Copper(II)+gluconate
Artikel-Nr:
(41913.GU)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
41913.GU
Lokale Artikelnummer::
ALFA41913.GU
Beschreibung:
Kupfer-Beryllium-Legierung (98,1:1,9 gew.%), Legierung C17200, Folie, Dicke 0.25 mm (0.01 in)
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-8034R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8034R-A680
Lokale Artikelnummer::
BOSSBS-8034R-A680
Beschreibung:
Promotes ubiquitination of NF-kappa-B subunit RELA and its subsequent proteasomal degradation. Down-regulates NF-kappa-B activity. Down-regulates SOD1 activity by interfering with its homodimerisation. Plays a role in copper ion homeostasis. Can bind one copper ion per monomer. May function to facilitate biliary copper excretion within hepatocytes.Tissue specificity:Ubiquitous. Highest expression in the liver, with lower expression in brain, lung, placenta, pancreas, small intestine, heart, skeletal muscle, kidney and placenta.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8034R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8034R-A350
Lokale Artikelnummer::
BOSSBS-8034R-A350
Beschreibung:
Promotes ubiquitination of NF-kappa-B subunit RELA and its subsequent proteasomal degradation. Down-regulates NF-kappa-B activity. Down-regulates SOD1 activity by interfering with its homodimerization. Plays a role in copper ion homeostasis. Can bind one copper ion per monomer. May function to facilitate biliary copper excretion within hepatocytes.Tissue specificity:Ubiquitous. Highest expression in the liver, with lower expression in brain, lung, placenta, pancreas, small intestine, heart, skeletal muscle, kidney and placenta.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8034R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8034R-A555
Lokale Artikelnummer::
BOSSBS-8034R-A555
Beschreibung:
Promotes ubiquitination of NF-kappa-B subunit RELA and its subsequent proteasomal degradation. Down-regulates NF-kappa-B activity. Down-regulates SOD1 activity by interfering with its homodimerization. Plays a role in copper ion homeostasis. Can bind one copper ion per monomer. May function to facilitate biliary copper excretion within hepatocytes.Tissue specificity:Ubiquitous. Highest expression in the liver, with lower expression in brain, lung, placenta, pancreas, small intestine, heart, skeletal muscle, kidney and placenta.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11048R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11048R-FITC
Lokale Artikelnummer::
BOSSBS-11048R-FITC
Beschreibung:
Copper is an essential micronutrient used as a co-factor for several essential enzymes in all living organisms. Due to the high toxicity of copper, its metabolism is tightly regulated and defects in this regulation can cause Menkes (deficiency) or Wilson (accumulation) disease in various tissue. CUTC (cutC copper transporter homolog (E. coli)), also known as CGI-32, is a 273 amino acid protein belonging to the cutC family. CUTC is involved in copper homeostasis and is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11048R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11048R-A350
Lokale Artikelnummer::
BOSSBS-11048R-A350
Beschreibung:
Copper is an essential micronutrient used as a co-factor for several essential enzymes in all living organisms. Due to the high toxicity of copper, its metabolism is tightly regulated and defects in this regulation can cause Menkes (deficiency) or Wilson (accumulation) disease in various tissue. CUTC (cutC copper transporter homolog (E. coli)), also known as CGI-32, is a 273 amino acid protein belonging to the cutC family. CUTC is involved in copper homeostasis and is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11048R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11048R-A680
Lokale Artikelnummer::
BOSSBS-11048R-A680
Beschreibung:
Copper is an essential micronutrient used as a co-factor for several essential enzymes in all living organisms. Due to the high toxicity of copper, its metabolism is tightly regulated and defects in this regulation can cause Menkes (deficiency) or Wilson (accumulation) disease in various tissue. CUTC (cutC copper transporter homolog (E. coli)), also known as CGI-32, is a 273 amino acid protein belonging to the cutC family. CUTC is involved in copper homeostasis and is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides. PTEN is an important tumour suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2617R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2617R-CY5
Lokale Artikelnummer::
BOSSBS-2617R-CY5
Beschreibung:
Plays a role in the export of proteins that lack a signal peptide and are secreted by an alternative pathway. Binds two calcium ions per subunit. Binds one copper ion. Binding of one copper ion does not interfere with calcium binding. Required for the copper-dependent stress-induced export of IL1A and FGF1. The calcium-free protein binds to lipid vesicles containing phosphatidylserine, but not to vesicles containing phosphatidylcholine (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15458R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15458R-CY7
Lokale Artikelnummer::
BOSSBS-15458R-CY7
Beschreibung:
