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Could you let me know which region of MMP-3 that ab53015 will detect? |
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ANSWER: |
Thank you for contacting Abcam regarding ab53015. |
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Is ab53015 tested with whole cell lysate or cell conditioned medium? |
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ANSWER: |
Thank you for your call today and for letting us know about the trouble with ab52915. I am sending a free of charge vial of ab53015, on the order ***. I have checked with the production lab, and the lysates used to test this antibody in Western blot were whole 293 cell lysates without any treatment. Please let me know if you have any questions, and keep me updated about the results with ab53015. I look forward to hearing from you. |
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I have ordered the following antibodies, please can you let me know what to dilute them down in ie either PBS or distilled water? Thanking you in advance.Ab 66157- MMP12Ab 51708- IL20Ab 53015 MMP3Ab 58803 MMP9Ab 52631 MMP1 Best wishes |
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ANSWER: |
Thank you for contacting us. We would suggest using PBS with 1% BSA as a diluting buffer. Please be advised that if you would like to store these antibodies at -20 or as recommended on the datasheet then we would recommend storing the antibodies without diluting these. We recommend aliquoting the antibodies in small volumes before storage and using the aliquots as required. I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using MMP3 antibody at a dilution of 1/50. Left: without immunizing peptide; Right: with immunizing peptide.
All lanes : Anti-MMP3 antibody (ab53015) at 1/500 dilution
Lane 1 : Extracts from 293 cells, untreated.
Lane 2 : Extracts from 293 cells, treated with the immunising peptide.
Predicted band size : 54 kDa
Observed band size : 54 kDa
ICC/IF image of ab53015 stained HeLa cells. The cells were 4% formaldehyde 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 (ab53015, 1µg/ml) overnight at +4ºC. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 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.
Top image: Isotype control Middle image: Unstimulated cells Bottom image: IL-1 beta stimulated cells (24 hours, 10 ng/ml)
ab53015 staining MMP3 in Human synovial fibroblasts by Immunocytochemistry/ Immunoflourescence. Cells were fixed in formaldehyde and permeabilized in methanol for 15 minutes at -20°C prior to blocking in 1% BSA for 1 hour at 25ºC. The primary antibody was diluted 1/1000 and incubated with the sample for 2 hours at 25ºC. The secondary antibody was Cy5®-conjugated Goat anti-Rabbit polyclonal, diluted 1/200.
This image is courtesy of an Abreview submitted by Torsten Lowin.
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