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Rabbit Anti-BAAT Antibody (CSB-PA613484ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Bile acid-CoA:amino acid N-acyltransferase1 Publication Antibody,Glycine N-choloyltransferase Antibody,Long-chain fatty-acyl-CoA hydrolase Antibody,BAAT AntibodyMore alternative names for the antibody
FLJ20300 antibody|BAAT antibody|BAAT_HUMAN antibody|BACAT antibody|BAT antibody|Bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase) antibody|Bile acid CoA:amino acid N acyltransferase antibody|Bile acid Coenzyme A amino acid N acyltransferase glycine N choloyltransferase antibody|Bile acid Coenzyme A: amino acid N acyltransferase antibody|Bile acid-CoA:amino acid N-acyltransferase antibody|Glycine N choloyltransferase antibody|Glycine N-choloyltransferase antibody|Long chain fatty acyl CoA hydrolase antibody|Long-chain fatty-acyl-CoA hydrolase antibody|MGC104432 antibody
Anti-BAAT antibody (ab83882)
Anti-BAAT antibody (ab83882)
Recommended applications: ELISA, WB, IHC
Recommended dilution: User optimized
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Bile acid-CoA:amino acid N-acyltransferase protein (309-418AA)
ELISA, WB, IHC
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:570( Human), Entrez Gene:12012( Mouse), Entrez Gene:29725( Rat), Omim:602938( Human), SwissProt:Q14032( Human), SwissProt:Q91X34( Mouse), SwissProt:Q63276( Rat), Unigene:284712( Human), Unigene:2859( Mouse), Unigene:11129( Rat)
|Protein function|| |
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. .
|Protein tissue specificity|| |
Expressed in liver, gallbladder mucosa and pancreas. .
|Involvement in disease|| |
Familial hypercholanemia (FHCA) [MIM:607748]: A disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption. . Note=The disease may be caused by mutations affecting distinct genetic loci, including the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the C/M/P thioester hydrolase family.
|Protein cellular localization|| |
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