Suche >
1,4-Diazabicyclo[2.2.2]octanebis(sulphur+dioxide)adduct
Drucken
Sie suchten nach:
5 823 results were found
1,4-Diazabicyclo[2.2.2]octanebis(sulphur+dioxide)adduct
Lieferant:
Honeywell Chemicals
Beschreibung:
Bariumcarbonat ≥99%, Puriss. p.a. ACS, Fluka™
Artikel-Nr:
(BOSSBS-6988R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6988R-HRP
Lokale Artikelnummer::
BOSSBS-6988R-HRP
Beschreibung:
RuBisCO catalyzes two reactions: the carboxylation of D-ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate in the photorespiration process. Both reactions occur simultaneously and in competition at the same active site.Sequence similarities: Belongs to the RuBisCO large chain family. Type I subfamily.Post-translational modifications: The disulfide bond which can form between Cys-247 in the large chain dimeric partners within the hexadecamer appears to be associated with oxidative stress and protein turnover (By similarity). The disulfide bonds reported in 1RBO may be the result of oxidation during crystallization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11822R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A680
Lokale Artikelnummer::
BOSSBS-11822R-A680
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyses the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6988R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6988R-CY7
Lokale Artikelnummer::
BOSSBS-6988R-CY7
Beschreibung:
RuBisCO catalyzes two reactions: the carboxylation of D-ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate in the photorespiration process. Both reactions occur simultaneously and in competition at the same active site.Sequence similarities: Belongs to the RuBisCO large chain family. Type I subfamily.Post-translational modifications: The disulfide bond which can form between Cys-247 in the large chain dimeric partners within the hexadecamer appears to be associated with oxidative stress and protein turnover (By similarity). The disulfide bonds reported in 1RBO may be the result of oxidation during crystallization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11822R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-FITC
Lokale Artikelnummer::
BOSSBS-11822R-FITC
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11822R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-HRP
Lokale Artikelnummer::
BOSSBS-11822R-HRP
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Lithiumcarbonat, Sigma-Aldrich®
Artikel-Nr:
(HONE11480.9050)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
11480.9050
Lokale Artikelnummer::
HONE11480.9050
Beschreibung:
Bariumcarbonat
VE:
1 * 50 kg
Lieferant:
SORVALL
Beschreibung:
BIOFlex™ HC Swinging-Bucket Rotor Process more than 35 tube styles from microtubes to 1L bottles, plus conical tubes, microplates, tissue culture flasks and blood bags with the Thermo Scientific™ BIOFlex™ HC Swinging-Bucket Rotor. Innovations such as Auto-Lock rotor exchange, Auto-ID instant rotor identification and speed handles on each rotor lid shorten run set-up time while providing peace of mind that the rotor is secure.
Artikel-Nr:
(BOSSBS-11706R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11706R
Lokale Artikelnummer::
BOSSBS-11706R
Beschreibung:
The aldo-keto reductase 7 (AKR7) family includes AKR7A2, AKR7A3 and AKR7A4 in human, AKR7A5 in mouse and AKR7A2 in rat, all of which function in the metabolism of aflatoxin B(1) and other dicarbonyl-containing compounds. More specifically, AKR7A proteins are involved in the metabolism of compounds with ketone groups on adjacent carbon atoms in a broad range of tissues, notably the liver. The human AKR7A2 gene maps to human chromosome 1p35-36, a region frequently deleted in sporadic colorectal cancer. The functional significance of this correlation lies in the constitutive expression of AKR7A2 in human liver to eliminate aflatoxin (an environmental carcinogen), thus acting as an endogenous chemo-preventative agent.
VE:
1 * 100 µl
Artikel-Nr:
(ABCRAB114616.0100)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB114616.0100
Lokale Artikelnummer::
ABCRAB114616.0100
Beschreibung:
Cäsiumcarbonat
VE:
1 * 100 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
Rubidiumcarbonat, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-7984R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7984R-A350
Lokale Artikelnummer::
BOSSBS-7984R-A350
Beschreibung:
Carbonic anhydrases are a large family of zincmetalloenzymes that catalyze the reversible hydration of carbondioxide. They participate in a variety of biological processes,including respiration, calcification, acid-base balance, boneresorption, and the formation of aqueous humor, cerebrospinalfluid, saliva, and gastric acid. They show extensive diversity intissue distribution and in their subcellular localization. Thecytosolic protein encoded by this gene is predominantly expressedin the salivary glands. Alternative splicing in the coding regionresults in multiple transcript variants encoding differentisoforms. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(PROONIST-987)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
NIST-987
Lokale Artikelnummer::
PROONIST-987
Beschreibung:
Strontiumcarbonat
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11813R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11813R-CY5
Lokale Artikelnummer::
BOSSBS-11813R-CY5
Beschreibung:
Biotin, also known as vitamin B7, is an essential water-soluble vitamin that is a cofactor in glucogenesis and in the metabolism of fatty acids and leucine. Biotinidase is a 523 amino acid enzyme that catalyzes the hydrolysis of biocytin to biotin and lysine. Secreted into extracellular space, biotinidase is expressed in liver, heart, placenta, brain, skeletal muscle, pancreas and kidney. Biotinidase contains one carbon-nitrogen hydrolase domain, which is involved in the reduction of organic nitrogen compounds and ammonia production. Defects in the gene encoding biotinidase are the cause of biotinidase deficiency, which is characterized by skin rash, ataxia, seizures, hearing loss, hypotonia and optic atrophy. These symptoms are due to the individual’s inability to reutilize biotin and can, therefore, typically be treated with the addition of free biotin.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Strontiumcarbonat, Sigma-Aldrich®
Preis auf Anfrage
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.
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
