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You Searched For: Potassium+(4-ethoxyphenyl)trifluoroborate


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Image Unavailable-BOSSBS-11048R-CY5

Anti-CUTC Rabbit Polyclonal Antibody (Cy5®)

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.
Catalog Number: BOSSBS-11048R-CY5
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-11048R-A647

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

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

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

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

Anti-CUTC Rabbit Polyclonal Antibody

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.
Catalog Number: BOSSBS-11048R
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-2617R-A750

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

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

Anti-S100 A13 Rabbit Polyclonal Antibody (Cy3®)

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).
Catalog Number: BOSSBS-2617R-CY3
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-A15334.18

Bromotrimethylsilane ≥97% stabilised

Description: Stabilized with copper powder or silver wire
Catalog Number: A15334.18
UOM: 1 * 50 g
Supplier: Thermo Fisher Scientific

MSDS Certificates


Image Unavailable-L17581.03

3-Iodothiophene 96% stabilised

Description: Stabilized with copper
Catalog Number: L17581.03
UOM: 1 * 1 g
Supplier: Thermo Fisher Scientific

MSDS Certificates


Image Unavailable-L05194.18

1-Iodo-3-methylbutane ≥97% stabilised

Description: Stabilized with copper
Catalog Number: L05194.18
UOM: 1 * 50 g
Supplier: Thermo Fisher Scientific

MSDS Certificates


Image Unavailable-BOSSBS-15458R-CY5

Anti-Hephaestin Rabbit Polyclonal Antibody (Cy5)

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.
Catalog Number: BOSSBS-15458R-CY5
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-15458R-A488

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

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.
Catalog Number: BOSSBS-15458R-A488
UOM: 1 * 100 µl
Supplier: Bioss
Product Image-ENZOBMLSE5350100

Human recombinant tyrosinase (from E. coli)

Description: Produced in <i>E. coli</i>. Tyrosinase is a copper-containing enzyme that catalyzes four steps in the melanin and catecholamine synthesis pathways.
Catalog Number: ENZOBMLSE5350100
UOM: 1 * 100 µG
Supplier: ENZO LIFE SCIENCES
Image Unavailable-A15883.22

1-Iodo-2-methylpropane ≥97% stabilised

Description: Stabilized with copper
Catalog Number: A15883.22
UOM: 1 * 100 g
Supplier: Thermo Fisher Scientific

MSDS Certificates


Image Unavailable-B23532.14

2-Ethylhexyl bromide 96% stabilised

Description: Stabilized with copper
Catalog Number: B23532.14
UOM: 1 * 25 g
Supplier: Thermo Fisher Scientific

MSDS Certificates


Image Unavailable-BOSSBS-8034R-CY5.5

Anti-COMMD1 Rabbit Polyclonal Antibody (Cy5.5®)

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.
Catalog Number: BOSSBS-8034R-CY5.5
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-11048R-A350

Anti-CUTC Rabbit Polyclonal Antibody (Alexa Fluor® 350)

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.
Catalog Number: BOSSBS-11048R-A350
UOM: 1 * 100 µl
Supplier: Bioss
497 - 512 of 25 890