Products:Tags & Cell Markers >> Subcellular Markers >> Nucleus >> Nuclear Envelope
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Phone call requesting information on how to perform WB with Anti-Lamin A + C antibody [131C3] - Nuclear Envelope Marker (ab8984) |
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ANSWER: |
Thank you for calling us and for alerting us to the problem you are experiencing with our product. We take product complaints very seriously, and investigate every product that we feel may not be performing correctly. |
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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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ANSWER: |
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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ANSWER: |
Thank you very much for submitting the Abreview. |
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Sorry for my late response, Im travelling again. |
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Hi, Could you recommend a good antibody that I could use as loading control for western blot on cell membrane fractions? Thanks |
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ANSWER: |
Thank you for your enquiry. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Predicted band size : 70 kDa
A. HT1080 cells + siRNA control sequence
B. HT1080 cells + siRNA Lamin
This picture was submitted by Andrea Robertson as part of a review of ab8984
ab8984 at a 1/200 dilution staining Asynchronous and paraformaldehyde-fixed (4%) HeLa cells by immunocytochemistry. The antibody was incubated with the cells overnight and then detected using a Cy3 conjugated Goat Anti-Mouse IgG (H+L) antibody. The image shows faint, but distinct, nuclear membrane staining.
This image is courtesy of an Abreview by Kirk McManus submitted on 27 February 2006.
All lanes : Anti-Lamin A + C antibody [131C3] - Nuclear Envelope Marker (ab8984) at 1/1000 dilution
Lane 1 : 10ug HeLa whole cell lysate
Lane 2 : 50ug HeLa whole cell lysate
Lane 3 : 100ug HeLa whole cell lysate
Secondary
HRP conjugated goat anti-mouse antibody
developed using the ECL technique
Predicted band size : 70 kDa
Observed band size : 70 kDa
Exposure time : 30 seconds
This image is courtesy of an Abreview submitted by Ms Aarti Jagannath
ab8984 staining dog skeletal muscle tissue cells by ICC/IF. Cells were fixed in methanol and incubated with ab8984, diluted 1/200, for 12 hours at 4°C. A FITC conjugated goat anti-mouse antibody, diluted 1/200, was used as the secondary antibody.
This image is courtesy of an anonymous Abreview
Anti-Lamin A + C antibody [131C3] - Nuclear Envelope Marker (ab8984) at 1/100 dilution + human fibroblast at 15 µl
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 70 kDa
Lysates were prepared in RIPA buffer on ice for 30 min. They were sonicated 4 times for 5 sec prior to mixing with loading buffer.
Overlay histogram showing HeLA cells stained with ab8984 (red line). The cells were fixed with 100% 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 (ab8984, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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