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Any news yet on what mouse tissue was used for staining using this antibody? |
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ANSWER: |
Thank you for your email. I followed up with the lab for you, and the in mouse validation for this antibody was performed using NIH3T3 cells. The IHC validation has been done on human tissues. I hope this helps, please let me know if you need any additional information or assistance. |
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Wereally appreciate your cooperation, |
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ANSWER: |
Thank you for confirming these details and for your cooperation. The details provided enable us to closely monitor the quality of our products. |
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Thank you for your response, and I appreciate your cooperation |
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ANSWER: |
Thank you for confirming the details. |
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Thank you for your responce.I attached the questionnaire and an image for the blot. |
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ANSWER: |
Thank you for your email. I am sorry to hear that you are experiencing problems with these antibodies. |
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I am contacting you regarding a purchase we made for antibodies. We bought3 antibodies from Abcam (Mouse monoclonal PR-AT 4.14 to progesterone receptor (ab2764), Mouse monoclonal 33 to estrogen receptor alpha (ab2746) and Rabbit polyclonal to ErbB2 (ab2428)). The ErbB2 ab worked well with us in western blot, while both Abs for ER and PR didn't work. I have tried many times and no band detected inapositive control MCF-7 cell lines. |
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ANSWER: |
Thank you for contacting us. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ab2428 at a 1:200 dilution staining SK-BR-3 whole cell lysate.
Western blot of whole cell lysates of cultured cells, used at a concentration of 1:1000, incubated overnight at 4C, and visualized with an HRP conjugated secondary, with a chemilumenescent detection method. Review by Todd Gocken submitted 20 July 2004
ab2428 staining ErbB 2 in human breast cancer, tissue section by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). Tissue underwent fixation in formaldehyde, heat mediated antigen retrieval in Citrate buffer pH 6.0 and blocking in 10% serum for 1 hour at 20°C.The primary antibody was diluted, 1/100 in TBS and incubated with sample for 12 hours at 4°C. A Biotin conjugated goat polyclonal to rabbit IgG was used undiluted, as secondary. Left hand-side image show staining with ab2428 and developed using DAB detection system while right hand-side shows Isotype control staining with anti-rabbit IgG and DAB.
This image is courtesy of an anonymous Abreview
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