This antibody gave a positive signal in HeLa, SHSY-5Y and MALME-3M whole cell lysates, and in the following tissue lysates: Human Cortex, Rat Cortex, Rat Hippocampus, Human Melanoma.
Flow Cytometry: SHSY-5Y cells
保存方法Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C long term.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Drebrin antibody [mAbcam60932] (ab60932)This image is courtesy of an abreview submitted by Carl Hobbs, King's College London, United Kingdom
IHC-P image of mouse SVZ sections showing Drebrin staining using ab60932 (1/2000). The sections were fixed using Formaldehyde. Heat mediated antigen retrieval was performed using citric acid at pH6. The sections were blocked using 1% BSA for 10 mins at 21°C.
Exposure time : 8 minutesAb60932 detects a band around 110-kDa. While this differs to its predicted molecular weight of 71-kDa, it is consistent with what has been described in the literature(PMID:10604653).
Western blot - Drebrin antibody [mAbcam60932] (ab60932)
All lanes : Anti-Drebrin antibody [mAbcam60932] (ab60932) at 10 µg/ml
Lane 1 : Human Cortex Neuronal cell lysate
Lane 2 : Rat Cortex Neuronal cell lysate Lane 3 : Rat Hippocampus Tissue Lysate Lane 4 : Human skin tumor tissue lysate (melanoma) - total protein (ab29339) Lane 5 : Malme 3M (Human melanoma cells) Whole Cell Lysate
Overlay histogram showing SHSY-5Y cells stained with ab60932 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab60932, 1µg/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, 1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in SHSY-5Y cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.