7433 Results for: "2-Fluoro-6-(trifluoromethyl)benzyl+bromide&pageNo=27&view=easy"

Supplier: MACHEREY-NAGEL

Filter paper circles MN 612 27cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 617 27cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 640 w 27cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 918 27cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 960 27cm diameter, pack of 100. 1 * 100 items

Supplier: Bioss

Acyl-coenzyme A synthetases (ACSs) are a large family of related enzymes known to catalyze the fundamental initial reaction in fatty acid metabolism. The ACS family is roughly characterized based on fatty acid chain length preference amongst different members. The nomenclature in the ACS family reflects this relationship and includes short-chain ACS (ACSS), medium-chain ACS (ACSM), long-chain ACS (ACSL) and very long-chain ACS (ACSVL). ACSVL family members are capable of activating both long (LCFAs) and very long-chain fatty acids (VLCFAs). There are six members of the human ACSVL subfamily, which have been described as solute carrier family 27A (SLC27A) gene products. They represent a group of evolutionarily conserved fatty acid transport proteins (FATPs) recognized for their role in facilitating translocation of long-chain fatty acids across the plasma membrane. The family nomenclature has recently been unified with their respective acyl-CoA synthetase family designations: ACSVL1 (FATP2), ACSVL2 (FATP6), ACSVL3 (FATP3), ACSVL4 (FATP1), ACSVL5 (FATP4) and ACSVL6 (FATP5). ACSVLs have unique expression patterns and are found in major organs of fatty acid metabolism, such as adipose tissue, liver, heart and kidney. ACSVL2 is a 619 amino acid multi-pass membrane protein. Encoded by a gene that maps to human chromosome 5q23.3, ACSVL2 may function as the predominant fatty acid protein transporter in heart.

Supplier: Sartorius Balances

The Cubis® II laboratory balances are modular, therefore they allow to choose between applications and configurations which suit the best to the needs. These balances can be configured at the level of display, draftshields, software applications and hardware functions.

Supplier: Korff

ALU-SHEETS SOFT 0,020X500X700MM 1 * 100 items

Supplier: DELTALAB

RACK 200X70X60MM CAPACITY (6X2) 28MM 1 * 1 items

Supplier: DWK Life Sciences

Tube centrifuge, ar-glass, 100mm, round, bottom. 1 * 100 items

Supplier: Bioss

Acyl-coenzyme A synthetases (ACSs) are a large family of related enzymes known to catalyze the fundamental initial reaction in fatty acid metabolism. The ACS family is roughly characterized based on fatty acid chain length preference amongst different members. The nomenclature in the ACS family reflects this relationship and includes short-chain ACS (ACSS), medium-chain ACS (ACSM), long-chain ACS (ACSL) and very long-chain ACS (ACSVL). ACSVL family members are capable of activating both long (LCFAs) and very long-chain fatty acids (VLCFAs). There are six members of the human ACSVL subfamily, which have been described as solute carrier family 27A (SLC27A) gene products. They represent a group of evolutionarily conserved fatty acid transport proteins (FATPs) recognized for their role in facilitating translocation of long-chain fatty acids across the plasma membrane. The family nomenclature has recently been unified with their respective acyl-CoA synthetase family designations: ACSVL1 (FATP2), ACSVL2 (FATP6), ACSVL3 (FATP3), ACSVL4 (FATP1), ACSVL5 (FATP4) and ACSVL6 (FATP5). ACSVLs have unique expression patterns and are found in major organs of fatty acid metabolism, such as adipose tissue, liver, heart and kidney. ACSVL2 is a 619 amino acid multi-pass membrane protein. Encoded by a gene that maps to human chromosome 5q23.3, ACSVL2 may function as the predominant fatty acid protein transporter in heart.

Supplier: Sartorius Balances

The Cubis® II laboratory balances are modular, therefore they allow to choose between applications and configurations which suit the best to the needs. These balances can be configured at the level of display, draftshields, software applications and hardware functions.

