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Anti-EEA1 antibody [1G11] - Early Endosome Marker
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Mouse monoclonal [1G11] to EEA1 - Early Endosome Marker
ICC/IFmore details
Reacts with
Human
Predicted to work with
Mouse, Rat, Rabbit
Recombinant fragment derived from within residues 50 - 150 of Human EEA1.
This anitbody gave a positive immunofluorescent signal in the following cell lines: HeLa HepG2
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: 0.02% Sodium Azide
Constituents: PBS, pH 7.4
Concentration information loading...
IgG fraction
Monoclonal
1G11
IgG1
Neuroscience >> Neurotransmission >> Intracellular Signaling >> Regulation
Signal Transduction >> Protein Trafficking >> Organelle Proteins
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Endosome
Neuroscience >> Cell Type Marker >> Neuron marker >> Soma marker
Immunocytochemistry/ Immunofluorescence - EEA1 antibody - Early Endosome Marker (ab70521)
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Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)
(enlarge)
Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)
(enlarge)
Our Abpromise guarantee covers the use of ab70521 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 µg/ml
Is unsuitable for or WB.
Binds phospholipid vesicles containing phosphatidylinositol 3-phosphate and participates in endosomal trafficking.
Contains 1 C2H2-type zinc finger.
Contains 1 FYVE-type zinc finger.
The FYVE-type zinc finger domain mediates interactions with phosphatidylinositol 3-phosphate in membranes of early endosomes and penetrates bilayers. The FYVE domain insertion into PtdIns(3)P-enriched membranes is substantially increased in acidic conditions.
Cytoplasm. Early endosome membrane.
Target information above from: UniProt accessionQ15075
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - EEA1 antibody - Early Endosome Marker (ab70521)

ICC/IF image of ab70521 stained HepG2 cells. The cells were fixed with 4% PFA (10 min) and then incubated in 1%BSA / 10% normal Goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70521 at 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 Goat anti-Mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive result in 4% PFA fixed (10 min) HeLa and MCF7 cells at 1µg/ml, and in 100% methanol fixed (5 min) HeLa, HepG2 and MCF7 cells at 5µg/ml.
Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)
![Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)](/ps/datasheet/images/70/ab70521/EEA1-Primary-antibodies-ab70521-6.jpg)
ab70521 staining EEA1 in human THP-1 cells by Immunocytochemistry/ immunofluorescence. Cells were formaldehyde fixed, permeabilized in TritonX100 and blocked in 1% BSA for 1 hour at 25°C. The primary antibody was diluted 1/200 (PBS + Tween20 + BSA 1%) and incubated with sample for 1 hour at 25°C. A 1.4 nm Gold (ultra-small) and Alexa Fluor® 594 conjugated goat polyclonal to mouse IgG1, diluted 1/500 was used as secondary. The red staining in image show EEA1 staining whilst green cytosolic staining corresponds to StarD5.
This image is a courtesy of an anonymous abreview.
Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)
![Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)](/ps/datasheet/images/70/ab70521/EEA1-Primary-antibodies-ab70521-12.jpg)
ICC/IF image of ab70521 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70521, 10µg/ml) overnight at +4°C. The secondary antibody (green) was DyLight® 488 oat anti-mouse IgG - H&L, pre-adsorbed (ab96879) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 15 publications for this product
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ICC/IF image of ab70521 stained HepG2 cells. The cells were fixed with 4% PFA (10 min) and then incubated in 1%BSA / 10% normal Goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70521 at 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 Goat anti-Mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive result in 4% PFA fixed (10 min) HeLa and MCF7 cells at 1µg/ml, and in 100% methanol fixed (5 min) HeLa, HepG2 and MCF7 cells at 5µg/ml.
![Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)](/ps/datasheet/images/70/ab70521/EEA1-Primary-antibodies-ab70521-6.jpg)
ab70521 staining EEA1 in human THP-1 cells by Immunocytochemistry/ immunofluorescence. Cells were formaldehyde fixed, permeabilized in TritonX100 and blocked in 1% BSA for 1 hour at 25°C. The primary antibody was diluted 1/200 (PBS + Tween20 + BSA 1%) and incubated with sample for 1 hour at 25°C. A 1.4 nm Gold (ultra-small) and Alexa Fluor® 594 conjugated goat polyclonal to mouse IgG1, diluted 1/500 was used as secondary. The red staining in image show EEA1 staining whilst green cytosolic staining corresponds to StarD5.
This image is a courtesy of an anonymous abreview.
![Immunocytochemistry/ Immunofluorescence - EEA1 antibody [1G11] - Early Endosome Marker (ab70521)](/ps/datasheet/images/70/ab70521/EEA1-Primary-antibodies-ab70521-12.jpg)
ICC/IF image of ab70521 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70521, 10µg/ml) overnight at +4°C. The secondary antibody (green) was DyLight® 488 oat anti-mouse IgG - H&L, pre-adsorbed (ab96879) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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