You Searched For: Primaquine+diphosphate

Catalog Number: (BOSSBS-5073R-CY5)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-A488)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-A647)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-A680)

Supplier: Bioss

Description: IDI1 is a peroxisomally localised enzyme that catalyses 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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Catalog Number: (ABCAAB162263-10)

Supplier: Abcam

Description: RECOMBINANT HUMAN NUCLEOSIDE DIPHOSPHATE 1 * 10 µG

UOM: 1 * 10 µG

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Catalog Number: (BOSSBS-5073R)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-CY3)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-CY7)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-A350)

Supplier: Bioss

Description: 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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Catalog Number: (CAYM22982-5)

Supplier: Cayman Chemical

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

UOM: 1 * 5 mg

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Catalog Number: (APOSOR1013448-5G)

Supplier: Apollo Scientific

Description: Guanosine-5-Diphosphate Disodium Salt 5g pack 1 * 5 g

UOM: 1 * 5 g

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Catalog Number: (ABCAAB146529-500)

Supplier: Abcam

Description: GUANOSINE 5'-DIPHOSPHATE [GDP] DISOD 1 * 500 mg

UOM: 1 * 500 mg

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Catalog Number: (ABCAAB146529-100)

Supplier: Abcam

Description: GUANOSINE 5'-DIPHOSPHATE [GDP] DISOD 1 * 100 mg

UOM: 1 * 100 mg

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Catalog Number: (BOSSBS-5073R-A555)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-FITC)

Supplier: Bioss

Description: 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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Catalog Number: (BOSSBS-5073R-A750)

Supplier: Bioss

Description: IDI1 is a peroxisomally localised enzyme that catalyses 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