Products:Microbiology >> Organism >> Virus >> DNA Virus >> double stranded DNA Virus >> Other dsDNA viruses
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When this antibody was tested in WB, what was the specific protocol that was used? |
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ANSWER: |
Thank you for your enquiry. This clone was originally characterized in the following publication, Harlow, E., et al. (1981. J. Virol. 39:861, free on-line), the authors originally used this antibody (referred to as L16 in the original publication) to immunoprecipitate 32P-pulsed SV80 cells, then detect the IP by SDS-PAGE, followed by autoradiography. This clone has been characterized for application in Western blotting; however, the exact protocol that was used is not available. We do guarantee that ab16879 will work in Western blotting, and often it is possible to make suggestions that help resolve problems. We will happily offer technical support and in the event that a product is not functioning in the applications cited on the product data sheet (and the problem has been reported within 90 days of purchase), and if it appears that the antibody is at fault, a credit note/refund will be offered. If you would like some technical support I enclose a link to a questionnaire which will help you put your protocol information together very easily so we can look into the details of the experiment and provide some help. http://www.abcam.com/index.html?section=western&pageconfig=technical&intAbID=16879&mode=questionaire |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ab16879 at a 1/50 dilution staining SV40 transfected mouse keratinocytes by ICC/IF.
This image is courtesy of an anonymous Abreview
All lanes : Anti-SV40 T-antigen antibody [PAb416] (ab16879) at 1 µg/ml
Lane 1 : Whole cell lysate mouse embryonic fibroblasts immortalized by transduction with a virus harboring the gene encoding the large T antigen.
Lane 2 : Whole cell lysate mouse embryonic fibroblasts, not immortalized.
Lysates/proteins at 7 µg per lane.
Secondary
HRP conjugated sheep-anti mouse IgG
developed using the ECL technique
Performed under non-reducing conditions.
Predicted band size : 82 kDa
Observed band size : ~80 kDa (why is the actual band size different from the predicted?)
Exposure time : 2 seconds
This image is courtesy of an Abreview submitted by Mr Adam Hoffhines
CV1 cells were either mock infected or infected with SV40 at moi 10. Cells were then harvested (trypsinized and centrifuged) and fixed 72 hours post infection in 100% Methanol at -20°C. Cells were stained for 1 hour with ab16879 at a 1/100 dilution, washed and then stained with Donkey polyclonal Secondary Antibody to Mouse IgG - H&L (DyLight® 488), pre-adsorbed, ab98794 at a 1/200 dilution.
Image courtesy of Nir Drayman by Abreview.
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