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IHC-P with mouse retina |
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Thank you for contacting us. |
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Brown, stringy, lint on tissue sections stained at higher concentration with this antibody. |
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Thank you for your call yesterday, and I'm sorry to hear that the replacement vial of ab2426 has also given the same problem. |
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I am forwarding this email from the beginning of September where we had some issues with the PCNA antibody ab2426. We sent pictures to you back then of the problem and we do thank you for replacing the lot. Unfortunately it is now 6 months later and this new lot that was sent to replace the first is having the same exact brown stringy problem. This is the only antibody that I have ever seen this occur with..and we work with A LOT of different antibodies from many many companies. Could you please help us with what is going on with this antibody. This antibody is so great with it's staining and we have such a great protocol for it but our entire experiments get ruined because we can not take publication quality images of our tissue with all of this brown stringy mess all over each tissue piece with PCNA on it. |
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Thank you for your reply and for keeping me updated about this situation. I'm sorry to see that the results with the replacement vial were also unsatisfactory. |
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Please let us know if you can provide any offer if we use the following on Shark samples: |
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Thank you very much for your interest in our antibodies and kits. |
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I would like to test ab2426 for IHC-P canine tissue. |
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DISCOUNT CODE: ********* |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Ab2426 was used for immunohistochemistry, at a 1:500 dilution in hamster neural tissue, identified with a polyclonal secondary and DAB detection kit. Review by Kevin Bath submitted 18 June 2004
ab2426 at 1/200 dilution staining rat skeletal muscle satellite stem cells by ICC/IF.
Cultured rat skeletal muscle satellite stem cells (SKMB) were 2% paraformaldehyde fixed for 15 minutes and then permealized with Triton-X100 prior to incubation with ab2426 overnight at 4°C. An Alexa-Fluor ® 488 conjugated donkey anti-rabbit antibody was used as the secondary.The image shows DAPI (blue-nuclear stain, upper left panel), PCNA (Green, upper right panel, showing nuclear localization in actively dividing cells), same SKMB cells -DIC (phase) image (lower left panel) and superimpose fluorescence image (lower right panel).
This image is courtesy of an Abreview submitted by Dr Mal Niladri
All lanes : Anti-PCNA antibody - Proliferation Marker (ab2426) at 1/200 dilution
Lane 1 : HeLa (Human epithelial carcinoma cell line) Nuclear Lysate
Lane 2 : HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate
Lysates/proteins at 20 µg per lane.
Secondary
IRDye 680 conjugated Goat anti-rabbit IgG (H&L) at 1/15000 dilution
Predicted band size : 29 kDa
Observed band size : 29 kDa
ab2426 staining PCNA in murine skin tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). Tissue was fixed with formaldehyde and a heat mediated antigen retrieval step was performed using TRIS EDTA pH 8.2. Samples were then incubated with the primary antibody at a 1/2000 dilution for 1 hour at 37ºC. An undiluted HRP-conjugated rabbit polyclonal was used as secondary antibody.
Image courtesy of Laurence Sifre by Abreview.
ab2426 staining PCNA in murine epithelial tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections).Wound tissue sections (0.5 µm) were cut using a microtome and collected on slides. Sections were then de-waxed in xylene and rehydrated by successive immersion in descending concentrations of alcohol. The sections were then subjected for immunofluorescence staining. Briefly, tissue sections were blocked by incubated with 5% donkey serum for 1 hour and washed with phosphate-buffered saline (PBS). Sections were then incubated with ab2426 at a 1/500 for 1 hour at room temperature under humidified conditions. After primary antibody incubation, sections were washed with PBS and incubated with appropriate fluorescent secondary antibodies for 1 hour at room temperature. Sections were then washed with PBS, mounted with mounting medium containing DAPI.
Image from Liu S et al, J Cell Sci. 2010 Nov 1;123(Pt 21):3674-82. Epub 2010 Oct 12, Fig 3. DOI 10.1242/?jcs.070672
All lanes : Anti-PCNA antibody - Proliferation Marker (ab2426) at 1/300 dilution
Lane 1 : Whole tissue lysate prepared from mouse heart
Lane 2 : Whole tissue lysate prepared from mouse heart
Lane 3 : Whole tissue lysate prepared from mouse heart
Lane 4 : Whole tissue lysate prepared from mouse heart
Lysates/proteins at 50 µg per lane.
Secondary
HRP-conjugated pig anti-rabbit polyclonal at 1/3000 dilution
developed using the ECL technique
Predicted band size : 29 kDa
Observed band size : 29 kDa
Exposure time : 2 minutes
Image courtesy of an anonymous Abreview.
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