Rabbit Recombinant Monoclonal NDUFS3 antibody. Carrier free. Suitable for IHC-P, IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
IHC-P | IP | WB | ICC/IF | Flow Cyt (Intra) | |
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Human | Tested | Tested | Tested | Tested | Tested |
Mouse | Predicted | Predicted | Predicted | Predicted | Predicted |
Rat | Predicted | Predicted | Predicted | Predicted | Predicted |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
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Species Mouse, Rat | Dilution info - | Notes - |
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Species Human | Dilution info - | Notes - |
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Species Mouse, Rat | Dilution info - | Notes - |
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Species Human | Dilution info - | Notes - |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
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Species Mouse, Rat | Dilution info - | Notes - |
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Species Human | Dilution info - | Notes - |
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Species Mouse, Rat | Dilution info - | Notes - |
Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which catalyzes electron transfer from NADH through the respiratory chain, using ubiquinone as an electron acceptor (PubMed:14729820, PubMed:30140060). Essential for the catalytic activity and assembly of complex I (PubMed:14729820, PubMed:24028823, PubMed:30140060).
Complex I-30kD, NADH-ubiquinone oxidoreductase 30 kDa subunit, CI-30kD, NDUFS3
Rabbit Recombinant Monoclonal NDUFS3 antibody. Carrier free. Suitable for IHC-P, IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ab249976 is the carrier-free version of Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471.
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.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
NADH:ubiquinone oxidoreductase core subunit S3 (NDUFS3) is an important component of the mitochondrial respiratory chain complex I also known as NADH:ubiquinone oxidoreductase. With an approximate mass of 25 kDa NDUFS3 plays an integral role in the assembly and function of complex I. This protein is mostly expressed in the mitochondria across various tissues. It is better known as a core subunit important for the catalytic activity of complex I.
NDUFS3 participates in cellular respiration by facilitating the electron transfer from NADH to ubiquinone. It is part of the complex I assembly that comprises 45 different subunits. This large assembly is the first enzyme of the mitochondrial electron transport chain and it ensures efficient energy production in the form of ATP. In its role NDUFS3 collaborates closely with other core subunits like NDUFS1 and NDUFS2 to maintain the proper function of cellular metabolism.
NDUFS3 is essential in the oxidative phosphorylation pathway which plays an important part in ATP generation. By interacting with other complex I subunits NDUFS3 enables electron flow that drives ATP synthase activity. Additionally it is connected to the apoptosis pathway. Its dysfunction may result in disrupted energy metabolism which can trigger cell death. NDUFS3 also interacts with proteins like NDUFV1 and NDUFV2 highlighting its centrality in energy and signal transduction processes.
NDUFS3 links to mitochondrial disorders and neurodegenerative diseases such as Leigh syndrome. Mutations in NDUFS3 can impair mitochondrial function leading to reduced ATP production and accumulation of defective mitochondria. These alterations contribute to the progressive deterioration seen in these disorders. In the context of neurodegenerative diseases NDUFS3 dysfunction may associate with proteins like cytochrome c emphasizing its role in mitochondria-dependent apoptotic pathways and neuronal health.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
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.
We do not recommend this combination. It is not covered by our product promise.
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This data was developed using the same antibody clone in a different buffer formulation (Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471).
Lanes 1 - 2: Merged signal (red and green). Green - Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 observed at 27 kDa. Red - loading control Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55kDa.
Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 was shown to react with NDUFS3 in HEK-293T wild-type cells in western blot with loss of signal observed in NDUFS3 knockout cell line Human NDUFS3 knockout HEK-293T cell line ab266419 (NDUFS3 knockout cell lysate Human NDUFS3 knockout HEK-293T cell lysate ab257556). Wild-type and NDUFS3 knockout HEK-293T cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1% Tween®) before incubation with Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 and Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4°C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-NDUFS3 antibody [EPR12782] - C-terminal (Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471) at 1/1000 dilution
Lane 1: Wild-type HEK-293T cell lysate at 20 µg
Lane 2: NDUFS3 knockout HEK-293T cell lysate at 20 µg
Lane 2: Western blot - Human NDUFS3 knockout HEK-293T cell line (Human NDUFS3 knockout HEK-293T cell line ab266419)
Performed under reducing conditions.
