Benzoic+acid-acyl-\\\\u03B2-D-glucuronide
Artikel-Nr:
(BOSSBS-5031R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5031R-FITC
Lokale Artikelnummer::
BOSSBS-5031R-FITC
Beschreibung:
Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. Acyl-coenzyme A Thioesterase 8, also known as ACOT8 may mediate Nef-induced down-regulation of CD4. It is a major thioesterase in peroxisomes and competes with BAAT (Bile acid CoA: amino acid N-acyltransferase) for bile acid-CoA substrate (such as chenodeoxycholoyl-CoA). It shows a preference for medium-length fatty acyl-CoAs and may be involved in the metabolic regulation of peroxisome proliferation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5031R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5031R-A555
Lokale Artikelnummer::
BOSSBS-5031R-A555
Beschreibung:
Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. Acyl-coenzyme A Thioesterase 8, also known as ACOT8 may mediate Nef-induced down-regulation of CD4. It is a major thioesterase in peroxisomes and competes with BAAT (Bile acid CoA: amino acid N-acyltransferase) for bile acid-CoA substrate (such as chenodeoxycholoyl-CoA). It shows a preference for medium-length fatty acyl-CoAs and may be involved in the metabolic regulation of peroxisome proliferation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7053R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7053R-HRP
Lokale Artikelnummer::
BOSSBS-7053R-HRP
Beschreibung:
Condensing enzyme that catalyzes the synthesis of polyunsaturated very long chain fatty acid (C20- and C22-PUFA). Acts specifically toward polyunsaturated acyl-CoA with the higher activity toward C20:4(n-6) acyl-CoA.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6019R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6019R
Lokale Artikelnummer::
BOSSBS-6019R
Beschreibung:
Aminoacylase 1 is a cytosolic, homodimeric, zinc binding enzyme that catalyzes the hydrolysis of acylated L amino acids to L amino acids and acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. ACY1 has been assigned to chromosome 3p21.1, a region reduced to homozygosity in small cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase 1 is highly homologous to the porcine counterpart, and ACY1 is the first member of a new family of zinc binding enzymes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-CY3
Lokale Artikelnummer::
BOSSBS-10150R-CY3
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5015R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-CY7
Lokale Artikelnummer::
BOSSBS-5015R-CY7
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12951R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12951R-CY3
Lokale Artikelnummer::
BOSSBS-12951R-CY3
Beschreibung:
AASDH is an Acyl CoA synthetase. Acyl CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA .
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12951R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12951R-CY7
Lokale Artikelnummer::
BOSSBS-12951R-CY7
Beschreibung:
AASDH is an Acyl CoA synthetase. Acyl CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA .
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12951R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12951R-HRP
Lokale Artikelnummer::
BOSSBS-12951R-HRP
Beschreibung:
AASDH is an Acyl CoA synthetase. Acyl CoA synthases catalyze the initial reaction in fatty acid metabolism, by forming a thioester with CoA .
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7053R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7053R-A350
Lokale Artikelnummer::
BOSSBS-7053R-A350
Beschreibung:
Condensing enzyme that catalyzes the synthesis of polyunsaturated very long chain fatty acid (C20- and C22-PUFA). Acts specifically toward polyunsaturated acyl-CoA with the higher activity toward C20:4(n-6) acyl-CoA.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R
Lokale Artikelnummer::
BOSSBS-10150R
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5119R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5119R-A555
Lokale Artikelnummer::
BOSSBS-5119R-A555
Beschreibung:
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate.[provided by RefSeq, Sep 2009]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5119R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5119R-CY3
Lokale Artikelnummer::
BOSSBS-5119R-CY3
Beschreibung:
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate.[provided by RefSeq, Sep 2009]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5119R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5119R-HRP
Lokale Artikelnummer::
BOSSBS-5119R-HRP
Beschreibung:
This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate.[provided by RefSeq, Sep 2009]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5023R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5023R
Lokale Artikelnummer::
BOSSBS-5023R
Beschreibung:
AGPAT1 converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5040R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5040R-CY7
Lokale Artikelnummer::
BOSSBS-5040R-CY7
Beschreibung:
Involved in bile acid metabolism. In liver hepatocytes catalyzes the second step in the conjugation of C24 bile acids (choloneates) to glycine and taurine before excretion into bile canaliculi. The major components of bile are cholic acid and chenodeoxycholic acid. In a first step the bile acids are converted to an acyl-CoA thioester, either in peroxisomes (primary bile acids deriving from the cholesterol pathway), or cytoplasmic at the endoplasmic reticulum (secondary bile acids). May catalyze the conjugation of primary or secondary bile acids, or both. The conjugation increases the detergent properties of bile acids in the intestine, which facilitates lipid and fat-soluble vitamin absorption. In turn, bile acids are deconjugated by bacteria in the intestine and are recycled back to the liver for reconjugation (secondary bile acids). May also act as an acyl-CoA thioesterase that regulates intracellular levels of free fatty acids. In vitro, catalyzes the hydrolysis of long- and very long-chain saturated acyl-CoAs to the free fatty acid and coenzyme A (CoASH), and conjugates glycine to these acyl-CoAs.
VE:
1 * 100 µl
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