BAAT Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
-
- Target See all BAAT Proteins
- BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 2
-
Origin
- Human
-
Source
- HEK-293 Cells
- Purification tag / Conjugate
- This BAAT protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
-
- Recombinant human BAAT (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product BAAT Protein
-
-
- Application Notes
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
-
The tag is located at the C-terminal.
- Restrictions
- For Research Use only
-
- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
-
- Target
- BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
- Alternative Name
- Baat (BAAT Products)
- Synonyms
- BACAT Protein, BAT Protein, AI118337 Protein, AI158864 Protein, kan-1 Protein, BAAT Protein, bile acid-CoA:amino acid N-acyltransferase Protein, Bile acid-CoA:amino acid N-acyltransferase Protein, bile acid-Coenzyme A: amino acid N-acyltransferase Protein, bile acid CoA:amino acid N-acyltransferase Protein, BAAT Protein, RPIC_RS10270 Protein, Bcav_2277 Protein, Rpic12D_1765 Protein, Baat Protein, LOC481635 Protein, LOC100054567 Protein, LOC786798 Protein
- Background
- The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene.
- Molecular Weight
- 46.1 kDa
- NCBI Accession
- NP_001121082
-