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Products:Tags & Cell Markers >> Subcellular Markers >> Organelles >> Mitochondria
MSCatalog No. MS718
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Read our guarantee »Anti-ACAT1 antibody [9H10AB4]
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Mouse monoclonal [9H10AB4] to ACAT1
ICC, Flow Cyt, IP, IHC-P, In-Cell ELISAmore details
Reacts with
Human
Human liver mitochondria
ICC: Human HDFn cells IHC-P: Human cerebellum IP: HepG2 cells and Human liver mitochondria FC: HeLa cells
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.02% Sodium azide
Constituent: HBS
Concentration information loading...
Ammonium Sulphate Precipitation
Purity near homogeneity as judge by SDS-PAGE. The antibody was produced in-vitro using hybridomas grown in serum-free medium and then purified by biochemical fractionation.
Monoclonal
9H10AB4
IgG2a
kappa
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Amino acid metabolism
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Lipid and lipoprotein metabolism >> Lipid metabolism
Metabolism >> Pathways and Processes >> Mitochondrial Metabolism >> Mitochondrial markers
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of lipids and lipoproteins
Cardiovascular >> Lipids / Lipoproteins >> Fatty Acids >> Metabolism
Signal Transduction >> Metabolism >> Lipid metabolism
Signal Transduction >> Metabolism >> Mitochondrial
Signal Transduction >> Metabolism >> Amino Acids
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Peroxisome
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Mitochondria
Our Abpromise guarantee covers the use of ab110290 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC: Use a concentration of 5 µg/ml.
Flow Cyt: Use a concentration of 1 µg/ml.
IP: Use at an assay dependent dilution.
IHC-P: 1/100. Perform heat mediated antigen retrieval via the pressure cooker method (1 minute, with 1 mmol EDTA at pH8) before commencing with IHC staining protocol.
In-Cell ELISA: Use a concentration of 0.4 µg/ml. (0.4 µg/well)
Plays a major role in ketone body metabolism.
Defects in ACAT1 are a cause of 3-ketothiolase deficiency (3KTD) [MIM:203750]; also known as alpha-methylacetoaceticaciduria. 3KTD is an inborn error of isoleucine catabolism characterized by intermittent ketoacidotic attacks associated with unconsciousness. Some patients die during an attack or are mentally retarded. Urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, triglylglycine, butanone is increased. It seems likely that the severity of this disease correlates better with the environmental or acquired factors than with the ACAT1 genotype.
Belongs to the thiolase family.
Mitochondrion.
Target information above from: UniProt accessionP24752
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry - Anti-ACAT1 antibody [9H10AB4] (ab110290)
![Immunocytochemistry - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-5.gif)
Immunocytochemistry image of ab110290 stained human HDFn cells. The cells were paraformaldehyde fixed (4%, 20 min) and Triton X-100 permeabilized (0.1%, 15 min). The cells were incubated with the antibody (9H10AB4, 5 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) used at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. DAPI was used to stain the cell nuclei (blue). Target protein locates mainly in mitochondria.
Immunoprecipitation - Anti-ACAT1 antibody [9H10AB4] (ab110290)
![Immunoprecipitation - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-6.gif)
ab110290 immunocaptured from HepG2 cells (lane 1) and Human liver mitochondria (lane 2)
Predicted molecular weight is 44 kDa.
Flow Cytometry - Anti-ACAT1 antibody [9H10AB4] (ab110290)
![Flow Cytometry - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-8.gif)
ab110290, at 1 µg/mL, staining ACAT1 in HeLa (blue) or in an isotype control antibody (red) and analyzed by flow cytometry.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ACAT1 antibody [9H10AB4] (ab110290)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-7.gif)
ACAT1 immunohistochemistry in human cerebellum visualized with ab110290. ACAT1 immunoactivity is most intense in neuronal cell bodies, most notably in the large Purkinje cells. Note the distinctive subcellular localization of ACAT1 immunoreactivity in the Purkinje cell bodies. The functional significance of this pattern is unknown at present but this antibody offers the opportunity to investigate it in more detail.
ab110290 has not yet been referenced specifically in any publications.
Publishing research using ab110290? Please let us know so that we can cite the reference in this datasheet
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![Immunocytochemistry - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-5.gif)
Immunocytochemistry image of ab110290 stained human HDFn cells. The cells were paraformaldehyde fixed (4%, 20 min) and Triton X-100 permeabilized (0.1%, 15 min). The cells were incubated with the antibody (9H10AB4, 5 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) used at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. DAPI was used to stain the cell nuclei (blue). Target protein locates mainly in mitochondria.
![Immunoprecipitation - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-6.gif)
ab110290 immunocaptured from HepG2 cells (lane 1) and Human liver mitochondria (lane 2)
Predicted molecular weight is 44 kDa.
![Flow Cytometry - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-8.gif)
ab110290, at 1 µg/mL, staining ACAT1 in HeLa (blue) or in an isotype control antibody (red) and analyzed by flow cytometry.
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ACAT1 antibody [9H10AB4] (ab110290)](/ps/datasheet/images/110/ab110290/ACAT1-Primary-antibodies-ab110290-7.gif)
ACAT1 immunohistochemistry in human cerebellum visualized with ab110290. ACAT1 immunoactivity is most intense in neuronal cell bodies, most notably in the large Purkinje cells. Note the distinctive subcellular localization of ACAT1 immunoreactivity in the Purkinje cell bodies. The functional significance of this pattern is unknown at present but this antibody offers the opportunity to investigate it in more detail.
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