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Hai cercato: N-Acetyl-L-isoleucine


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Fornitore: Thermo Scientific
Descrizione: N-Acetyl-L-isoleucine 98% (by HPLC)

Fornitore: Apollo Scientific
Descrizione: Acetyl-d-alloisoleucine 95%

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Codice catalogo: (BOSSBS-5019R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-A750
Codice articolo locale: BOSSBS-5019R-A750
Descrizione: This gene encodes a mitochondrially localised enzyme that catalyses the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterised by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-A350
Codice articolo locale: BOSSBS-5019R-A350
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-A555
Codice articolo locale: BOSSBS-5019R-A555
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R
Codice articolo locale: BOSSBS-5019R
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-FITC
Codice articolo locale: BOSSBS-5019R-FITC
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-A680
Codice articolo locale: BOSSBS-5019R-A680
Descrizione: This gene encodes a mitochondrially localised enzyme that catalyses the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterised by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-A647
Codice articolo locale: BOSSBS-5019R-A647
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-CY5.5
Codice articolo locale: BOSSBS-5019R-CY5.5
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-CY7
Codice articolo locale: BOSSBS-5019R-CY7
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-A488
Codice articolo locale: BOSSBS-5019R-A488
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-CY5
Codice articolo locale: BOSSBS-5019R-CY5
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-CY3
Codice articolo locale: BOSSBS-5019R-CY3
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-5019R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-5019R-HRP
Codice articolo locale: BOSSBS-5019R-HRP
Descrizione: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
UOM: 1 * 100 µl


Codice catalogo: (PHR1099-1G)
Fornitore: Merck
Codice articolo fornitore: PHR1099-1G
Codice articolo locale: SUPLPHR1099-1G
Descrizione: Organic Standard, L-Isoleucine
UOM: 1 * 1 g

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