Products:Cell Biology >> Apoptosis >> Nucleus >> Lamins
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ab16375 |
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Our customer is looking for loading control antibody which has over 60kDa size(human sample/WB). She searched ab16048 and please check this is available. |
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Seeing extra bands in western blot that previous lots did not give. |
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ANSWER: |
Thank you for calling Abcam earlier today. |
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I will test the antibody in Vervet monkey cells. Those cells are used in picornavirus studies. I can easily test also our lamin antibodies (lamin A, lamin C and lamin A/C) in those cells. I guess Ill get at least some ab points from those. |
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Off course abpoints will be added to your account whenever you submit a new Abreview. |
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One thing. I just submitted the abreview of ab8981. |
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Thank you very much for submitting the Abreview. |
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Sorry for my late response, Im travelling again. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
All lanes : Anti-Lamin B1 antibody - Nuclear Envelope Marker (ab16048) at 1/1000 dilution
Lane 1 : Hela whole cell lysate
Lane 2 : Hela whole cell lysate with
Lysates/proteins at 20 µg per lane.
Secondary
Alexa fluor goat polyclonal to Rabbit IgG at 1/10000 dilution
Performed under reducing conditions.
Predicted band size : 66 kDa
Observed band size : 68-70 kDa (why is the actual band size different from the predicted?)
ICC/IF image of ab16048 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab16048, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 WGA was used to label plasma membranes (red).
Human and mouse cells stained with ab16048 (1/500). The cells were fixed in 100% methanol for 6 minutes at -20°C, then washed once in PBS.
A: HeLa cells + ab16048 (green)
B: HeLa cells counterstained with DAPI (blue)
C: 3T3 cells + ab16048 (green)
D: 3T3 cells counterstained with DAPI (blue)
Image courtesy of Marilena Ciciarello and Patrizia Lavia, University 'La Sapienza' CNR, Italy
Human and mouse cells stained with ab16048 (1/500). The cells were fixed and permeabilized in 4% formaldehyde, 0.2% Tritonm X100 for 10 minutes at room temperature, then washed 3x in PBS.
A: HeLa cells + ab16048 (green)
B: HeLa cells counterstained with DAPI (blue)
C: 3T3 cells + ab16048 (green)
D: 3T3 cells counterstained with DAPI (blue)
Image courtesy of Marilena Ciciarello and Patrizia Lavia, University 'La Sapienza' CNR, Italy
Anti-Lamin B1 antibody - Nuclear Envelope Marker (ab16048) at 1/1000 dilution + Pancreatic cell line - whole cell lysate at 20 µg
Secondary
HRP conjugated goat anti-rabbit antibody at 1/2000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 66 kDa
Observed band size : 68 kDa (why is the actual band size different from the predicted?)
Exposure time : 30 seconds
This image is courtesy of an anonymous Abreview
IHC image of Lamin B1 staining in human liver FFPE section, performed on a BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab16048, 1µg/ml, for 8 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
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