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Products:Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Microfilaments >> Talin / Moesin
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Read our guarantee »Anti-Moesin antibody [EP1863Y]
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Rabbit monoclonal [EP1863Y] to Moesin
This antibody reacts with Moesin
IHC-FoFr, WB, IP, ICC, Flow Cyt, IHC-Pmore details
Reacts with
Mouse, Rat, Human
Synthetic peptide corresponding to residues near the C terminus of human Moesin
Human tonsil tissue and Hela cell lysate
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%
Tissue culture supernatant
Monoclonal
EP1863Y
IgG
Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Microfilaments >> Talin / Moesin
Our Abpromise guarantee covers the use of ab52490 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-FoFr: Use at an assay dependent dilution.
WB: 1/1000 - 1/10000. Detects a band of approximately 68 kDa (predicted molecular weight: 68 kDa).
IP: 1/70.
ICC: 1/100 - 1/250.
Flow Cyt: 1/100.
IHC-P: 1/100 - 1/250.
Probably involved in connections of major cytoskeletal structures to the plasma membrane.
In all tissues and cultured cells studied.
Contains 1 FERM domain.
Phosphorylation on Thr-558 is crucial for the formation of microvilli-like structures.
Cell membrane. Cytoplasm > cytoskeleton. Apical cell membrane. Cell projection > microvillus membrane. Phosphorylated form is enriched in microvilli-like structures at apical membrane (By similarity). Increased cell membrane localization of both phosphorylated and non-phosphorylated forms seen after thrombin treatment.
Target information above from: UniProt accessionP26038
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Moesin antibody [EP1863Y] (ab52490)
![Western blot - Moesin antibody [EP1863Y] (ab52490)](/ps/datasheet/Images/52/ab52490/ab52490_1.jpg)
Anti-Moesin antibody [EP1863Y] (ab52490) at 1/100000 dilution + Hela cell lysate at 10 µg
Secondary
Goat anti-rabbit HRP labeled at 1/2000 dilution
Predicted band size : 68 kDa
Observed band size : 68 kDa
Immunohistochemistry (Paraffin-embedded sections) - Moesin antibody [EP1863Y] (ab52490)
![Immunohistochemistry (Paraffin-embedded sections) - Moesin antibody [EP1863Y] (ab52490)](/ps/datasheet/Images/52/ab52490/ab52490_2.jpg)
Immunohistochemical staining of paraffin-embedded human tonsils using ab52490 at a 1/100 dilution.
Flow Cytometry - Moesin antibody [EP1863Y] (ab52490)
![Flow Cytometry - Moesin antibody [EP1863Y] (ab52490)](/ps/datasheet/images/52/ab52490/Moesin-Primary-antibodies-ab52490-2.jpg)
Overlay histogram showing HeLa cells stained with ab52490 (red line). The cells were fixed with 80% 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 (ab52490, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
This product has been referenced in:
See 1 publication for this product
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![Immunohistochemistry (Paraffin-embedded sections) - Moesin antibody [EP1863Y] (ab52490)](/ps/datasheet/Images/52/ab52490/ab52490_2.jpg)
Immunohistochemical staining of paraffin-embedded human tonsils using ab52490 at a 1/100 dilution.
![Flow Cytometry - Moesin antibody [EP1863Y] (ab52490)](/ps/datasheet/images/52/ab52490/Moesin-Primary-antibodies-ab52490-2.jpg)
Overlay histogram showing HeLa cells stained with ab52490 (red line). The cells were fixed with 80% 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 (ab52490, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
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