Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal ENO1 antibody. Carrier free. Suitable for ICC/IF, WB, Flow Cyt (Intra), IHC-P and reacts with Human, Mouse samples.
View Alternative Names
ENO1L1, MBPB1, MPB1, ENO1, Alpha-enolase, 2-phospho-D-glycerate hydro-lyase, C-myc promoter-binding protein, Enolase 1, MBP-1, MPB-1, Non-neural enolase, Phosphopyruvate hydratase, Plasminogen-binding protein, NNE
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol fixed HeLa (human cervix adenocarcinoma epithelial cell) cells labeling ENO1 + ENO2 + ENO3 with ab222514 at 1/500 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on HeLa cell line.
Counterstains : ab195889 Anti-alpha Tubulin antibody [DM1A] (red) - Microtubule Marker (Alexa Fluor® 594) (1/200). DAPI (blue).
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed HeLa (human cervix adenocarcinoma epithelial cell) cell line labeling ENO1 + ENO2 + ENO3 with ab222514 at 1/800 (red) compared with an isotype control Rabbit monoclonal IgG (ab172730) (black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (blue). Secondary antibody Goat anti rabbit IgG Alexa Fluor® 488 (ab150077), at 1/2000 dilution was used as the secondary antibody.
- WB
Supplier Data
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lanes 1, 2, and 4 : 1 seconds; Lane 3 : 3 seconds.
Lanes 1 - 3:
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] (<a href='/en-us/products/primary-antibodies/eno1-eno2-eno3-antibody-epr19680-ab222514'>ab222514</a>) at 1/2000 dilution
Lane 4:
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] (<a href='/en-us/products/primary-antibodies/eno1-eno2-eno3-antibody-epr19680-ab222514'>ab222514</a>) at 1/10000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 10 µg
Lane 2:
Jurkat (human T cell leukemia T lymphocyte), whole cell lysate at 10 µg
Lane 3:
Human skeletal muscle at 10 µg
Lane 4:
MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 47 kDa
false
- WB
Supplier Data
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lanes 1-3 : 3 seconds; Lane 4 : 1 seconds.
All lanes:
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] (<a href='/en-us/products/primary-antibodies/eno1-eno2-eno3-antibody-epr19680-ab222514'>ab222514</a>) at 1/2000 dilution
Lane 1:
Human fetal heart at 10 µg
Lane 2:
Human fetal kidney at 10 µg
Lane 3:
Human fetal spleen at 10 µg
Lane 4:
Human fetal brain at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 47 kDa
false
- WB
Supplier Data
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lanes 1-2 : 3 seconds; Lane 3 : 1 seconds.
All lanes:
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] (<a href='/en-us/products/primary-antibodies/eno1-eno2-eno3-antibody-epr19680-ab222514'>ab222514</a>) at 1/1000 dilution
Lane 1:
His-tagged human ENO1 (aa2-434) recombinant protein, 10 ng
Lane 2:
His-tagged human ENO2 (aa1-434) recombinant protein, 10 ng
Lane 3:
His-tagged human ENO3 (aa1-434) recombinant protein, 10 ng
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 47 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded human clear cell carcinoma tissue labeling ENO1 + ENO2 + ENO3 with ab222514 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) ready to use. Membranous and nuclear staining on human clear cell kidney carcinoma is observed. Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) ready to use.
Perform heat mediated antigen retrieval with EDTA buffer pH 9 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded mouse pancreas tissue labeling ENO1 + ENO2 + ENO3 with ab222514 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) ready to use. Cytoplasmic and nuclear staining on the medium-small ducts of normal mouse pancreas is observed. Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) ready to use.
Perform heat mediated antigen retrieval with EDTA buffer pH 9 before commencing with IHC staining protocol.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol fixed MCF7 (human breast adenocarcinoma epithelial cell) cells labeling ENO1 + ENO2 + ENO3 with ab222514 at 1/500 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on MCF7 cell line.
Counterstains : ab195889 Anti-alpha Tubulin antibody [DM1A] (red) - Microtubule Marker (Alexa Fluor® 594) (1/200). DAPI (blue).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded human pancreas tissue labeling ENO1 + ENO2 + ENO3 with ab222514 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) ready to use. Cytoplasmic and nuclear staining on medium-small ducts of human pancreas (PMID : 19425054). Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) ready to use.
Perform heat mediated antigen retrieval with EDTA buffer pH 9 before commencing with IHC staining protocol.
- WB
Supplier Data
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] - BSA and Azide free (AB251571)
This data was developed using ab222514, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lanes 1, 2, and 4 : 3 minutes; Lane 3 : 1 minute; Lane 5 : 3 seconds.
All lanes:
Western blot - Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680] (<a href='/en-us/products/primary-antibodies/eno1-eno2-eno3-antibody-epr19680-ab222514'>ab222514</a>) at 1/2000 dilution
Lane 1:
Mouse brain at 10 µg
Lane 2:
Mouse spleen at 10 µg
Lane 3:
Mouse kidney at 10 µg
Lane 4:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 10 µg
Lane 5:
RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 47 kDa
false
Related conjugates and formulations (1)
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Anti-ENO1 + ENO2 + ENO3 antibody [EPR19680]
Reactivity data
Product details
ab251571 is the carrier-free version of ab222514.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. 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.
Compatibility
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The enolase family of isoenzymes acts as multifunctional catalysts and has roles beyond glycolysis. ENO1 serves as a plasminogen receptor on cell surfaces assisting in tissue remodeling and immune response. ENO2 often referred to as neuron-specific enolase (NSE) functions importantly in neural development and tumor cell metabolism. ENO3 or muscle-specific enolase contributes to muscle metabolism and energy turnover. While these proteins individually carry out essential tasks they also form a complex that facilitates efficient energy production and cellular regulation.
Pathways
The enolase enzymes integrate in the glycolytic and gluconeogenesis pathways central to energy metabolism. Glycolysis involves other key proteins like hexokinase and phosphofructokinase cooperating for glucose breakdown and energy release. In gluconeogenesis the enolases help generate glucose from non-carbohydrate sources important during fasting or intense exercise. Their activity along with related proteins impacts the efficiency and regulation of energy metabolism pathways.
Product protocols
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Target data
Additional targets
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com