42973 Results for: "2-[Benzyl(2-hydroxyethyl)amino]-1-ethanol"

Supplier: Thermo Fisher Scientific

Mitomycin C, 5 mg/ml in DMSO, sterile-filtered 1 * 1 mL

Supplier: Merck

3-NITROPHENETHYL ALCOHOL, 98% 1 * 1 g

Supplier: Abcam

Human monoclonal [CR3022] to SARS-CoV-2 Spike Glycoprotein S1.

Supplier: Abcam

Product to be used as a negative control for ErbB 2 Affibody® Molecule Imaging Agent.

Supplier: Merck

(S)-(-)-ALPHA-METHYL-2-NAPHTHALENE-METHA NOL, 98% 1 * 1 g

Supplier: Merck

3-(TRIFLUOROMETHYL)PHENETHYL ALCOHOL, 99 % 1 * 1 g

Supplier: Merck

(+/-)-4-METHOXY-ALPHA-METHYLBENZYL ALCOH OL, 99% 1 * 25 mL

Supplier: Merck

2-NITROPHENETHYL ALCOHOL, 97% 1 * 10 g

Supplier: Merck

3,4-DIMETHOXYPHENETHYL ALCOHOL, 98% 1 * 50 g

Supplier: Merck

3,4-DIMETHOXYPHENETHYL ALCOHOL, 98% 1 * 10 g

Supplier: Honeywell Chemicals

ETHYL ALCOHOL 100% ALCOHOL HPLC GRADE 1 * 2 L

Supplier: Merck

ETHYL-13C2 ALCOHOL, 98 ATOM % 13C 1 * 1 g

Supplier: VARIAN

Bond Elut™ NH₂ is a weaker anion exchanger than sorbents such as SAX (a quaternary amine sorbent that is always charged) and is therefore a better choice for retention of very strong anions, such as sulfonic acids, which may retain irreversibly on a SAX sorbent. Similar to Diol and SI sorbents, Bond Elut™ NH₂ is excellent for the separation of structural isomers.

Supplier: Merck

ETHYL-2-13C ALCOHOL, 98 ATOM % 13C 1 * 1 g

Supplier: Merck

ETHYL-13C2 ALCOHOL, 98 ATOM % 13C 1 * 250 mg

Supplier: Merck

HOMOVANILLYL ALCOHOL, 99% 1 * 10 g

Supplier: Abcam

Mouse monoclonal [M8-P1-A3] to alpha 1 Sodium Potassium ATPase.

Supplier: Merck

HOMOVANILLYL ALCOHOL, 99% 1 * 2,5 g

Supplier: GASTEC

GASTUBE ETHYL ALCOHOL DOSI 100-25000PPM 1 * 10 items

Supplier: asecos

spray can stainless steel with support made of polypropylene, content 1 l 1 * 1 items

Supplier: Merck

(S)-4-BENZYLTHIAZOLIDINE-2-THIONE, >=97.0% 1 * 1 g

Supplier: Merck

(R)-4-BENZYLOXAZOLIDINE-2-THIONE, >=97.0% 1 * 1 g

Supplier: Merck

METHYL (S)-(-)-N-Z-AZIRIDINE-2-CARBOXYL& 1 * 5 g

Supplier: Merck

1-PIPERONYLPIPERAZINE, 97% 1 * 25 g

Supplier: Merck

N-METHYL-N-PROPARGYLBENZYLAMINE, 97% 1 * 5 g

Supplier: Merck

N-METHYL-N-PROPARGYLBENZYLAMINE, 97% 1 * 25 g

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.