Hephaestin is a single-pass type I membrane protein that belongs to the multicopper oxidase family of proteins. Hephaestin, a copper-dependant ferroxidase protein, is crucial for iron exiting intestinal enterocytes into the circulation. It mediates the movement of iron across the basolateral membrane in conjunction with ferroportin 1. This is an important link between iron and copper metabolism in mammalian systems, as copper deficiency leads to reduced hephaestin and reduced iron absorption resulting in anemia. Hephaestin can bind six copper ions per monomer and is regulated by the homeobox transcription factor CDX2. Increased levels of iron leads to an increase in CDX2 expression and thus Hephaestin. Hephaestin is primarily detected in the intestine, but is also expressed in colon, breast, bone trabecural cells and fibroblasts.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15458R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15458R-A555
Lokale Artikelnummer::
BOSSBS-15458R-A555
Beschreibung:
Hephaestin is a single-pass type I membrane protein that belongs to the multicopper oxidase family of proteins. Hephaestin, a copper-dependant ferroxidase protein, is crucial for iron exiting intestinal enterocytes into the circulation. It mediates the movement of iron across the basolateral membrane in conjunction with ferroportin 1. This is an important link between iron and copper metabolism in mammalian systems, as copper deficiency leads to reduced hephaestin and reduced iron absorption resulting in anemia. Hephaestin can bind six copper ions per monomer and is regulated by the homeobox transcription factor CDX2. Increased levels of iron leads to an increase in CDX2 expression and thus Hephaestin. Hephaestin is primarily detected in the intestine, but is also expressed in colon, breast, bone trabecural cells and fibroblasts.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2617R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2617R-FITC
Lokale Artikelnummer::
BOSSBS-2617R-FITC
Beschreibung:
Plays a role in the export of proteins that lack a signal peptide and are secreted by an alternative pathway. Binds two calcium ions per subunit. Binds one copper ion. Binding of one copper ion does not interfere with calcium binding. Required for the copper-dependent stress-induced export of IL1A and FGF1. The calcium-free protein binds to lipid vesicles containing phosphatidylserine, but not to vesicles containing phosphatidylcholine (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2617R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2617R-A350
Lokale Artikelnummer::
BOSSBS-2617R-A350
Beschreibung:
Plays a role in the export of proteins that lack a signal peptide and are secreted by an alternative pathway. Binds two calcium ions per subunit. Binds one copper ion. Binding of one copper ion does not interfere with calcium binding. Required for the copper-dependent stress-induced export of IL1A and FGF1. The calcium-free protein binds to lipid vesicles containing phosphatidylserine, but not to vesicles containing phosphatidylcholine (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15458R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15458R-A647
Lokale Artikelnummer::
BOSSBS-15458R-A647
Beschreibung:
Hephaestin is a single-pass type I membrane protein that belongs to the multicopper oxidase family of proteins. Hephaestin, a copper-dependant ferroxidase protein, is crucial for iron exiting intestinal enterocytes into the circulation. It mediates the movement of iron across the basolateral membrane in conjunction with ferroportin 1. This is an important link between iron and copper metabolism in mammalian systems, as copper deficiency leads to reduced hephaestin and reduced iron absorption resulting in anemia. Hephaestin can bind six copper ions per monomer and is regulated by the homeobox transcription factor CDX2. Increased levels of iron leads to an increase in CDX2 expression and thus Hephaestin. Hephaestin is primarily detected in the intestine, but is also expressed in colon, breast, bone trabecural cells and fibroblasts.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15458R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15458R-A680
Lokale Artikelnummer::
BOSSBS-15458R-A680
Beschreibung:
Hephaestin is a single-pass type I membrane protein that belongs to the multicopper oxidase family of proteins. Hephaestin, a copper-dependant ferroxidase protein, is crucial for iron exiting intestinal enterocytes into the circulation. It mediates the movement of iron across the basolateral membrane in conjunction with ferroportin 1. This is an important link between iron and copper metabolism in mammalian systems, as copper deficiency leads to reduced hephaestin and reduced iron absorption resulting in anemia. Hephaestin can bind six copper ions per monomer and is regulated by the homeobox transcription factor CDX2. Increased levels of iron leads to an increase in CDX2 expression and thus Hephaestin. Hephaestin is primarily detected in the intestine, but is also expressed in colon, breast, bone trabecural cells and fibroblasts.
VE:
1 * 100 µl
Artikel-Nr:
(A10954.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
A10954.06
Lokale Artikelnummer::
ALFAA10954.06
Beschreibung:
Stabilized with copper
VE:
1 * 5 g
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