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ab46666 |
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The immunogen says, "His-tagged Kaiso fusion protein (Human) lacking the zinc finger region." Do you have the actual residues? According to Swiss Prot, the region of a.a. 514 - 638 is required for DNA binding. Does this work in ChIP because this region is included in the immunogen? |
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ANSWER: |
Thank you for your inquiry. I heard back from our lab that unfortunately we do not have any more information on the immunogen sequence other than what is stated on the datasheet. Ideally, for an antibody that works in ChIP, the immunogen sequence should avoid the DNA binding domain. This is because if the target protein has bound to the DNA, this region is now blocked and no longer accessible to the antibody. For this reason we also try to avoid designing immunogens to the activation domain too. I hope this information helps. Please contact us with any other questions. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Immunofluorescence using clone 6F / 6F8 on C2C12 cells.
Predicted band size : 80 kDa
Kaiso was IP'd from CSML0 cells using clone 6F / 6F8 and western blotted using clone 6F / 6F8.
Overlay histogram showing HeLa cells stained with ab12723 (red line). The cells were fixed with 80% methanol (5 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 (ab12723, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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