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Products:Tags & Cell Markers >> Subcellular Markers >> Organelles >> Mitochondria
MSCatalog No. MS783
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Read our guarantee »Anti-MDH2 antibody [2F5AF8]
See all MDH2 products (4) ...
Mouse monoclonal [2F5AF8] to MDH2
ICC/IF, In-Cell ELISA, IPmore details
Reacts with
Mouse, Rat, Human, Pig
Fibroblast cells Human heart homogenate Rat liver homogenate Mouse liver homogenate HepG2 whole cell lysate
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.02% Sodium azide
Concentration information loading...
>95% by SDS-PAGE
The antibody was produced in vitro using hybridomas grown in serum-free medium, and then purified by biochemical fractionation.
Monoclonal
2F5AF8
IgG1
kappa
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Energy transfer pathways >> Energy Metabolism
Metabolism >> Pathways and Processes >> Mitochondrial Metabolism >> Mitochondrial markers
Signal Transduction >> Metabolism >> Mitochondrial
Signal Transduction >> Metabolism >> Energy Metabolism
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Mitochondria
Our Abpromise guarantee covers the use of ab110317 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use a concentration of 1 - 4 µg/ml.
In-Cell ELISA: Use a concentration of 4 µg/ml.
IP: Use at an assay dependent dilution.
Belongs to the LDH/MDH superfamily. MDH type 1 family.
Acetylation is enhanced by up to 67% after treatment either with trichostin A (TSA) or with nicotinamide (NAM) with the appearance of tri-and tetraacetylations. Glucose also increases acetylation by about 60%.
Mitochondrion matrix.
Target information above from: UniProt accessionP40926
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - MDH2 antibody [2F5AF8] (ab110317)
![Immunocytochemistry/ Immunofluorescence - MDH2 antibody [2F5AF8] (ab110317)](/ps/datasheet/images/110/ab110317/MDH2-Primary-antibodies-ab110317-2.gif)
Immunocytochemistry image of stained fibroblast cells. The cells were paraformaldehyde fixed (4%, 20 minutes) and Triton X-100 permeabilized (0.1%, 15 min). The cells were incubated with the ab110317 (1 µg/mL) for 2 hours at room temperature or over night at 4°C. The secondary antibody was (red) Alexa Fluor® 594 goat anti-mouse IgG (H+L) at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. The target protein locates to the mitochondrial matrix
Immunoprecipitation - MDH2 antibody [2F5AF8] (ab110317)
![Immunoprecipitation - MDH2 antibody [2F5AF8] (ab110317)](/ps/datasheet/images/110/ab110317/MDH2-Primary-antibodies-ab110317-3.gif)
ab110317 pulls down the 33kDa MDH2 protein from Human heart homogenate (1), Rat liver homogenate (2), Mouse liver homogenate (3) and HepG2 whole cell lysate (4). The identity of this protein was confirmed by mass spectrometry. This gel was stained with coomassie.
ab110317 has not yet been referenced specifically in any publications.
Publishing research using ab110317? Please let us know so that we can cite the reference in this datasheet
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![Immunocytochemistry/ Immunofluorescence - MDH2 antibody [2F5AF8] (ab110317)](/ps/datasheet/images/110/ab110317/MDH2-Primary-antibodies-ab110317-2.gif)
Immunocytochemistry image of stained fibroblast cells. The cells were paraformaldehyde fixed (4%, 20 minutes) and Triton X-100 permeabilized (0.1%, 15 min). The cells were incubated with the ab110317 (1 µg/mL) for 2 hours at room temperature or over night at 4°C. The secondary antibody was (red) Alexa Fluor® 594 goat anti-mouse IgG (H+L) at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. The target protein locates to the mitochondrial matrix
![Immunoprecipitation - MDH2 antibody [2F5AF8] (ab110317)](/ps/datasheet/images/110/ab110317/MDH2-Primary-antibodies-ab110317-3.gif)
ab110317 pulls down the 33kDa MDH2 protein from Human heart homogenate (1), Rat liver homogenate (2), Mouse liver homogenate (3) and HepG2 whole cell lysate (4). The identity of this protein was confirmed by mass spectrometry. This gel was stained with coomassie.
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