BCKDHB Monoclonal antibody, PBS Only (Detector)
BCKDHB Monoclonal Antibody for Cytometric bead array, Indirect ELISA
Host / Isotype
Mouse / IgG1
Reactivity
human, mouse, rat
Applications
Cytometric bead array, Indirect ELISA
Conjugate
Unconjugated
CloneNo.
1D12C7
Cat no : 68596-1-PBS
Synonyms
Validation Data Gallery
Product Information
68596-1-PBS targets BCKDHB as part of a matched antibody pair:
MP50570-1: 68596-2-PBS capture and 68596-1-PBS detection (validated in Cytometric bead array)
MP50570-3: 68596-4-PBS capture and 68596-1-PBS detection (validated in Cytometric bead array)
Unconjugated mouse monoclonal antibody pair in PBS only (BSA and azide free) storage buffer at a concentration of 1 mg/mL, ready for conjugation.
This conjugation ready format makes antibodies ideal for use in many applications including: ELISAs, multiplex assays requiring matched pairs, mass cytometry, and multiplex imaging applications.Antibody use should be optimized by the end user for each application and assay.
Tested Reactivity | human, mouse, rat |
Host / Isotype | Mouse / IgG1 |
Class | Monoclonal |
Type | Antibody |
Immunogen | BCKDHB fusion protein Ag33802 |
Full Name | branched chain keto acid dehydrogenase E1, beta polypeptide |
Calculated Molecular Weight | 392 aa, 43 kDa |
Observed Molecular Weight | 35-37 kDa |
GenBank Accession Number | BC040139 |
Gene Symbol | BCKDHB |
Gene ID (NCBI) | 594 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Protein G purification |
Storage Buffer | PBS Only |
Storage Conditions | Store at -80°C. |
Background Information
Branched-chain alpha-keto acid dehydrogenase E1 component beta chain (BCKDHB; BCKDE1B; BCKDH E1-beta) is a subunit of the BCKDH complex, which is a mitochondrial enzyme in the degradation pathway for branched-chain amino acids (BCAA). Together with BCKDHA, BCKDHB forms the E1 subunit of this complex, whereas DBT and DLD are the E2 and E3 subunits, respectively. A deficiency of the BCKDH complex in humans causes maple syrup urine disease (MSUD), a severe neurometabolic disorder diagnosed by the detection alloisoleucine in plasma (MIM 248600). (PMID: 30709776)