Supplier: MACHEREY-NAGEL

Filter paper folded MN 616 WA 1/4 27cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper folded MN 619 eh 1/4 27cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper folded MN 619 de 1/4 27cm diameter, pack of 100. 1 * 100 items

Supplier: Bioss

Acyl-coenzyme A synthetases (ACSs) are a large family of related enzymes known to catalyze the fundamental initial reaction in fatty acid metabolism. The ACS family is roughly characterized based on fatty acid chain length preference amongst different members. The nomenclature in the ACS family reflects this relationship and includes short-chain ACS (ACSS), medium-chain ACS (ACSM), long-chain ACS (ACSL) and very long-chain ACS (ACSVL). ACSVL family members are capable of activating both long (LCFAs) and very long-chain fatty acids (VLCFAs). There are six members of the human ACSVL subfamily, which have been described as solute carrier family 27A (SLC27A) gene products. They represent a group of evolutionarily conserved fatty acid transport proteins (FATPs) recognized for their role in facilitating translocation of long-chain fatty acids across the plasma membrane. The family nomenclature has recently been unified with their respective acyl-CoA synthetase family designations: ACSVL1 (FATP2), ACSVL2 (FATP6), ACSVL3 (FATP3), ACSVL4 (FATP1), ACSVL5 (FATP4) and ACSVL6 (FATP5). ACSVLs have unique expression patterns and are found in major organs of fatty acid metabolism, such as adipose tissue, liver, heart and kidney. ACSVL2 is a 619 amino acid multi-pass membrane protein. Encoded by a gene that maps to human chromosome 5q23.3, ACSVL2 may function as the predominant fatty acid protein transporter in heart.

Supplier: Merck

Direct-Q® 3 systems have been developed for simple, immediate use. Ultrapure Type I water is suitable for preparing buffers for liquid chromatography and biochemical experiments, and for analytical procedures such as spectrophotometry and spectroscopy. For applications that require very low values of organic impurities, the Direct-Q® 3 UV system includes a UV lamp with two wavelengths in order to produce water with a TOC content <5 ppb, which is suitable for HPLC, GC, ILC and TOC analyses. With the BioPak™ cartridge as a final filter, Direct-Q® 3 systems produce pyrogen- and RNase-free water at a flow rate of 0,2 L/min. Direct-Q® 3 systems are ideal for laboratories which do not have easy access to pre-treated water and require between 5 and 10 litres of ultrapure water per day. For the production of Type I and Type III water.

Supplier: bimos

Apart from special hygiene features, a laboratory chair must always be ready for use at changing places of work. It should take up a minimum of space yet still offer maximum ergonomics and seating comfort so as to guarantee precise and concentrated work over longer periods of time. Labster is ideal for everyday use in the laboratory.

Supplier: ProSci Inc.

he activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. CRSP8 is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. CRSP8 is also a component of other multisubunit complexes e.g. thyroid hormone receptor- (TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors.The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor- (TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors.

Supplier: DELTALAB

RACK D=30MM 10X5 H=60 1 * 1 items

Supplier: MP Biomedicals

Storage: Store at Room Temperature (15-30 °C).
Ethylenediamine Tetraacetic Acid is a polyamino carboxylic acid hexadentate ligand and a chelating agent. This product is designated as Molecular Biology grade and is suitable for molecular biology applications.
Ethylenediamine Tetraacetic Acid is a chelator of divalent cations. It also inhibits enzymes, such as metalloproteases, that require divalent cations for activity.

Supplier: ProSci Inc.

CYP27A1 is a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Supplier: Thermo Fisher Scientific

O-RING INNER DIAMETER 0.799X0.103 EPR 60 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIG PP RED 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIG PP ORANGE 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIG PP BLUE 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIGPPNEONORANGE 1 * 1 items

Supplier: GERING

HYDROMETER F/OILS 0,995-1,015 W/+13+27C 1 * 1 items

Supplier: Amarell

Saccharimeter type Java, type I, 2-13,5:0,1Java, with therm. +20+40:0,5C with red or blue special liquid, ref. temp. 27,5C, 550mm long, temperature correction scale, special design 1 * 1 items

Supplier: MEMMERT

IQ/OQ/PQ CHECK LIST WORK TEST DATA F.IFBW 1 * 1 items