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We found the expiry date given below was not written on the antibody labels. The customers are querying about this and I would like to have some letter mentioning the expiry dates of these two items. Thank you. |
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ANSWER: |
Thank you for your enquiry. The antibody storage conditions are detailed on every datasheet under the "Storage instructions" section. We make the general recommend that should our antibodies stipulate storage at -20oC then they can be stored for up to 2 years at this temperature. Likewise we suggest that our antibodies can be stored at -80oC for 10 years. When an antibody can only be kept at 4oC we recommend that it is functional for up to 12 months. I hope this information helps, please do not hesitate to contact us if you need any more advice or information. |
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ReviewID: 4120 AbID: 2712 Status: Submitted TIA1 antibody [TIA-1] (ab2712): Sample: Human Cell (HeLa) Application: Immunocytochemistry/Immunofluorescence Blocking step:: Serum as blocking agent for 0 hour(s) 15 minute(s) Concentration: 1% Fixation:: Paraformaldehyde Antigen retrieval step:: None Incubation time:: 1 hour(s) 0 minute(s) Positive control:: My samples Dilution: 1/100 Rating: Didn't work - I would not use it again Secondary antibody: Name:: Non-Abcam one was used: [competitor] Conjugation: Cy3 Dilution:: 1/500 |
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ANSWER: |
Thank you for taking the time to submit a review to our system. I am taking your comments seriously and would appreciate your assistance to enable me to look into the source of the problem in more detail. Could you fill out the questionnaire at the following link so I can examine the details of your protocol more closely? http://www.abcam.com/index.html?section=ihc&pageconfig=technical&intAbID=2712&mode=questionaire My first recommendation would be to try Anaplastic large cell lymphoma or tonsil as a positive control as stated on our datasheet. I noticed that you fixed with 4% paraformaldehyde, however, we do know with formalin fixation that you need to use antigen retrieval and since this is an intracellular protein that you will need to use a permeabilization. I would recommend permeabilizing with 0.25% Triton X-100 or 100 uM digitonin or 0.5% saponin or trying an alternative fixative such as acetone. I hope this information helps you and I look forward to receiving your reply. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ab2712 at 1/3300 dilution staining monkey COS 7 cells by ICC/IF. The cells were cultured for 2 hours at 45oC and fixed in cold Methanol: Acetone 1:1 for 10 minutes. The TIA1 antibody was directly conjugated with Alexa Fluor ® 568 and after 1 hour incubation a second fixation step was performed.
This image is courtesy of an Abreview submitted by Mrs Gabriela Elena Oprea
Human normal spleen. Staining is observed in the cytoplasm. Left panel: with primary antibody at 1 ug/ml. Right panel: isotype control. Sections were stained using an automated system DAKO Autostainer Plus , at room temperature: sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffers citrate EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for mouse for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
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