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Zinc+copper+composite
Artikel-Nr:
(BOSSBS-3694R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3694R-CY5
Lokale Artikelnummer::
BOSSBS-3694R-CY5
Beschreibung:
High density lipoproteins (HDLs) have been proposed to function jointly with lecithin:cholesterol acyltransferase and CETP to facilitate cholesterol transport from tissues to the liver. This mechanism, referred to as reverse cholesterol transport, is physiologically important because it maintains systemic cholesterol levels. CETP is responsible for neutral lipid transfer activity in plasma in numerous species. Since CETP is able to accelerate specifically the exchange of lipid components between pro- and anti-atherogenic lipoprotein fractions, it may be a key determinant of the global atherogenicity of the plasma lipoprotein profile and arises as a possible target in atherosclerosis prevention. CETP has an important role in reverse cholesterol transport and shaping and affecting the composition of plasma lipoproteins. In general elevated levels of CETP have been associated with increased risk of coronary heart disease.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6898R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6898R-CY7
Lokale Artikelnummer::
BOSSBS-6898R-CY7
Beschreibung:
Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Sequence analysis identified three transcript variants that encode different isoforms. Pseudogenes corresponding to this gene are found on chromosomes 5q and 12q. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6898R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6898R-CY3
Lokale Artikelnummer::
BOSSBS-6898R-CY3
Beschreibung:
Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Sequence analysis identified three transcript variants that encode different isoforms. Pseudogenes corresponding to this gene are found on chromosomes 5q and 12q. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3694R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3694R-CY7
Lokale Artikelnummer::
BOSSBS-3694R-CY7
Beschreibung:
High density lipoproteins (HDLs) have been proposed to function jointly with lecithin:cholesterol acyltransferase and CETP to facilitate cholesterol transport from tissues to the liver. This mechanism, referred to as reverse cholesterol transport, is physiologically important because it maintains systemic cholesterol levels. CETP is responsible for neutral lipid transfer activity in plasma in numerous species. Since CETP is able to accelerate specifically the exchange of lipid components between pro- and anti-atherogenic lipoprotein fractions, it may be a key determinant of the global atherogenicity of the plasma lipoprotein profile and arises as a possible target in atherosclerosis prevention. CETP has an important role in reverse cholesterol transport and shaping and affecting the composition of plasma lipoproteins. In general elevated levels of CETP have been associated with increased risk of coronary heart disease.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12705R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12705R-A680
Lokale Artikelnummer::
BOSSBS-12705R-A680
Beschreibung:
Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that does not seem to have a counterpart in prokaryotic and fungal-mitochondrial ribosomes. This gene lies telomeric of and is transcribed in the opposite direction from the forkhead box L2 gene. A pseudogene corresponding to this gene is found on chromosome Xq.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5952R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5952R-CY3
Lokale Artikelnummer::
BOSSBS-5952R-CY3
Beschreibung:
POMT1 (Protein O mannosyl transferase 1) is a multipass membrane protein that is found in the endoplasmic reticulum. POMT1 catalyses the transfer of mannosyl residues to the hydroxyl groups of serine or threonine residues. Enzymatic activity is dependent on co expression of POMT1 with POMT2. Defects in the POMT1 gene are associated with Walker-Warburg syndrome (WWS), a congential muscular dystrophy that is associated with mental retardation and is usually lethal within the first few months of life. Other defects in the POMT1 gene result in limb girdle muscular dystrophy type 2K (LGMD2K), which is associated with mild mental retardation. Studies in Drosophila suggest that mutation of POMT1 alters the efficacy of synaptic transmission and a change in subunit composition of post synaptic glutamate receptors at the neuromuscular junction. Missense mutations in POMT1 have been associated with glioneuronal and glial brain tumours.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5952R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5952R-HRP
Lokale Artikelnummer::
BOSSBS-5952R-HRP
Beschreibung:
