Anti-Apolipoprotein M antibody [8F12C6B8]
| Name | Anti-Apolipoprotein M antibody [8F12C6B8] |
|---|---|
| Supplier | Abcam |
| Catalog | ab66379 |
| Prices | $370.00 |
| Sizes | 100 µg |
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG1 |
| Clone | 8F12C6B8 |
| Applications | FC WB ELISA ICC/IF ICC/IF |
| Species Reactivities | Human |
| Antigen | Ni-NTA purified full-length recombinant Apolipoprotein M expressed in E |
| Description | Mouse Monoclonal |
| Gene | APOM |
| Conjugate | Unconjugated |
| Supplier Page | Shop |
Product images
![All lanes : Anti-Apolipoprotein M antibody [8F12C6B8] (ab66379) at 1/500 dilutionLane 1 : human serumLane 2 : human serumLane 3 : human serum](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_1/8636_66379wb.jpg)
All lanes : Anti-Apolipoprotein M antibody [8F12C6B8] (ab66379) at 1/500 dilutionLane 1 : human serumLane 2 : human serumLane 3 : human serum
Immunofluorescnece analysis of COS-7 cells using ab66739 at a dilution of 1/200 - 1/1000, showing cytomembrane localization.
Immunofluorescnece analysis of L-02 cells using ab66739 at a dilution of 1/200 - 1/1000, showing cytomembrane localization.
![Overlay histogram showing HepG2 cells stained with ab66379 (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 (ab66379, 2µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. 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.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_1/8639_Apolipoprotein-M-Primary-antibodies-ab66379-1.jpg)
Overlay histogram showing HepG2 cells stained with ab66379 (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 (ab66379, 2µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. 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.