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dear Sir, |
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ANSWER: |
Thank you for contacting us. |
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I am interested in some of your products. I wonder if the Anti-CD47 antibody[B6H12.2](ab3283) and Anti-HLA Class 1 ABC antibody [EMR8-5] (ab70328) crossreact with cynomolgus monkeys. If they crossreact with monkeys, could you recommend any antibody which is specific for human but doesn't crossreact with cynomolgus monkeys? Thank you very much! |
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Thank you for contacting Abcam. |
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We are planning to do some CD47-measurements with to different antibody-clones, that mustn't compete for the same CD47-binding site, but both habe to bind the protein at the same time. Up to now we couldn't find any information about the epitope specifity of commerzialized anti-CD47 antibodies. We'd be very pleased if you could possibly provide some further information concerning this issue.
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ANSWER: |
Thank you for your enquiry. For ab3283, the information that we regarding the epitope is that it is the Ig domain. For ab9089, the epitope has not yet been mapped. If you have any more questions, please contact us again. |
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We are interested in working with your product CD47 antibody [B6H12.2] or CD47 antibody [MEM-122]. According to your data sheets and the literature they work well with primate cells. Since we use mouse cells, however, we would like to know whether you have any additional data about the specificity of the antibodies. If not, would it be possible for you to provide us a small aliqout for testing the reactivity on material derived from mice?
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ANSWER: |
Thank you for your enquiry. All the information we have on species cross reactivity is specified on the datasheet. To our knowledge, cross reactivity with mouse has not yet been tested. We do not routinely offer free or trial sized samples for testing purposes. Our policy at Abcam is that if an antibody does not work as specified on the datasheet, we will offer a replacement or reimbursement. Should you decide to test an antibody in an application for which we do not have any information, please let us know how you get on and in return we will forward a GBP10/ USD15/ EUR15 Amazon gift voucher. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ab3283 staining CD47 in HUVEC cells by Immunocytochemistry/ Immunofluorescence.The cells were fixed with 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.25% Triton X-100 for 5 minutes and blocked with 1% BSA in 0.1% Tween 20 and PBS for 1 hour at room temperature. The cells were incubated in a mixture of two primary antibodies ab3283 and a rabbit anti-human VEGFR2 overnight at 4 ºC. The cells were then incubated with a mixture of two secondary antibodies (Alexa Fluor 488 anti-rabbit and Alexa Fluor 594 anti-mouse) in 1% BSA for 1 hour at room temperature in the dark. Counterstained with DAPI.
Image from Kaur S et al, J Biol Chem. 2010 Dec 10;285(50):38923-32. Epub 2010 Oct 5, Fig 5.
ab3283 at 1µg/ml staining CD47 from human OVCA3 cells by ICC. The cells were methanol fixed, blocked with 3% serum and incubated with the primary antibody for 30 minutes. A biotinylated horse anti-mouse IgG was used as the secondary antibody.
This image is courtesy of an Abreview submitted by Mr Benjamin Misemer
Anti-CD47 antibody [B6H12.2] (ab3283) at 1 µg/ml +
Secondary
Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 35 kDa
Observed band size : 49 kDa (why is the actual band size different from the predicted?)
Exposure time : 4 minutes
CD47 contains an exstensive number of potential glycosylation sites (SwissProt) which may explain its migration at a higher molecular weight than predicted.
Overlay histogram showing peripheral blood lymphocytes stained with ab3283 (red line). The cells were incubated with the antibody (ab3283, 1µg/1x106 cells) for 30 min at 4ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H&L) (
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