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Recombinant Human DBT/BCOADC-E2 Protein, N-His

CAT: 0013-GTR19072415-01Size: 20 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR19072415-01Size:20 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Recombinant Human DBT/BCOADC-E2 Protein, N-His, expressed in E.coli, with a molecular weight of 26.92 kDa, and a purity of >90% as determined by SDS-PAGE. It was purified by AC, and has a N-His tag.
Product Name Alternative
Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; mitochondrial; 2.3.1.168; 52 kDa mitochondrial autoantigen of primary biliary cirrhosis; Branched chain 2-oxo-acid dehydrogenase complex component E2; BCOADC-E2; Branched-chain alpha-keto acid dehydrogenase complex component E2; BCKAD-E2; BCKADE2; BCKDH-E2; Dihydrolipoamide acetyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; Dihydrolipoamide branched chain transacylase; Dihydrolipoyllysine-residue (2-methylpropanoyl) transferase; DBT; BCATE2; BCKDHE2
UniProt
P11182
Tag
N-His
Origin
Human
Purity
>90% as determined by SDS-PAGE.
Form
Lyophilized
Molecular Weight
26.92 kDa
Storage Conditions
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Notes
For research use only.
Preservative
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
AA Sequence
258-482/482

UniProtKB · P11182

Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial

ODB2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P11182
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
DBT
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.3.1.168
Processing
Precursor
Secondary accessions
B2R811, Q5VVL8
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Molecular function

AcyltransferaseTransferase

Disease

Disease variantMaple syrup urine disease

Domain

LipoylTransit peptide

Cellular component

Mitochondrion

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