Products:Neuroscience >> Cell Type Marker >> Neural Stem Cell marker
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Can you tell me which part of the protein this antibody was raised against? Was it the cytoplasmic or extracellular domain? |
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ANSWER: |
Unfortunately we do not have any any other information about the portion of the protein that this antibody was raised against. |
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I had a question about the differences between ab3167 an ab35. From a glance these antibodies look extremely similar. For ab3167, it seems like an enzyme-based antigen retrieval method is recommended while citrate buffer is used for ab35. Is this the main difference? I am interested in using the antibody on paraffin-embedded sections. Has this antibody been previously tested on bladder sections? Thanks for your help.
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ANSWER: |
Thank you for your enquiry. Both ab35 and ab3167 have been tested and shown to work using immunohistochemistry on paraffin sections. You are correct that these antibodies do indeed seem similar. Indeed because the clone numbers; [4B7] and [4B7R] are so similar I suspect that [4B7R] maybe a derivative of the other. However, the preparation of the antibody is likely to be different. This is reflected in the differences that you have highlighted in the antigen retrieval method. Unfortunately I do not have details of either of these antibodies being tested on bladder sections. However, we guarantee both of them to work by immunohistochemistry on paraffin sections. I hope this information helps, please do not hesitate to contact us if you need any more advice or information. |
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Customer would like to know: what end of the integrin was the antibody raised against? |
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ANSWER: |
Thank you for your phone call. I regret to inform you that concerning the antibodies that you are interested in, we do not have any information regarding the epitopes. If you have any more questions, please contact us again. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Image courtesy of Human Protein Atlas
ab3167 staining Integrin beta 1 in Human skin, showing a distinct and strong staining pattern at the basal cells of the squamous epithelium that contrasts with the reticular layer. Paraffin embedded human skin tissue was incubated with ab3167 (1/35 dilution) for 30 mins at room temperature. Antigen retrieval was performed by heat induction in citrate buffer pH 6.
ab3167 was tested in a tissue microarray (TMA) containing a wide range of normal and cancer tissues as well as a cell microarray consisting of a range of commonly used, well characterised human cell lines. Further results for this antibody can be found at www.proteinatlas.org
Anti-Integrin beta 1 antibody [4B7R] (ab3167) at 5 µg/ml + HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate at 10 µg
Secondary
Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
Predicted band size : 88 kDa
Observed band size : 100 kDa (why is the actual band size different from the predicted?)
Additional bands at : 37 kDa,40 kDa,50 kDa. We are unsure as to the identity of these extra bands.
It is probable that this protein runs higher than the predicted MW as it likely to be glycosylated.
Overlay histogram showing MCF-7 cells stained with ab3167 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab3167, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
Please note that Abcam do not have data for use of this antibody on non-fixed cells. We welcome any customer feedback.
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