Predicted band size: 30 kDa
Observed band size: 27 kDa
This data was developed using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471, the same antibody clone in a different buffer formulation.Immunofluorescence analysis of 293 cells labeling NDUFS3 with Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 at 1/50 dilution (green). DAPI nuclear staining (blue).
This data was developed using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471, the same antibody clone in a different buffer formulation.
Intracellular Flow Cytometry analysis of HEK293 (Human embryonic kidney epithelial cell) cells labeling NDUFS3 (red) with purified Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 at a 1/200 dilution (10ug/mL). Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. A goat anti rabbit IgG (Alexa Fluor®488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody at a 1/2000 dilution. Black - Rabbit monoclonal IgG (Black) (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730). Blue (unlabeled control) - Cell without incubation with primary antibody and secondary antibody (Blue).
This data was developed using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471&
44; the same antibody clone in a different buffer formulation.
Western blot analysis on immunoprecipitation pellet from (1) human fetal heart lysate or (2) 1XPBS (negative control) using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 at 1/10 dilution, and HRP-conjugated anti-rabbit IgG preferentially detecting the non-reduced form of rabbit IgG.
All lanes: Immunoprecipitation - Anti-NDUFS3 antibody [EPR12782] - C-terminal (Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471)
Developed using the ECL technique.
Predicted band size: 30 kDa
This data was developed using the same antibody clone in a different buffer formulation (Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471).
Lanes 1- 4: Merged signal (red and green). Green - Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 observed at 30 kDa. Red - Anti-alpha Tubulin antibody [DM1A] - Loading Control (Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291) observed at 50 kDa.
Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 was shown to react with NDUFS3 in wild-type HEK-293T cells in western blot. Loss of signal was observed when knockout cell line Human NDUFS3 knockout HEK-293T cell line ab266419 (knockout cell lysate Human NDUFS3 knockout HEK-293T cell lysate ab257556) was used. Wild-type HEK-293T and NDUFS3 knockout HEK-293T cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 and Anti-alpha Tubulin antibody [DM1A] - Loading Control (Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291) overnight at 4°C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-NDUFS3 antibody [EPR12782] - C-terminal (Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471) at 1/1000 dilution
Lane 1: Wild-type HEK-293T cell lysate at 20 µg
Lane 2: NDUFS3 knockout HEK-293T cell lysate at 20 µg
Lane 2: Western blot - Human NDUFS3 knockout HEK-293T cell line (Human NDUFS3 knockout HEK-293T cell line ab266419)
Lane 3: HepG2 cell lysate at 20 µg
Lane 4: HL60 cell lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 30 kDa
Observed band size: 30 kDa
This data was developed using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471, the same antibody clone in a different buffer formulation.Immunohistochemcal analysis of paraffin-embedded Human heart tissue labeling NDUFS3 with Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 at 1/50 dilution. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
This data was developed using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471, the same antibody clone in a different buffer formulation.Immunohistochemcal analysis of paraffin-embedded Human kidney tissue labeling NDUFS3 with Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471 at 1/50 dilution. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
This data was developed using Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-NDUFS3 antibody [EPR12782] - C-terminal (Anti-NDUFS3 antibody [EPR12782] - C-terminal ab177471) at 1/1000 dilution
Lane 1: HepG2 lysate at 10 µg
Lane 2: 293T lysate at 10 µg
Lane 3: HL60 lysate at 10 µg
Lane 4: Fetal heart lysate at 10 µg
All lanes: Goat-anti-rabbit HRP at 1/2000 dilution
Developed using the ECL technique.
Predicted band size: 30 kDa
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