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

BCKDHB, E1B



Tested Applications

Positive WB detected inmouse liver tissue, Transfected HEK-293 cells, rat liver tissue
Positive IHC detected inhuman 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

ApplicationDilution
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.

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 Reactivityhuman, mouse, sheep
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen BCKDHB fusion protein Ag4552
Full Name branched chain keto acid dehydrogenase E1, beta polypeptide
Calculated Molecular Weight 392 aa, 43 kDa
Observed Molecular Weight37 kDa
GenBank Accession NumberBC040139
Gene Symbol BCKDHB
Gene ID (NCBI) 594
RRIDAB_2877972
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

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-APDownload protocol
IHC protocol for BCKDHB antibody 13685-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanIHC

Nat Cancer

Integrative proteogenomic profiling of high-risk prostate cancer samples from Chinese patients indicates metabolic vulnerabilities and diagnostic biomarkers

Authors - Baijun Dong
sheepWB

Anim Sci J

MiR-330-5p negatively regulates ovine preadipocyte differentiation by targeting branched-chain aminotransferase 2.

Authors - Tao Shi
mouseWB

Cell Rep

SIRT4 is an early regulator of branched-chain amino acid catabolism that promotes adipogenesis.

Authors - Elma Zaganjor
humanWB

Cell Rep

Branched-chain amino acid catabolism breaks glutamine addiction to sustain hepatocellular carcinoma progression

Authors - Dongdong Yang
humanIHC

Nat Commun

AMPK induces degradation of the transcriptional repressor PROX1 impairing branched amino acid metabolism and tumourigenesis

Authors - Yanan Wang
mouseWB

J Thromb Haemost

Branched-chain amino acids promote thrombocytopoiesis by activating mTOR signaling

Authors - Haojie Jiang