POMT1 (Protein O mannosyl transferase 1) is a multipass membrane protein that is found in the endoplasmic reticulum. POMT1 catalyses the transfer of mannosyl residues to the hydroxyl groups of serine or threonine residues. Enzymatic activity is dependent on co expression of POMT1 with POMT2. Defects in the POMT1 gene are associated with Walker-Warburg syndrome (WWS), a congential muscular dystrophy that is associated with mental retardation and is usually lethal within the first few months of life. Other defects in the POMT1 gene result in limb girdle muscular dystrophy type 2K (LGMD2K), which is associated with mild mental retardation. Studies in Drosophila suggest that mutation of POMT1 alters the efficacy of synaptic transmission and a change in subunit composition of post synaptic glutamate receptors at the neuromuscular junction. Missense mutations in POMT1 have been associated with glioneuronal and glial brain tumours.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5952R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5952R-A555
Lokale Artikelnummer::
BOSSBS-5952R-A555
Beschreibung:
POMT1 (Protein O mannosyl transferase 1) is a multipass membrane protein that is found in the endoplasmic reticulum. POMT1 catalyses the transfer of mannosyl residues to the hydroxyl groups of serine or threonine residues. Enzymatic activity is dependent on co expression of POMT1 with POMT2. Defects in the POMT1 gene are associated with Walker-Warburg syndrome (WWS), a congential muscular dystrophy that is associated with mental retardation and is usually lethal within the first few months of life. Other defects in the POMT1 gene result in limb girdle muscular dystrophy type 2K (LGMD2K), which is associated with mild mental retardation. Studies in Drosophila suggest that mutation of POMT1 alters the efficacy of synaptic transmission and a change in subunit composition of post synaptic glutamate receptors at the neuromuscular junction. Missense mutations in POMT1 have been associated with glioneuronal and glial brain tumours.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3694R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3694R-FITC
Lokale Artikelnummer::
BOSSBS-3694R-FITC
Beschreibung:
High density lipoproteins (HDLs) have been proposed to function jointly with lecithin:cholesterol acyltransferase and CETP to facilitate cholesterol transport from tissues to the liver. This mechanism, referred to as reverse cholesterol transport, is physiologically important because it maintains systemic cholesterol levels. CETP is responsible for neutral lipid transfer activity in plasma in numerous species. Since CETP is able to accelerate specifically the exchange of lipid components between pro- and anti-atherogenic lipoprotein fractions, it may be a key determinant of the global atherogenicity of the plasma lipoprotein profile and arises as a possible target in atherosclerosis prevention. CETP has an important role in reverse cholesterol transport and shaping and affecting the composition of plasma lipoproteins. In general elevated levels of CETP have been associated with increased risk of coronary heart disease.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5952R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5952R-A647
Lokale Artikelnummer::
BOSSBS-5952R-A647
Beschreibung:
POMT1 (Protein O mannosyl transferase 1) is a multipass membrane protein that is found in the endoplasmic reticulum. POMT1 catalyses the transfer of mannosyl residues to the hydroxyl groups of serine or threonine residues. Enzymatic activity is dependent on co expression of POMT1 with POMT2. Defects in the POMT1 gene are associated with Walker-Warburg syndrome (WWS), a congential muscular dystrophy that is associated with mental retardation and is usually lethal within the first few months of life. Other defects in the POMT1 gene result in limb girdle muscular dystrophy type 2K (LGMD2K), which is associated with mild mental retardation. Studies in Drosophila suggest that mutation of POMT1 alters the efficacy of synaptic transmission and a change in subunit composition of post synaptic glutamate receptors at the neuromuscular junction. Missense mutations in POMT1 have been associated with glioneuronal and glial brain tumours.
VE:
1 * 100 µl
Artikel-Nr:
(APOSIN1549-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
IN1549-25G
Lokale Artikelnummer::
APOSIN1549-25G
Beschreibung:
Kupfer(2+)bis(dimethylcarbamodithioat) 98%
VE:
1 * 25 g
Artikel-Nr:
(23123.294)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC23123.294
Beschreibung:
Kupfer(II)nitrat Trihydrat ≥98%, GPR RECTAPUR®
VE:
1 * 1 kg
Artikel-Nr:
(APOSIN1531-250G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
IN1531-250G
Lokale Artikelnummer::
APOSIN1531-250G
Beschreibung:
Kupfer 99.999%, Perlen 4 - 6 mm
VE:
1 * 250 g
Lieferant:
Merck
Beschreibung:
Kupfer(II)sulfat Pentahydrat, Supelco®
Artikel-Nr:
(85696.601)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC85696.601
Beschreibung:
Semi-quantitative test strips for the determination of copper.
VE:
1 * 100 ST
Lieferant:
Merck
Beschreibung:
Kupfer(II)oxid ACS analytisches Reagens, Supelco®
Preis auf Anfrage
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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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