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ab14960 |
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Customer bought Nanog antibody and would like an isotype control. Staining on ES cells. |
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ANSWER: |
Thank you for your enquiry. There are at least three isotype controls you could use: normal rabbit serum (ab7487), ab27472, ab27478. I hope this information helps, please do not hesitate to contact us if you need any more advice or information. |
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What is the homology of your abs to bovine nanog (DQ069776)? |
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ANSWER: |
Thank you for your enquiry and your patience in waiting for my reply. I have compared the immunogen sequences with the sequence of bovine nanog using a ClustalW alignment. For ab14959 less than 30% of the sequence is homologous, for ab21624 the homology is 50%, and for ab21603 the epitope is not known but the overall sequence homology is approximately 50%. The end result in my opinion is that the homology is not high enough for any of these antibodies to cross-react with bovine nanog. You would want to see a higher degree of homology to have any confidence that these antibodies would cross-react with bovine nanog. I hope this information helps, 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"
Lanes 1-4 : Nanog antibody (ab14959) at 1 ug/ml
Lanes 3-4 : Nanog peptide (ab14960) at 1 ug/ml
Observed band size: 34.2 kDa
Additional bands at: 18 kDa (possible cross reactivity), 38 kDa (possible cross reactivity), 50 kDa (possible cross reactivity).
Lanes 1 and 3: Mouse embryonic stem cell lysate (positive control)
Lanes 2 and 4: Human embryonic stem cell lysate (negative control)
ab14959 recognised a band of the expected size for Nanog in mouse embryonic stem cells but not in human embryonic stem cells. Additional bands were also recognised in mouse embyonic stem cells.
Performed under reducing conditions.
All lanes : Anti-Nanog antibody (ab14959) at 0.8 µg/ml
Lane 1 : ES Cell Nuclear Extract
Lane 2 : ES Cell Nuclear Extract
Predicted band size : 34 kDa
Adam Yates and Ian Chambers, University of Edinburgh
ab14959 staining mouse teratoma sections by IHC-P. The tissue was fixed with formaldehyde and a heat mediated antigen retrival step was performed with citric acid pH 6. Blocking of the sample was done with 1% BSA for 10 minutes at 21°C, followed by staining with ab14959 at 1/600 in TBS/BSA/azide for 2h at 21°C. A biotinylated goat anti-rabbit polyclonal antibody at 1/200 was used as the secondary antibody.
This image is courtesy of an Abreview submitted by Carl Hobbs
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