Rabbit Recombinant Monoclonal NDUFA5 antibody. Suitable for WB and reacts with Human samples. Cited in 1 publication.
pH: 7.2
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
WB | |
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Human | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/1000 - 1/10000 | Notes - |
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Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone.
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5, Complex I subunit B13, Complex I-13kD-B, NADH-ubiquinone oxidoreductase 13 kDa-B subunit, CI-13kD-B, NDUFA5
Rabbit Recombinant Monoclonal NDUFA5 antibody. Suitable for WB and reacts with Human samples. Cited in 1 publication.
pH: 7.2
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
NDUFA5 also known as NADH:Ubiquinone Oxidoreductase Subunit A5 is part of the mitochondrial respiratory chain complex I. This protein has an approximate molecular mass of 15 kDa. NDUFA5 is expressed in many tissues but shows higher levels in energy-demanding organs such as the heart brain and skeletal muscle. It contributes to cellular respiration by assisting in electron transfer from NADH to ubiquinone which is critical in energy production.
NDUFA5 is an essential component of Complex I in the mitochondrial inner membrane. Complex I the largest enzyme complex of the mitochondrial electron transport chain consists of 45 subunits. NDUFA5 functions by aiding electron transfer through this complex. Proper function of NDUFA5 is vital for ATP generation through oxidative phosphorylation an important process in bioenergetics.
The role of NDUFA5 in the electron transport chain places it central to the oxidative phosphorylation pathway. This pathway also includes other complexes such as Complex III and IV which continue electron transfer leading to ATP synthesis. NDUFA5 interacts closely with other subunits within Complex I like NDUFS2 and forms a luminal proton gradient necessary for ATP production.
NDUFA5 mutations have links to mitochondrial Complex I deficiency a condition causing disorders in energy metabolism. This deficiency can lead to a wide range of clinical manifestations including Leigh syndrome a severe neurological disorder. NDUFA5 dysfunction affects energy-intensive tissues and its abnormal activity could involve other proteins in Complex I such as NDUFS4 which together contribute to the pathology of these mitochondrial disorders.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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All lanes: Western blot - Anti-NDUFA5 antibody [EPR15330] (ab183706) at 1/5000 dilution
Lane 1: HepG2 cell lysate at 20 µg
Lane 2: 293 cell lysate at 20 µg
Lane 3: HT-1376 cell lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution
Predicted band size: 13 kDa
Observed band size: 13 kDa
All lanes: Western blot - Anti-NDUFA5 antibody [EPR15330] (ab183706) at 1/20000 dilution
All lanes: Human fetal heart lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution
Predicted band size: 13 kDa
Observed band size: 13 kDa
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