Products:Epigenetics and Nuclear Signaling >> DNA methylation >> Methylated DNA
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1 vial (out of 3) with no liquid inside (after centrifugation) - should be 50 ul |
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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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Antibody is not binding in a gel shift or dot blot assay with purchased methyl cytidine DNA. |
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Thank you for your call today and for letting us know about the trouble with ab10805. |
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Dear Tech support |
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Thank you for contacting us. |
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In case the customer has already done 5 ul aliquots, what should he do now? Thank you again, |
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ANSWER: |
Thank you for your recent message. I would suggest performing the experiments, though higher working concentration may be needed to get the expected results. This is mainly due to the fact that smaller aliquots (5 ul) were prepared and no additional protein (i.e. BSA) is added to the storage buffer so a thin film layer may have been formed the internal surface of the tubes and some antibody molecules have adsorbed to it. If you need any further assistance in the future, please do not hesitate to contact me. |
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Is there a problem to store ab10805 in aliquots of 5 ul? Thank you, |
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ANSWER: |
Thank you for your enquiry. Generally, the size of the aliquots will depend on how much one typically uses in an experiment. Aliquots should be no smaller than 10 µl; the smaller the aliquot, the more the stock concentration is affected by evaporation and adsorption of the antibody onto the surface of the storage vial. For further information regarding storage and aliquotting, please visit this site: http://www.abcam.com/index.html?pageconfig=resource&rid=10795 If you need anything further or any help then please let me know. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ab10805 at 1/200 staining mouse bone marrow cells by ICC/IF. The cells were methanol fixed and blocked with BSA before incubation with the antibody for 1 hour. An Alexa Fluor ® 488 conjugated donkey anti-mouse antibody was used as the secondary.
This image is courtesy of an Abreview submitted by Mr Albert Santamaria
ab10805 at 1/200 staining Arabidopsis thaliana root tip meristematic cells by ICC/IF. A Cy3 conjugated sheep polyclonal antibody was used as the secondary.
This image is courtesy of an Abreview submitted by Dr Manuela Silva
ab10805 staining 5-Methyl Cytidine in pig embryo (15 to 17 days) tissue section by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). Tissue underwent fixation in paraformaldehyde, heat mediated antigen retrieval in Tris-EDTA buffer, permeabilization in Triton X-100 and blocking in 2% BSA for 10 minutes at 25°C. The primary antibody was diluted, 1/100 (PBS + 2% BSA) and incubated with sample for 1 hour at 25°C. An Alexa Fluor® 488 conjugated donkey polyclonal to mouse at 1/250 dilution, was used as secondary.
This image is courtesy of an Abreview submitted by Ms Sara Maj Wätjen Hyldig
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