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Read our guarantee »Products:Neuroscience >> Cell Type Marker >> Glia marker >> Astrocyte marker
Anti-ABCA1 antibody [AB.H10]
See all ABCA1 products (11) ...
Mouse monoclonal [AB.H10] to ABCA1
IHC-P, ICC/IF, Flow Cyt, WB, ELISA, IPmore details
Reacts with
Mouse, Rat, Chicken, Cow, Human
Recombinant fragment, corresponding to amino acids 1800-2260 of Human ABCA1.
testis, liver, and brain tissue (negative control: muscle tissue)
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: PBS, pH 7.4
Concentration information loading...
IgG fraction
Monoclonal
AB.H10
IgG1
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of lipids and lipoproteins
Cardiovascular >> Atherosclerosis >> Lipoprotein metabolism
Signal Transduction >> Metabolism >> Lipid metabolism
Cardiovascular >> Lipids / Lipoproteins >> Lipid Metabolism >> Cholesterol Metabolism
Neuroscience >> Cell Type Marker >> Glia marker >> Astrocyte marker
Our Abpromise guarantee covers the use of ab18180 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: 1/200Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
ICC/IF: Use at an assay dependent concentration.
Flow Cyt: Use 1-2µg for 106 cells.
WB: 1/1000Predicted molecular weight: 254 kDa.
ELISA: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
cAMP-dependent and sulfonylurea-sensitive anion transporter. Key gatekeeper influencing intracellular cholesterol transport.
Widely expressed, but most abundant in macrophages.
Defects in ABCA1 are a cause of high density lipoprotein deficiency type 1 (HDLD1) [MIM:205400]; also known as analphalipoproteinemia or Tangier disease (TGD). HDLD1 is a recessive disorder characterized by absence of high density lipoprotein (HDL) cholesterol from plasma, accumulation of cholesteryl esters, premature coronary artery disease (CAD), hepatosplenomegaly, recurrent peripheral neuropathy and progressive muscle wasting and weakness.
Defects in ABCA1 are a cause of high density lipoprotein deficiency type 2 (HDLD2) [MIM:604091]; also known as familial hypoalphalipoproteinemia (FHA). HDLD2 is inherited as autosomal dominant trait. It is characterized by moderately low HDL cholesterol, predilection toward premature coronary artery disease (CAD) and a reduction in cellular cholesterol efflux.
Belongs to the ABC transporter superfamily. ABCA family.
Contains 2 ABC transporter domains.
Multifunctional polypeptide with two homologous halves, each containing an hydrophobic membrane-anchoring domain and an ATP binding cassette (ABC) domain.
Phosphorylation on Ser-2054 regulates phospholipid efflux.
Palmitoylation by DHHC8 is essential for membrane localization.
Membrane.
Target information above from: UniProt accessionO95477
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Anti-ABCA1 antibody [AB.H10] (ab18180)
![Western blot - Anti-ABCA1 antibody [AB.H10] (ab18180)](/ps/datasheet/Images/18/ab18180/ab18180_1.jpg)
Predicted band size : 254 kDa
Western blot analysis of ABCA1 induction by cholesterol (+) in human fibroblast cells from different patients (1,2,3,4). Simultaneous blotting with anti-actin antibody was used for protein loading control.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - ABCA1 antibody [AB.H10] (ab18180)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - ABCA1 antibody [AB.H10] (ab18180)](/ps/datasheet/Images/18/ab18180/ab18180_2.jpg)
Immunoreactivity of pancreas tissue for ABCA1 protein. Left panel: strong immunopositivity of exocrine glandular cells of the pancreas, especially in the basal region (arrows). Interstitial microvascular cells are apparently negative. Cells within the islet were weakly positive (data not shown). Right panel: the negative control. Hematoxylin counterstain.
Flow Cytometry - ABCA1 antibody [AB.H10] (ab18180)
![Flow Cytometry - ABCA1 antibody [AB.H10] (ab18180)](/ps/datasheet/images/18/ab18180/ABCA1-Primary-antibodies-ab18180-11.jpg)
Overlay histogram showing HepG2 cells stained with ab18180 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab18180, 2µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HepG2 cells fixed with 4% paraformaldehyde/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 17 publications for this product
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![Western blot - Anti-ABCA1 antibody [AB.H10] (ab18180)](/ps/datasheet/Images/18/ab18180/ab18180_1.jpg)
Predicted band size : 254 kDa
Western blot analysis of ABCA1 induction by cholesterol (+) in human fibroblast cells from different patients (1,2,3,4). Simultaneous blotting with anti-actin antibody was used for protein loading control.
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - ABCA1 antibody [AB.H10] (ab18180)](/ps/datasheet/Images/18/ab18180/ab18180_2.jpg)
Immunoreactivity of pancreas tissue for ABCA1 protein. Left panel: strong immunopositivity of exocrine glandular cells of the pancreas, especially in the basal region (arrows). Interstitial microvascular cells are apparently negative. Cells within the islet were weakly positive (data not shown). Right panel: the negative control. Hematoxylin counterstain.
![Flow Cytometry - ABCA1 antibody [AB.H10] (ab18180)](/ps/datasheet/images/18/ab18180/ABCA1-Primary-antibodies-ab18180-11.jpg)
Overlay histogram showing HepG2 cells stained with ab18180 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab18180, 2µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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