Anti-NDUFB10 antibody [EPR16230-47] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal NDUFB10 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra), IHC-P and reacts with Human samples.
View Alternative Names
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10, Complex I-PDSW, NADH-ubiquinone oxidoreductase PDSW subunit, CI-PDSW, NDUFB10
- WB
Supplier Data
Western blot - Anti-NDUFB10 antibody [EPR16230-47] - BSA and Azide free (AB251216)
This data was developed using ab196019, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-NDUFB10 antibody [EPR16230-47] (<a href='/en-us/products/primary-antibodies/ndufb10-antibody-epr16230-47-ab196019'>ab196019</a>) at 1/10000 dilution
Lane 1:
HeLa (Human epithelial cells from cervix adenocarcinoma) cell lysate at 20 µg
Lane 2:
HepG2 (Human liver hepatocellular carcinoma) cell lysate at 20 µg
Lane 3:
Jurkat (Human T cell leukemia cells from peripheral blood) cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 21 kDa
Observed band size: 21 kDa
false
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-NDUFB10 antibody [EPR16230-47] - BSA and Azide free (AB251216)
This data was developed using ab196019, the same antibody clone in a different buffer formulation.
Intracellular Flow Cytometry analysis of HeLa (human cervix adenocarcinoma) cells labelling NDUFB10 (red) with purified ab196019 at a dilution of 1/800. The secondary antibody used was Alexa Fluor® 488 goat-anti-rabbit IgG (1/2000). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Isotype control antibody was rabbit monoclonal IgG (black). The blue line shows cells without incubation with primary and secondary antibody.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-NDUFB10 antibody [EPR16230-47] - BSA and Azide free (AB251216)
This data was developed using ab196019, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (Human epithelial cells from cervix adenocarcinoma) cells labeling NDUFB10 with ab196019 at 1/350 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Cytoplasm staining on HeLa cell line is observed. The nuclear counter stain is DAPI (blue).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NDUFB10 antibody [EPR16230-47] - BSA and Azide free (AB251216)
This data was developed using ab196019, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human transitional cell carcinoma of bladder tissue labeling NDUFB10 with ab196019 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasm staining on Human transitional cell carcinoma of bladder tissue is observed. Counter stained with Hematoxylin.
Secondary control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IP
Supplier Data
Immunoprecipitation - Anti-NDUFB10 antibody [EPR16230-47] - BSA and Azide free (AB251216)
This data was developed using ab196019, the same antibody clone in a different buffer formulation.
NDUFB10 was immunoprecipitated from HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell extract with ab196019 at 1/50 dilution. Western blot was performed from the immunoprecipitate using ab196019 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution.
Lane 1 : HeLa whole cell extract 10 μg (Input). Lane 2 : ab196019 IP in HeLa whole cell extract. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab196019 in HeLa whole cell extract.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-NDUFB10 antibody [EPR16230-47] (<a href='/en-us/products/primary-antibodies/ndufb10-antibody-epr16230-47-ab196019'>ab196019</a>)
Predicted band size: 21 kDa
false
Related conjugates and formulations (1)
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Anti-NDUFB10 antibody [EPR16230-47]
Reactivity data
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Properties and storage information
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Shipped at conditions
Appropriate short-term storage conditions
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Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
NDUFB10 plays a significant role in cellular energy production by being a subunit of complex I in the mitochondrial electron transport chain. As part of this large enzyme complex NDUFB10 contributes to the overall stability and function of complex I facilitating ATP production by driving the conversion of energy derived from nutrients into a usable form. Its presence in the mitochondrial inner membrane highlights its essential role in maintaining efficient energy metabolism and cellular respiration.
Pathways
The electron transport chain pathway incorporates NDUFB10 as a vital component. This pathway plays a major role in oxidative phosphorylation where NDUFB10 interacts closely with other mitochondrial proteins like NDUFS1 and NDUFA1 within complex I. Besides serving in ATP synthesis these interactions help in maintaining overall cellular bioenergetics and proper mitochondrial function demonstrating the integrated role NDUFB10 plays alongside other proteins in energy metabolism.
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