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Products:Tags & Cell Markers >> Subcellular Markers >> Organelles >> Mitochondria
MSCatalog No. MSP04
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Read our guarantee »Anti-Pyruvate Dehydrogenase E1 beta subunit antibody [17A5E2H8 ]
See all Pyruvate Dehydrogenase E1 beta subunit products (4) ...
Mouse monoclonal [17A5E2H8 ] to Pyruvate Dehydrogenase E1 beta subunit
Reacts with
Mouse, Rat, Cow, Human
Porcine Pyruvate Dehydrogenase E1 beta subunit protein.
Isolated mitochondria from Human, Bovine, Rat and Mouse hearts; HepG2 cell lysate.
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.02% Sodium azide
Constituent: HBS
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IgG fraction
ab110331 was produced in vitro using hybridomas grown in serum-free medium, and then purified by biochemical fractionation.
Monoclonal
17A5E2H8
IgG1
kappa
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Energy transfer pathways >> Energy Metabolism
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Carbohydrate metabolism
Metabolism >> Pathways and Processes >> Mitochondrial Metabolism >> Mitochondrial markers
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of carbohydrates
Signal Transduction >> Metabolism >> Mitochondrial
Signal Transduction >> Metabolism >> Energy Metabolism
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Mitochondria
Western blot - Pyruvate Dehydrogenase E1 beta subunit antibody [17A5E2H8 ] (ab110331)
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Our Abpromise guarantee covers the use of ab110331 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use a concentration of 1 µg/ml. Predicted molecular weight: 39 kDa.
The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). It contains multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3).
Defects in PDHB are a cause of pyruvate dehydrogenase E1 component deficiency (PDHE1 deficiency) [MIM:312170]. PDHE1 deficiency is the most common enzyme defect in patients with primary lactic acidosis. It is associated with variable clinical phenotypes ranging from neonatal death to prolonged survival complicated by developmental delay, seizures, ataxia, apnea, and in some cases to an X-linked form of Leigh syndrome (LS) (Leigh encephalomyelopathy).
Mitochondrion matrix.
Target information above from: UniProt accessionP11177
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Pyruvate Dehydrogenase E1 beta subunit antibody [17A5E2H8 ] (ab110331)
![Western blot - Pyruvate Dehydrogenase E1 beta subunit antibody [17A5E2H8 ] (ab110331)](/ps/datasheet/images/110/ab110331/Pyruvate-Dehydrogenase-E1-beta-subunit-Primary-antibodies-ab110331-1.jpg)
All lanes : Anti-Pyruvate Dehydrogenase E1 beta subunit antibody [17A5E2H8 ] (ab110331) at 1 µg/ml
Lane 1 : Isolated mitochondria from Human heart at 10 µg/ml
Lane 2 : Isolated mitochondria from Bovine heart at 4 µg/ml
Lane 3 : Isolated mitochondria from Rat heart at 10 µg/ml
Lane 4 : Isolated mitochondria from Mouse heart at 10 µg/ml
Lane 5 : HepG2 cell lysate at 20 µg/ml
Predicted band size : 39 kDa
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