Print…

You Searched For: Copper


2,041  results were found

Refine Results Sort by
SearchResultCount:"2041"

Sort Results

List View Easy View

Rate These Search Results

Image Unavailable-BOSSBS-15458R-CY3

Anti-Hephaestin Rabbit Polyclonal Antibody (Cy3)

Catalog Number: (BOSSBS-15458R-CY3)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-2617R-A750

Anti-S100A13 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-2617R-A750)
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-1718R-HRP

Anti-ATP7B Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-1718R-HRP)
Supplier: Bioss
Description: Involved in the export of copper out of the cells, such as the efflux of hepatic copper into the bile.
UOM: 1 * 100 µl
Image Unavailable-A11032.09

Chloroiodomethane ≥98% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-BOSSBS-2617R-CY3

Anti-S100 A13 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-2617R-CY3)
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-A14658.22

2-Iodoethanol ≥99% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-BOSSBS-15458R-CY5

Anti-Hephaestin Rabbit Polyclonal Antibody (Cy5)

Catalog Number: (BOSSBS-15458R-CY5)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-A12977.22

1-Iodohexadecane ≥98% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-BOSSBS-10529R-CY7

Anti-AOC3 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-10529R-CY7)
Supplier: Bioss
Description: This gene encodes a member of the semicarbazide-sensitive amine oxidase family. Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of Copper and quinone cofactor. The encoded protein is localized to the cell surface, has adhesive properties as well as monoamine oxidase activity, and may be involved in leukocyte trafficking. Alterations in levels of the encoded protein may be associated with many diseases, including diabetes mellitus. A pseudogene of this gene has been described and is located approximately 9-kb downstream on the same chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]
UOM: 1 * 100 µl
Image Unavailable-B20619.18

2-Iodobutane ≥99% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-BOSSBS-15458R-A488

Anti-Hephaestin Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

Catalog Number: (BOSSBS-15458R-A488)
Supplier: Bioss
Description: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8034R-CY7

Anti-COMMD1 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-8034R-CY7)
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-B25391.14

(Iodomethyl)cyclopentane ≥98% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-L01522.14

Iodocyclopentane ≥97% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-A15066.22

2-Iodopropane ≥98% stabilised

Supplier: Thermo Fisher Scientific
Description: Stabilized with copper

SDS Certificates

Image Unavailable-BOSSBS-11048R-A680

Anti-CUTC Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-11048R-A680)
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 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.
UOM: 1 * 100 µl
Inquire for Price
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.
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
Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalogue Number listed above. If you need further assistance, please call VWR Customer Service on 0800 22 33 44.
417 - 432 of 2,041
no targeter for Bottom