Codice catalogo: (BOSSBS-15589R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-15589R-A750

Codice articolo locale: BOSSBS-15589R-A750

Descrizione: OXCT2 is a testis-specific succinyl-CoA:3-oxoacid CoA transferase (EC 2,8,3,5), which catalyses the reversible transfer of CoA from succinyl-CoA to acetoacetate in the first step of ketone body utilisation. See also OXCT1 (MIM 601424).

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-2698R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-2698R-CY5

Codice articolo locale: BOSSBS-2698R-CY5

Descrizione: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-2698R-CY5.5)

Fornitore: Bioss

Codice articolo fornitore: BS-2698R-CY5.5

Codice articolo locale: BOSSBS-2698R-CY5.5

Descrizione: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15472R-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-15472R-A647

Codice articolo locale: BOSSBS-15472R-A647

Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15472R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-15472R-A488

Codice articolo locale: BOSSBS-15472R-A488

Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5041R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-5041R-CY5

Codice articolo locale: BOSSBS-5041R-CY5

Descrizione: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5041R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-5041R-HRP

Codice articolo locale: BOSSBS-5041R-HRP

Descrizione: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-2698R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-2698R-A750

Codice articolo locale: BOSSBS-2698R-A750

Descrizione: Proton-linked monocarboxylate transporter. catalyses the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-2698R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-2698R-HRP

Codice articolo locale: BOSSBS-2698R-HRP

Descrizione: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5041R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-5041R-CY3

Codice articolo locale: BOSSBS-5041R-CY3

Descrizione: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15472R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15472R-A350

Codice articolo locale: BOSSBS-15472R-A350

Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15472R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-15472R-CY5

Codice articolo locale: BOSSBS-15472R-CY5

Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15472R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-15472R-A750

Codice articolo locale: BOSSBS-15472R-A750

Descrizione: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5041R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-5041R-A680

Codice articolo locale: BOSSBS-5041R-A680

Descrizione: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyses the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5041R-CY5.5)

Fornitore: Bioss

Codice articolo fornitore: BS-5041R-CY5.5

Codice articolo locale: BOSSBS-5041R-CY5.5

Descrizione: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5041R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-5041R-A488

Codice articolo locale: BOSSBS-5041R-A488

Descrizione: This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promo