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PHARMABLOCK
Artikel-Nr:
(BOSSBS-3953R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3953R-A555
Lokale Artikelnummer::
BOSSBS-3953R-A555
Beschreibung:
Cytochrome c oxidase subunit I (COI or MTCO1) is one of three mitochondrial DNA (mtDNA) encoded subunits (MTCO1, MTCO2, MTCO3) of respiratory Complex IV. Complex IV is located within the mitochondrial inner membrane and is the third and final enzyme of the electron transport chain of mitochondrial oxidative phosphorylation. Complex IV is composed of 13 polypeptides. Subunits I, II, and III (MTCO1, MTCO2, MTCO3) are encoded by mtDNA while subunits IV, Va, Vb, VIa, VIb, VIc, VIIa, VIIb, VIIc, and VIII are nuclear encoded. Mammalian MTCO1 has 12 membrane-spanning alpha-helices (I to XII).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5045R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5045R-A680
Lokale Artikelnummer::
BOSSBS-5045R-A680
Beschreibung:
The protein encoded by this gene, a member of the carnitine/choline acetyltransferase family, is the rate-controlling enzyme of the long-chain fatty acid beta-oxidation pathway in muscle mitochondria. This enzyme is required for the net transport of long-chain fatty acyl-CoAs from the cytoplasm into the mitochondria. Multiple transcript variants encoding different isoforms have been found for this gene, and read-through transcripts are expressed from the upstream locus that include exons from this gene.
VE:
1 * 100 µl
Artikel-Nr:
(CHMP003020.0025)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
003020.0025
Lokale Artikelnummer::
CHMP003020.0025
Beschreibung:
Erbium(III)oxid
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-13312R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13312R-A350
Lokale Artikelnummer::
BOSSBS-13312R-A350
Beschreibung:
GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13312R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13312R-A555
Lokale Artikelnummer::
BOSSBS-13312R-A555
Beschreibung:
GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13312R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13312R-CY7
Lokale Artikelnummer::
BOSSBS-13312R-CY7
Beschreibung:
GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1859R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1859R-A488
Lokale Artikelnummer::
BOSSBS-1859R-A488
Beschreibung:
Involved in oxygen transport in the brain. Hexacoordinate globin, displaying competitive binding of oxygen or the distal His residue to the iron atom. Not capable of penetrating cell membranes. The deoxygenated form exhibits nitrite reductase activity inhibiting cellular respiration via NO-binding to cytochrome c oxidase. Involved in neuroprotection during oxidative stress. May exert its anti-apoptotic activity by acting to reset the trigger level of mitochondrial cytochrome c release necessary to commit the cells to apoptosis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3831R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3831R-A647
Lokale Artikelnummer::
BOSSBS-3831R-A647
Beschreibung:
Catalyzes the initial step in triglyceride hydrolysis in adipocyte and non-adipocyte lipid droplets. Also has acylglycerol transacylase activity. May act coordinately with LIPE/HLS within the lipolytic cascade. Regulates adiposome size and may be involved in the degradation of adiposomes. May play an important role in energy homeostasis. May play a role in the response of the organism to starvation, enhancing hydrolysis of triglycerides and providing free fatty acids to other tissues to be oxidized in situations of energy depletion.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1859R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1859R-HRP
Lokale Artikelnummer::
BOSSBS-1859R-HRP
Beschreibung:
Involved in oxygen transport in the brain. Hexacoordinate globin, displaying competitive binding of oxygen or the distal His residue to the iron atom. Not capable of penetrating cell membranes. The deoxygenated form exhibits nitrite reductase activity inhibiting cellular respiration via NO-binding to cytochrome c oxidase. Involved in neuroprotection during oxidative stress. May exert its anti-apoptotic activity by acting to reset the trigger level of mitochondrial cytochrome c release necessary to commit the cells to apoptosis.
VE:
1 * 100 µl
Artikel-Nr:
(MOLE49280974-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
49280974-500G
Lokale Artikelnummer::
MOLE49280974-500G
Beschreibung:
Bismut(III)oxid
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(CHMP006920-100G)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
006920-100G
Lokale Artikelnummer::
CHMP006920-100G
Beschreibung:
Samarium(III)oxid
VE:
1 * 100 g
Artikel-Nr:
(BOSSBS-5045R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5045R-A647
Lokale Artikelnummer::
BOSSBS-5045R-A647
Beschreibung:
The protein encoded by this gene, a member of the carnitine/choline acetyltransferase family, is the rate-controlling enzyme of the long-chain fatty acid beta-oxidation pathway in muscle mitochondria. This enzyme is required for the net transport of long-chain fatty acyl-CoAs from the cytoplasm into the mitochondria. Multiple transcript variants encoding different isoforms have been found for this gene, and read-through transcripts are expressed from the upstream locus that include exons from this gene. [provided by RefSeq, Jun 2009].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2589R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2589R-A555
Lokale Artikelnummer::
BOSSBS-2589R-A555
Beschreibung:
Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Most active in catalyzing 2-hydroxylation. Caffeine is metabolized primarily by cytochrome CYP1A2 in the liver through an initial N3-demethylation. Also acts in the metabolism of aflatoxin B1 and acetaminophen. Participates in the bioactivation of carcinogenic aromatic and heterocyclic amines. Catalizes the N-hydroxylation of heterocyclic amines and the O-deethylation of phenacetin.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2589R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2589R-CY3
Lokale Artikelnummer::
BOSSBS-2589R-CY3
Beschreibung:
Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Most active in catalyzing 2-hydroxylation. Caffeine is metabolized primarily by cytochrome CYP1A2 in the liver through an initial N3-demethylation. Also acts in the metabolism of aflatoxin B1 and acetaminophen. Participates in the bioactivation of carcinogenic aromatic and heterocyclic amines. Catalizes the N-hydroxylation of heterocyclic amines and the O-deethylation of phenacetin.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7693R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7693R-HRP
Lokale Artikelnummer::
BOSSBS-7693R-HRP
Beschreibung:
Catalyzes the oxidation of the less abundant alpha-NAD(P)H isoform to form beta-NAD(P)(+). The enzyme hormone is secreted by the kidney, and circulates in blood and modulates cardiac function and systemic blood pressure. Lowers blood pressure in vivo by decreasing cardiac contractility and heart rate and preventing a compensatory increase in peripheral vascular tone, suggesting a causal link to the increased plasma catecholamine and heightened cardiovascular risk. High concentrations of catecholamines activate plasma renalase and promotes its secretion and synthesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12868R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12868R-CY5
Lokale Artikelnummer::
BOSSBS-12868R-CY5
Beschreibung:
In human liver cytosolic fractions, four forms of biliverdin reductase have been identified, including two biliverdin-IX Beta reductases and two biliverdin-IX Alpha reductases, designated isozymes I and II and isozymes III and IV, respectively. Biliverdin reductase A (BLVRA), also designated biliverdin-IX Alpha-reductase, belongs to the GFO/iIDH/MocA family and the biliverdin reductase subfamily. The gene that encodes this cytoplasmic protein maps to chromosome 7p14-cen. BLVRA reduces biliverdin IX ?(the ?methene bridge of the open tetrapyrrole) to bilirubin with the concomitant oxidation of an NADH or NADPH cofactor (bilirubin + NADP+ = biliverdin + NADPH). BLVRA is expressed primarily in liver.
VE:
1 * 100 µl
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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