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Colecalciferol+(Vitamin+D3)
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Colecalciferol+(Vitamin+D3)
Artikel-Nr:
(BOSSBS-10486R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10486R-A488
Lokale Artikelnummer::
BOSSBS-10486R-A488
Beschreibung:
This gene encodes a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form by the thrombin-thrombomodulin complex. This activated form contains a serine protease domain and functions in degradation of the activated forms of coagulation factors V and VIII. Mutations in this gene have been associated with thrombophilia due to protein C deficiency, neonatal purpura fulminans, and recurrent venous thrombosis.[provided by RefSeq, Dec 2009].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0062R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0062R-A488
Lokale Artikelnummer::
BOSSBS-0062R-A488
Beschreibung:
Calretinin is a calcium-binding protein which is abundant in auditory neurons. It belongs to the calbindin family. Calbindin 2 (calretinin), closely related to calbindin 1, is an intracellular calcium-binding protein belonging to the troponin C superfamily. Calbindin 1 is known to be involved in the vitamin-D-dependent calcium absorption through intestinal and renal epithelia, while the function of neuronal calbindin 1 and calbindin2 is poorly understood. The sequence of the calbindin 2 cDNA reveals an open reading frame of 271 codons coding for a protein of 31,520 Da, and shares 58% identical residues with human calbindin1.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0062R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0062R-A680
Lokale Artikelnummer::
BOSSBS-0062R-A680
Beschreibung:
Calretinin is a calcium-binding protein which is abundant in auditory neurons. It belongs to the calbindin family. Calbindin 2 (calretinin), closely related to calbindin 1, is an intracellular calcium-binding protein belonging to the troponin C superfamily. Calbindin 1 is known to be involved in the vitamin-D-dependent calcium absorption through intestinal and renal epithelia, while the function of neuronal calbindin 1 and calbindin2 is poorly understood. The sequence of the calbindin 2 cDNA reveals an open reading frame of 271 codons coding for a protein of 31520 Da, and shares 58% identical residues with human calbindin1.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9595R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9595R
Lokale Artikelnummer::
BOSSBS-9595R
Beschreibung:
Folate is an essential vitamin that must be obtained from food intake through intestinal absorption in mammals. Folate and reduced folic acid derivatives bind to the folate receptor (FR) family, which mediates the endocytosis of 5-methyltetrahydofolate into the cell.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10486R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10486R-FITC
Lokale Artikelnummer::
BOSSBS-10486R-FITC
Beschreibung:
This gene encodes a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form by the thrombin-thrombomodulin complex. This activated form contains a serine protease domain and functions in degradation of the activated forms of coagulation factors V and VIII. Mutations in this gene have been associated with thrombophilia due to protein C deficiency, neonatal purpura fulminans, and recurrent venous thrombosis.[provided by RefSeq, Dec 2009].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9973R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9973R-A750
Lokale Artikelnummer::
BOSSBS-9973R-A750
Beschreibung:
Leber congenital amaurosis (LCA) is one of the most common causes of hereditary blindness or severe visual impairment in infants. Mutations in several genes with diverse functions mapping to two loci have been implicated in LCA causation. These proteins are involved in processes such as photoreceptor development and maintenance, phototransduction, vitamin A metabolism and protein trafficking. LCA5, also known as Lebercilin, is a ciliary protein that is widely expressed during development and localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9512R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9512R-CY7
Lokale Artikelnummer::
BOSSBS-9512R-CY7
Beschreibung:
Protein S (PROS) is a vitamin K-dependent plasma protein that inhibits blood clotting by serving as a cofactor for activated protein C (APC) and facilitates clearance of early apoptotic cells. In the plasma, circulating Protein S becomes inactive upon complexing with C4b-binding protein (C4BP); 60-70% of Protein S circulates in complex with C4BP. Calcium-dependent association of C4BP-Protein S with apoptotic cells influences the regulation of complement activation. Protein S has APC-independent anticoagulant activity through direct inhibition of prothrombin activation via interactions with Factor X A, Factor V A and phospholipids. Autosomal dominant Protein S deficiency (levels 15 to 37% of normal) correlates with severe recurrent venous thrombosis.
VE:
1 * 100 µl
Lieferant:
Cayman Chemical
Beschreibung:
Lutein (Xanthophyll) is a natural yellow carotenoid, which can be found in plants, egg yolks, and in the human retina. It is a lipid-soluble antioxidant that can circulate in the plasma and confer cardioprotective, anti-inflammatory, and anti-angiogenic effects. Dietary lutein, in combination with zeaxanthin, vitamins and ω-3 fatty acids, may be beneficial against age-related macular degeneration and cataract development.
Artikel-Nr:
(BOSSBS-11813R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11813R-A750
Lokale Artikelnummer::
BOSSBS-11813R-A750
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 catalyses 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 characterised 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-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11813R-FITC
Lokale Artikelnummer::
BOSSBS-11813R-FITC
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-6038R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6038R-FITC
Lokale Artikelnummer::
BOSSBS-6038R-FITC
Beschreibung:
A number of specific carrier proteins for members of the vitamin A family have been discovered. Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. The inducibility of the CRABP2 gene suggests that this isoform is important in retinoic acid-mediated regulation of human skin growth and differentiation. It has been postulated that the CRABP2 gene is transcriptionally regulated by a newly synthesized regulatory protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6038R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6038R-A647
Lokale Artikelnummer::
BOSSBS-6038R-A647
Beschreibung:
A number of specific carrier proteins for members of the vitamin A family have been discovered. Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. The inducibility of the CRABP2 gene suggests that this isoform is important in retinoic acid-mediated regulation of human skin growth and differentiation. It has been postulated that the CRABP2 gene is transcriptionally regulated by a newly synthesized regulatory protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6038R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6038R-A488
Lokale Artikelnummer::
BOSSBS-6038R-A488
Beschreibung:
A number of specific carrier proteins for members of the vitamin A family have been discovered. Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. The inducibility of the CRABP2 gene suggests that this isoform is important in retinoic acid-mediated regulation of human skin growth and differentiation. It has been postulated that the CRABP2 gene is transcriptionally regulated by a newly synthesized regulatory protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9513R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9513R-CY7
Lokale Artikelnummer::
BOSSBS-9513R-CY7
Beschreibung:
This gene encodes a liver vitamin K-dependent glycoprotein that is synthesized in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9513R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9513R-CY3
Lokale Artikelnummer::
BOSSBS-9513R-CY3
Beschreibung:
This gene encodes a liver vitamin K-dependent glycoprotein that is synthesized in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9513R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9513R-A750
Lokale Artikelnummer::
BOSSBS-9513R-A750
Beschreibung:
This gene encodes a liver vitamin K-dependent glycoprotein that is synthesised in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants.
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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