Products:Cardiovascular >> Angiogenesis >> Growth Factors >> VEGF >> VEGF Receptors
If your product does not perform as described on this datasheet, we will refund or replace your product...
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could you please , let me know what's up with my problem as soon as possible ? |
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ANSWER: |
Thank you once again for taking the time to complete our questionnaire and for your patience. |
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Dear technical support team member , |
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ANSWER: |
Thank you for taking the time to contact us. I am sorry to hear you have had difficulty obtaining satisfactory results from this antibody. |
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I would like to test an anti-neuropilin 1 antibody in zebrafish, an untested species. |
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ANSWER: |
Thank you very much for your interest in ab71945 and ab81321. |
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I am using your np1 ab81321 antibody in wb and getting a band around 130 although your data sheet says 103kDa. Indeed your sample blot does not appear to be at 103kda. Is this a typo? |
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ANSWER: |
Thank you for contacting us. The predicted molecular weight for Neuropilin 1 is 103 kDa, calculated from the amino acid sequence. This protein has numerous glycosylations, each of which will add at least 2 kDa to the observed molecular weight. For this reason, the protein may appear in the range of 120-140 kDa.
For more information about the glycosylation sites or amino acid sequence, please see the UniProt database entry:
http://www.uniprot.org/uniprot/O14786
I hope this helps, please let me know if you need any additional information. |
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I work on NKT cell and recent paper showed nrp1 has some roles in this population. So, I am interested in your product anti-nrp1 monoclonal antibody (ab81321), but not sure for its applicability on FACS. Would you like to provide us a few test dose for this product, then I can purchase it after I confirm its expression? |
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ANSWER: |
Unfortunately we do not have samples of our antibodies to distribute to customers. However, we do guarantee our antibodies to work as we state on the datasheet. We are always happy to help our customers troubleshoot antibody issues. If for any reason you are experiencing problems with an antibody within the first 6 months of your purchase and we are unable to help you troubleshoot them we will be happy to provide you with a free of charge replacement, refund or credit. We have tested this antibody in flow cytometry with mouse, human and rat samples and know the antibody to be working well. I would encourage you to purchase this antibody and use it in your flow cytometry experiments. |
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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-Neuropilin 1 antibody [EPR3113] (ab81321) at 1/1000 dilution
Lane 1 : Human placenta lysate
Lane 2 : HUVEC cell lysate
Lane 3 : HepG2 cell lysate
Lane 4 : mouse heart tissue lysate
Lane 5 : mouse kidney tissue lysate
Lane 6 : rat heart tissue lysate
Lane 7 : rat kidney tissue lysate
Lysates/proteins at 10 µg per lane.
Secondary
HRP goat anti rabbit at 1/2000 dilution
Predicted band size : 103 kDa
Observed band size : 120 kDa (why is the actual band size different from the predicted?)
Immunohistochemical analysis of paraffin-embedded human kidney tissue using ab81321 at 1/100 dilution.
ab81321 staining Neuropilin 1 in Mouse brain tissue sections by Immunohistochemistry (IHC-P - formaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 10% serum for 1 hour at room temperature; antigen retrieval was by heat mediation in citrate buffer (pH 6). Samples were incubated with primary antibody (1/100 in PBS + 2% blocking serum) for 16 hours at 4ºC. A biotin-conjugated Goat anti-rabbit IgG polyclonal (1/250) was used as the secondary antibody.
This image is courtesy of an Abreview submitted by Manoj Kumar Valluru
ab81321 staining Neuropilin 1 in rat brain tissue sections by Immunohistochemistry (frozen sections). Tissue was fixed with paraformaldehyde and then blocked with 10% serum for 1 hour at 27°C followed by incubation with the primary antibody, undiluted, for 14 hours at 4°C. An undiluted Cy3®conjugated donkey anti-rabbit was used as the secondary antibody.
Image courtesy of an anonymous Abreview.
Overlay histogram showing HepG2 cells stained with ab81321 (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 (ab81321, 1/50 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
ICC/IF image of ab81321 stained MCF7 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab81321, 5µg/ml) overnight at +4ºC. The secondary antibody (green) was DyLight® 488 goat anti-rabbit IgG - H&L, pre-adsorbed (ab96899) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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