Anti-ME2 antibody [EPR7218] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal ME2 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB, Flow Cyt (Intra) and reacts with Human samples.
View Alternative Names
NAD-ME, Malic enzyme 2, ME2
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human colon tissue sections labeling Me2 with Purified ab126616 at 1 : 1000 dilution (1.4 μg/ml). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). Tissue was counterstained with Hematoxylin. ImmunoHistoProbe one step HRP Polymer (ready to use) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
Unpurified ab126616, at 1/100 dilution, staining ME2 in HeLa cells by Immunofluorescence.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
Intracellular Flow Cytometry analysis of Jurkat (Human T cell leukemia T lymphocyte) cells labeling ME2 with purified ab126616 at 1/150 dilution (10 ug/ml) (red). Cells were fixed with 4% Paraformaldehyde and permeabilized with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488) secondary antibody was used at 1/2000 dilution. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- WB
Unknown
Western blot - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-ME2 antibody [EPR7218] (<a href='/en-us/products/primary-antibodies/me2-antibody-epr7218-ab126616'>ab126616</a>) at 1/1000 dilution
Lane 1:
293T (Human embryonic kidney epithelial cell) cell lysate at 10 µg
Lane 2:
Jurkat cell lysate at 10 µg
Lane 3:
HeLa cell lysate at 10 µg
Lane 4:
K562 cell lysate at 10 µg
Lane 5:
MOLT4 cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-rabbit HRP at 1/2000 dilution
Predicted band size: 65 kDa
false
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
Unpurified ab126616, at 1/50 dilution, staining ME2 in Formalin-fixed, Paraffin-embedded Human colon tissue by Immunohistochemistry.
Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
Immunocytochemistry/ Immunofluorescence analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling ME2 with purified ab126616 at 1 : 150 dilution (9.1μg/ml). Cells were fixed in 100% Methanol. ab150077 Goat anti rabbit IgG(Alexa Fluor® 488) was used as the secondary antibody at 1 : 1000 dilution. DAPI nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- WB
Lab
Western blot - Anti-ME2 antibody [EPR7218] - BSA and Azide free (AB248127)
This data was developed using ab126616, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ME2 antibody [EPR7218] (<a href='/en-us/products/primary-antibodies/me2-antibody-epr7218-ab126616'>ab126616</a>) at 1/5000 dilution
Lane 1:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 15 µg
Lane 2:
293T (Human embryonic kidney epithelial cell) whole cell lysates at 15 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 1/20000 dilution
Predicted band size: 65 kDa
false
Related conjugates and formulations (1)
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Anti-ME2 antibody [EPR7218]
Reactivity data
Product details
ab248127 is the carrier-free version of ab126616.
Species reactivity
Mouse: We have preliminary internal testing data to indicate this antibody may not react with this species.
Please contact us for more information.
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
ME2 is an important regulator of cellular metabolism and part of the mitochondrial malate-aspartate shuttle. The enzyme helps facilitate the transfer of reducing equivalents across the mitochondrial membrane. ME2 does not function alone and might interact with other metabolite transporters in mitochondrial membranes contributing to the balance of metabolic intermediates and maintenance of cellular energy homeostasis.
Pathways
Malate metabolism and energy production involve ME2's role in the tricarboxylic acid cycle and glycolysis. The tricarboxylic acid cycle requires ME2 for effective conversion of nutrients into usable energy. ME2 links with other metabolic enzymes including citrate synthase for efficient energy flow. Additionally the enzyme's activity affects the synthesis of biosynthetic intermediates integrating nutrient signals with bioenergetic demands.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
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