4\\\'-Acetylbiphenyl-3-carbons\u00E4ure
Artikel-Nr:
(ABCRS93-3703.0010)
Lieferant:
ABCR
Hersteller-Artikelnummer::
S93-3703.0010
Lokale Artikelnummer::
ABCRS93-3703.0010
Beschreibung:
Rubidiumcarbonat ≥99% (Rb-Basis)
VE:
1 * 10 g
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Artikel-Nr:
(BOSSBS-11813R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11813R-CY3
Lokale Artikelnummer::
BOSSBS-11813R-CY3
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
Artikel-Nr:
(HONE13904.9025)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
13904.9025
Lokale Artikelnummer::
HONE13904.9025
Beschreibung:
Strontiumcarbonat
VE:
1 * 25 kg
Lieferant:
Thermo Scientific
Beschreibung:
Magnesium carbonate hydroxide pentahydrate (40,0 - 45,0% MgO) für die Biochemie
Lieferant:
VWR Collection
Beschreibung:
<B>PTFE</B>-ummantelter Kern aus seltenen Erden. Der magnetische Kern besteht aus einer Kombination aus Samarium und Kobalt. Die Rührer werden für viele Jahre bei voller Stärke funktionieren, da der Magnetismus länger erhalten bleibt. Zu erkennen an dem karbonschwarzem Punkt.
Lieferant:
Biotium
Beschreibung:
Recognizes a glycoprotein of ~200 kDa, identified as carbonic anhydrase IX (CAIX/gp200). Its epitope resides in the carbohydrate domain of gp200. It shows no significant cross-reactivity with other carbohydrate determinants, such as the Lewis blood group antigens, epithelial membrane antigen, HMFG, and AB blood group antigens. In normal kidney, gp200 is localized along the brush border of the pars convoluta and pars recta segments of the proximal tubule, as well as focally along the luminal surface of Bowman's capsule adjoining the outgoing proximal tubule. Reportedly, gp200 is expressed by 93% of primary and 84% of metastatic renal cell carcinomas. This MAb may be useful in the investigations of carcinomas of proximal nephrogenic differentiation especially those showing tubular differentiation.
Lieferant:
Biotium
Beschreibung:
Recognizes a glycoprotein of ~200 kDa, identified as carbonic anhydrase IX (CAIX/gp200). Its epitope resides in the carbohydrate domain of gp200. It shows no significant cross-reactivity with other carbohydrate determinants, such as the Lewis blood group antigens, epithelial membrane antigen, HMFG, and AB blood group antigens. In normal kidney, gp200 is localized along the brush border of the pars convoluta and pars recta segments of the proximal tubule, as well as focally along the luminal surface of Bowman's capsule adjoining the outgoing proximal tubule. Reportedly, gp200 is expressed by 93% of primary and 84% of metastatic renal cell carcinomas. This MAb may be useful in the investigations of carcinomas of proximal nephrogenic differentiation especially those showing tubular differentiation.
Lieferant:
Biotium
Beschreibung:
Recognizes a glycoprotein of ~200 kDa, identified as carbonic anhydrase IX (CAIX/gp200). Its epitope resides in the carbohydrate domain of gp200. It shows no significant cross-reactivity with other carbohydrate determinants, such as the Lewis blood group antigens, epithelial membrane antigen, HMFG, and AB blood group antigens. In normal kidney, gp200 is localized along the brush border of the pars convoluta and pars recta segments of the proximal tubule, as well as focally along the luminal surface of Bowman's capsule adjoining the outgoing proximal tubule. Reportedly, gp200 is expressed by 93% of primary and 84% of metastatic renal cell carcinomas. This MAb may be useful in the investigations of carcinomas of proximal nephrogenic differentiation especially those showing tubular differentiation.
Artikel-Nr:
(BOSSBS-11813R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11813R-A555
Lokale Artikelnummer::
BOSSBS-11813R-A555
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
Artikel-Nr:
(BOSSBS-11813R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11813R-A350
Lokale Artikelnummer::
BOSSBS-11813R-A350
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:
VARIAN
Beschreibung:
Bondesil Carbon 10 g
Artikel-Nr:
(YSIL1579)
Lieferant:
YSI LIFE SCIENCE
Hersteller-Artikelnummer::
1579
Lokale Artikelnummer::
YSIL1579
Beschreibung:
Carbonate buffer concentrate for use with methanol membranes and ethanol membranes. Reconstitute to make 1 litre.
VE:
1 * 1 L
Artikel-Nr:
(BOSSBS-11822R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-CY3
Lokale Artikelnummer::
BOSSBS-11822R-CY3
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:
VWR Collection
Beschreibung:
<B>424: </B>Für die Filtration von Blei-, Eisen- und Silbersulfid, Alkalicarbonat, Bleichromat, Arsen, Antimon, Cadmium und Lebensmitteln. Bestimmung des Sandgehalts in Milchprodukten. Bestimmung der Weiße in Papier und Zellstoff (Papierfabrik).
Artikel-Nr:
(BOSSBS-11822R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A350
Lokale Artikelnummer::
BOSSBS-11822R-A350
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:
Molekula
Beschreibung:
Cäsiumcarbonat
Preis auf Anfrage
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