BCKDHB Polyclonal antibody
BCKDHB Polyclonal Antibody for WB, IHC, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse, rat and More (1)
Applications
WB, IHC, RIP, ELISA
Conjugate
Unconjugated
Cat no : 13685-1-AP
Synonyms
Validation Data Gallery
Tested Applications
Positive WB detected in | mouse liver tissue, Transfected HEK-293 cells, rat liver tissue |
Positive IHC detected in | human colon cancer tissue, human stomach tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Recommended dilution
Application | Dilution |
---|---|
Western Blot (WB) | WB : 1:500-1:2000 |
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
Published Applications
WB | See 6 publications below |
IHC | See 3 publications below |
RIP | See 1 publications below |
Product Information
13685-1-AP targets BCKDHB in WB, IHC, RIP, ELISA applications and shows reactivity with human, mouse, rat samples.
Tested Reactivity | human, mouse, rat |
Cited Reactivity | human, mouse, sheep |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | BCKDHB fusion protein Ag4552 相同性解析による交差性が予測される生物種 |
Full Name | branched chain keto acid dehydrogenase E1, beta polypeptide |
Calculated molecular weight | 392 aa, 43 kDa |
Observed molecular weight | 37 kDa |
GenBank accession number | BC040139 |
Gene symbol | BCKDHB |
Gene ID (NCBI) | 594 |
RRID | AB_2877972 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
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)
Protocols
Product Specific Protocols | |
---|---|
WB protocol for BCKDHB antibody 13685-1-AP | Download protocol |
IHC protocol for BCKDHB antibody 13685-1-AP | Download protocol |
Standard Protocols | |
---|---|
Click here to view our Standard Protocols |
Publications
Species | Application | Title |
---|---|---|
Anim Sci J MiR-330-5p negatively regulates ovine preadipocyte differentiation by targeting branched-chain aminotransferase 2. | ||
Cell Rep SIRT4 is an early regulator of branched-chain amino acid catabolism that promotes adipogenesis. | ||
Cell Rep Branched-chain amino acid catabolism breaks glutamine addiction to sustain hepatocellular carcinoma progression | ||
Nat Commun AMPK induces degradation of the transcriptional repressor PROX1 impairing branched amino acid metabolism and tumourigenesis | ||
J Thromb Haemost Branched-chain amino acids promote thrombocytopoiesis by activating mTOR signaling | ||
Nucleic Acids Res Mitolnc controls cardiac BCAA metabolism and heart hypertrophy by allosteric activation of BCKDH |