Products:Neuroscience >> Neurology process >> Growth and Development >> Axonal Guidance Proteins
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ab88818 |
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Abreview testing codes have expires prematurely. |
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ANSWER: |
Thank you for your call today, and I apologize for the trouble with these codes! I have created new codes which will expire on March 1, 2012. I will go through your Abreviews and put these new codes in our internal notes so that the discounts can be applied to your orders tomorrow. Please let me know if you have any questions, or if there is anything else that we can do for you. |
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I received an inquiry about your product, ab23393; Semaphorin3A antibody. The customer told us that this antibody was used for immunofluorescent staining on acetone-fixed cryosections in the below reference. PMID: 16330548 J Biol Chem. 2006 Feb 3;281(5):2721-9. Epub 2005 Dec 5. Could you guarantee an application of this antibody for IF? |
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ANSWER: |
Thank you for your enquiry. I appreciate you highlighting this publication to me. I have added it to the antibody datasheet in addition to the application of IHC using frozen sections. Yes, we would guarantee this antibody to work by this application with all future purchases of this antibody. Thank you once again. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Lanes 1 - 2 : Anti-Semaphorin 3A antibody (ab23393) at 1/1000 dilution
Lanes 3 - 4 : Anti-Semaphorin 3A antibody (ab25999)
Lane 1 : Neonatal rat brain
Lane 2 : Human recombinant Sema3A/Fc chimera (95/125 kDa)
Lane 3 : Neonatal rat brain
Lane 4 : Human recombinant Sema3A/Fc chimera (95/125 kDa)
Predicted band size : 89 kDa
Membrane was incubated with diluted antibody in 5% non-fat milk, PBS, 0.04% Tween20 for 1hour at room temperature.
Ab23393 staining human normal ileum. Staining is localized to 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 buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS), then incubated with primary antibody for 20 minutes, and detected with Dako Envision Flex amplification kit 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.
Anti-Semaphorin 3A antibody (ab23393) at 1/1000 dilution + Lysate prepared from Xenopus laevis brain tissue section at 15 µg
Secondary
HRP-conjugated goat polyclonal to rabbit IgG at 1/20000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 89 kDa
Observed band size : 106 kDa (why is the actual band size different from the predicted?)
Additional bands at : 65 kDa. We are unsure as to the identity of these extra bands.
Exposure time : 1 minute
This image is a courtesy of Anonymous Abreview
ab23393 staining Semaphorin 3A in 16 µm thick sections of Apteronotus leptorhynchus brain, spinal cord by Immunohistochemistry (Frozen sections).Tissue was fixed in 2% paraformaldehyde, permeabilized using 0.3% Triton X-100, then blocked with 3% sheep serum, 1% BSA, 1% teleostean gelatine in TBS for 1 hour at 24°C and then incubated with ab23393 at a 1/50 dilution for 18 hours at 4°C. The secondary used was an Alexa-Fluor 488 conjugated goat anti-rabbit polyclonal used at a 1/200 dilution.
Image courtesy of Dr Ruxandra Sirbulescu by Abreview.
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