOM: 1 * 50 µG

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Artikel-Nr: (ABCAAB162263-10)

Lieferant: Abcam

Hersteller Artikel Nummer : AB162263-10

Beschreibung: RECOMBINANT HUMAN NUCLEOSIDE DIPHOSPHATE 1 * 10 µG

UOM: 1 * 10 µG

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Artikel-Nr: (CAYM22982-5)

Lieferant: Cayman Chemical

Hersteller Artikel Nummer : 22982-5

Beschreibung: 2'-Deoxycytidine 5'-diphosphate (sodium salt hydrate) 1 * 5 mg

UOM: 1 * 5 mg

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Artikel-Nr: (CAYM18897-100)

Lieferant: Cayman Chemical

Hersteller Artikel Nummer : 18897-100

Beschreibung: 5-PHOSPHO-D-RIBOSE 1-DIPHOSPHATE (SODIUM 1 * 100 mg

UOM: 1 * 100 mg

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Artikel-Nr: (ABCAAB105612-500)

Lieferant: Abcam

Hersteller Artikel Nummer : AB105612-500

Beschreibung: RECOMBINANT HUMAN NUCLEOSIDE-DIPHOSPHATE 1 * 500 µG

UOM: 1 * 500 µG

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Artikel-Nr: (BOSSBS-8039R-HRP)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8039R-HRP

Beschreibung: This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important molecule responsible for the C20-prenylation of proteins and for the regulation of a nuclear hormone receptor. Alternate transcriptional splice variants, both protein-coding and non-protein-coding, have been found for this gene. [provided by RefSeq, Sep 2010].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-5073R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-5073R-CY7

Beschreibung: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-5073R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-5073R-A350

Beschreibung: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-5073R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-5073R-CY5

Beschreibung: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-5073R-A488)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-5073R-A488

Beschreibung: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-5073R-A647)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-5073R-A647

Beschreibung: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.

UOM: 1 * 100 µl

Sale