Recombinant Human BCAT1 Protein, CF Summary
Details of Functionality |
Measured by its ability to convert leucine and alpha-ketoglutarate to alpha-ketoisocaproate and glutamate. The specific activity is >9,000 pmol/min/μg, as measured under the described conditions. |
Source |
E. coli-derived human BCAT1 protein Lys2-Ser386 with an N-terminal Met and 6-His tag
|
Accession # |
|
N-terminal Sequence |
Met |
Protein/Peptide Type |
Recombinant Enzymes |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
44 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
40-45 kDa, reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 6 months from date of receipt, -20 to -70 °C as supplied.
- 3 months, -20 to -70 °C under sterile conditions after opening.
|
Buffer |
Supplied as a 0.2 μm filtered solution in Tris, NaCl, DTT and Glycerol. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Assay Procedure |
- Assay Buffer: 50 mM Tris, 0.05% Tween-20, pH 8.0
- Recombinant Human BCAT1 (rhBCAT1) (Catalog # 9536-BA)
-
Recombinant
Human NQO-1 (rhNQO-1) (Catalog # 7567-DH)
- Glutamate dehydrogenase (GIDH) (Sigma, Catalog # G7882), 200 U/mL sock in 50 mM Tris, 0.05% Tween-20, pH 8.0
- Nicotinamide adenine dinucleotide ( beta -NAD) (Sigma, Catalog # N6522), 100 mM stock in deionized water
- Resazurin
(Catalog #
AR002)
- alpha -Ketoglutaric Acid (Sigma, Catalog # K2010), 1 M stock in deionized water
- L-Leucine (EMD Biosciences, Inc., Catalog # 4330), 100 mM stock in deionized water
- F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
- Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
- Dilute rhBCAT1 to 0.04 µg/mL in Assay Buffer.
- Dilute alpha -Ketoglutaric Acid to 100 mM in Assay Buffer.
- Prepare Substrate Mixture containing 100 U/mL GIDH, 2 mM beta -NAD, 40 µM Resazurin, 1 mM alpha -Ketoglutaric Acid, 4 mM L-Leucine, and 4 µg/mL rhNQO-1 in Assay Buffer.
- Load 50 µL of 0.04 µg/mL rhBCAT-1 in a plate, and start the reaction by adding 50 µL of Substrate Mixture. Include a Substrate Blank containing 50 µL Assay Buffer and 50 µL of Substrate Mixture.
- Read at excitation and emission wavelengths of 540 nm and 585 nm (top read), respectively, in kinetic mode for 8 minutes with a 3 minute lag time in kinetic mode.
- Calculate specific activity:
Specific Activity (pmol/min/µg) = | Adjusted Vmax* (RFU/min) x Conversion Factor** (pmol/RFU) | amount of enzyme (µg) |
*Adjusted for Substrate Blank. **Derived using calibration standard Resorufin (Sigma, Catalog # R3257). Per Well: - rhBCAT1: 0.002 µg
- GIDH: 5 U
- beta -NAD: 1 mM
- rhNQO-1: 0.2 µg
- Resazurin: 0.02 mM
- alpha -Ketoglutaric Acid: 0.5 mM
- L-Leucine: 2 mM
|
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human BCAT1 Protein, CF
Background
Branched-chain-amino-acid
aminotransferases (BCATs) are enzymes that catalyze the first reaction in the
catabolism of the essential branched-chain amino acids leucine, isoleucine, and
valine to their respective keto-acids while concurrently producing glutamate. BCATs
belong to the class-IV pyridoxal-phosphate-dependent (PLP-dependent)
aminotransferase family of enzymes (1). There are two BCAT isozymes in humans
and mammals, a mitochondrial form known as BCATm or BCAT2 and a cytosolic form
known as BCATc or BCAT1 that share 55% sequence identity. In humans and
rodents, BCATm is found in most tissues whereas BCATc is almost exclusively
present in the nervous system (2,3) where it is thought to play a role in
glutamate neurotransmitter metabolism (1, 4). The 43 kDa human BCATc exists as
an active homodimer and has a unique CXXC active site near the dimerization
domain (4). BCATc can be regulated by redox and is implicated as a marker for
oxidative stress (5,6) and linked to Alzheimers Disease and Dementia (7).
BCATc has been shown to cause cell proliferation (8) and significant evidence
has been found implicating BCATc in several types of cancer (8-10). In many
reports, BCATc can be further used as a marker or for diagnostic purposes in
cancers (11‑13).
- Hutson, S. (2001) Prog. Nucleic. Acid Res. Mol. Biol. 70:175
- Suryawan, A. et al. (1998) Am. J. Clin. Nutr. 68:72.
- Hall, T.R. et al. (1993) J. Biol. Chem. 268:3092.
- Yennawar, N. H. (2006) J. Biol. Chem. 281:39660.
- Coles, S.J. et al. (2012) Acta.Biochim. Biophys. Sin. 44:172.
- El Hindy, M. et al. (2014) Antioxid. Redox Signal 20:2497.
- Ashby, E.L. et al. (2017) Neurochem. Res. 42:306.
- Zhang, L. and J. Han (2017) Biochem. Biophys. Res. Commun. 486:224.
- Zhu, W. et al. (2017) Mol. Carcinog. 56:1570.
- Zheng, Y.H. et al. (2016) Liver Int. 36:1836.
- Young, G.P. et al. (2016) Cancer Med. 5:2763.
- Pedersen, S.K. (2015) BMC Cancer. 15:654.
- Diaz-Lagares, A. et al. (2016) Clin. Cancer Res. 22:3361.
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