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You Searched For: Copper+(I)+telluride


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Devarda's alloy, Supelco®

Supplier: Merck
Description: Devarda's alloy, Supelco®

SDS

Image Unavailable-BOSSBS-2617R-CY5.5

Anti-S100 A13 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-2617R-CY5.5)
Supplier: Bioss
Description: 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).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-2617R-HRP

Anti-S100 A13 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-2617R-HRP)
Supplier: Bioss
Description: 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).
UOM: 1 * 100 µl
Image Unavailable-USBI167581

Anti-Copper Transporting ATPase1 Mouse Monoclonal Antibody [clone: S60-4]

Catalog Number: (USBI167581)
Supplier: US Biological
Description: Anti-Copper Transporting ATPase1 Mouse Monoclonal Antibody [clone: S60-4]
UOM: 1 * 100 µG
Image Unavailable-B23811.03

1-Iodo-4,4,4-trifluorobutane ≥98% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS

Image Unavailable-BOSSBS-1572R-CY7

Anti-ATP7A Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-1572R-CY7)
Supplier: Bioss
Description: May supply copper to copper-requiring proteins within the secretory pathway, when localised in the trans-Golgi network. Under conditions of elevated extracellular copper, it relocalised to the plasma membrane where it functions in the efflux of copper from cells.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-1572R-A647

Anti-ATP7A Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-1572R-A647)
Supplier: Bioss
Description: May supply copper to copper-requiring proteins within the secretory pathway, when localised in the trans-Golgi network. Under conditions of elevated extracellular copper, it relocalised to the plasma membrane where it functions in the efflux of copper from cells.
UOM: 1 * 100 µl
Image Unavailable-12844.22

Pentacopper silicide ≥99.5% (metals basis)

Supplier: Thermo Fisher Scientific
Description: Pentacopper silicide ≥99.5% (metals basis)

SDS Certificates

Image Unavailable-USBI167582

Anti-Copper Transporting ATPase2 Mouse Monoclonal Antibody [clone: S62-29]

Catalog Number: (USBI167582)
Supplier: US Biological
Description: Anti-Copper Transporting ATPase2 Mouse Monoclonal Antibody [clone: S62-29]
UOM: 1 * 100 µG
Image Unavailable-BOSSBS-11048R-CY5

Anti-CUTC Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-11048R-CY5)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11048R

Anti-CUTC Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-11048R)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8034R-A647

Anti-COMMD1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-8034R-A647)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-1572R

Anti-ATP7A Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-1572R)
Supplier: Bioss
Description: Copper-transporting ATPase 1 is an integral membrane protein cycling constitutively between the trans-golgi network and the plasma membrane. It may supply copper to copper-requiring proteins within the secretory pathway, when localized in the trans-golgi network. Under conditions of elevated extracellular copper, it relocalized to the plasma membrane where it functions in the efflux of copper from cells. Defects in ATP7A are the cause of Menkes syndrome; also known as kinky hair disease, an X-linked recessive disorder.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-1572R-CY5

Anti-ATP7A Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-1572R-CY5)
Supplier: Bioss
Description: May supply copper to copper-requiring proteins within the secretory pathway, when localised in the trans-Golgi network. Under conditions of elevated extracellular copper, it relocalised to the plasma membrane where it functions in the efflux of copper from cells.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11048R-A555

Anti-CUTC Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-11048R-A555)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11048R-A647

Anti-CUTC Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-11048R-A647)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on 0800 22 33 44
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Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
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The original product is no longer available. The replacement shown is available.
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