Products:Tags & Cell Markers >> Cell Type Markers >> Tumor Associated
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Thank you for your kind help. So after this conversation, I can understand that I can use your HRP kit for the labeling for the secondary antibody. In that case there is no need to use tertiary antibody. |
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ANSWER: |
Thank you for your email. |
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Thank you for your kind reply. Can your HRP conjugation kit (ab102891) be able to solve the above problems which may arise during the use of other company's HRP kit? |
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ANSWER: |
The conjugation kit ab102891 is compatible with antibody formulations that contain up to 1% BSA, even though the BSA is in 10-fold excess to the antibody (10mg/ml BSA compared to 1 mg/ml IgG for ab71720). Some of the BSA will itself will be conjugated, affecting efficient conjugation of the IgG, so an antibody without BSA would be better, such as anti-PSMA ab19071. |
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Thank you very much for your kind reply. Is it necessary to use 3rd labeled antibody? |
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ANSWER: |
I think the CEA antibody formulation will be compatible with the other company's labeling kit but you should contact them and send them the buffer components. Here are the components of the ab15987 buffer: |
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Thanks for the reply. |
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ANSWER: |
Thank you for your resposne. |
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Dear technical team, |
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ANSWER: |
Thank you for your enquiry. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Standard Curve for Carcino Embryonic Antigen CEA dilution range 1pg/ml to 1ug/ml using Capture Antibody Mouse monoclonal [26/3/13] to Carcino Embryonic Antigen CEA (ab4451) at 0.2ug/ml and Detector Antibody Rabbit polyclonal to Carcino Embryonic Antigen CEA (ab15987) at 0.5ug/ml
ICC/IF image of ab15987 stained HepG2 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 (ab15987, 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.
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