Products:Tags & Cell Markers >> Subcellular Markers >> Cytoskeleton >> Microtubules
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Could you, please, help me with making a right choice of anti-alpha tubulin antibody. I need to make double immunostainings in Drosophila S2 cells to visualize co-localisation of the protein of my interest with mitotic spindle in dividing cells. I found that anti-alpha-tubulin antibody is mostly used for visualizing microtubules. For my application I need anti-alpha tubulin antibody produced in rabbit. In Abcam catalog I found only one antibody ab15246 that is indicated to recognize Dm antigen. But the datasheet for this product is lacking indication on how to use this antibody for fluorescent immunostainings. The PubMed reference 17785506 provided contains no details on that question either. On the other hand datasheet for antibody ab18251 contains an Abreview where this antibody was successfully used for immunostaining Drosophila embryos as well as details on antibody dilution. But in the datasheet itself it's not indicated that ab18251 reacts with Dm. So which antibody I should order to bring my experiment to success? |
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ANSWER: |
Thank you for contacting us.
We would guarantee both ab15246 and ab18251 to stain cells from drosophila via immunocytochemistry (ICC/IF). I am not sure why drosophila wasn't added as a tested species to the datasheet for ab18251 after that Abreview was added, but this was an oversight and I have since updated the datasheet to include drosophila as a tested species.
As for the references for ab1546, we know of them testing drosophila by WB and IHC-Fr, not ICC/IF, per se. But we would still guarantee the antibody to work in drosophila and ICC/IF since both the species and application were tested, although independently.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048163/pdf/cm0068-0001.pdf
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2562427/pdf/nihms70131.pdf
If you're looking for an ICC/IF protocol to use with ab1546, you can look at the below two articles, tested in mouse and human, and just apply that same protocol to your cells from drosophila.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872425/pdf/pnas.200910941.pdf
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2851247/pdf/nihms120363.pdf
Both of these antibodies would be covered under our Abpromise to use them with drosophila in ICC/IF so if you ran into any difficulty, we would be happy to replace or refund them for you within 6 months of your purchase.
I hope this information is helpful to you. 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"
ICC/IF image of ab18251 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab18251, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue).
All lanes : Anti-alpha Tubulin antibody (ab18251) at 0.5 µg/ml
Lane 1 : HeLa lysate
Lane 2 : A431 lysate
Lysates/proteins at 20 µg per lane.
Secondary
Alexa Flour Goat polyclonal to Rabbit IgG (700) at 1/10000 dilution
Predicted band size : 50 kDa
Observed band size : 50 kDa
Additional bands at : 30 kDa (possible cross reactivity).
ab18251 detects a strong band at 50 kDa corresponding to alpha tubulin. Cross-reactivity is also seen with other lower molecular weight bands. This may be reduced by using the antibody at a lower working concentration.
ab18251 at a 1/8000 dilution staining human HeLa cells by immunocytochemistry. The cells were paraformaldehyde fixed and incubated with the antibody for 30 minutes. The secondary antibody was a Cy3 conjugated Goat Anti-Rabbit IgG (H+L). The image shows staining of an interphase IM cell.
This image is courtesy of an Abreview by Kirk McManus submitted on 27 February 2006.
Image courtesy of Human Protein Atlas
ab18251 staining alpha Tubulin. Paraffin embedded human appendix tissue was incubated with ab18251 (1/2500 dilution) for 30 mins at room temperature. Antigen retrieval was performed by heat induction in citrate buffer pH 6. ab18251 was tested in a tissue microarray (TMA) containing a wide range of normal and cancer tissues as well as a cell microarray consisting of a range of commonly used, well characterised human cell lines.
Further results for this antibody can be found at www.proteinatlas.org
ab18251 staining alpha Tubulin in HeLa cells by Immunocytochemistry/ Immunofluorescence.ab18251 staining alpha Tubulin labeled red.ab20740 staining Lamin A labeled green.Hoechst 33258 staining DNA blue.
Image from Mackay DR et al, J Cell Biol. 2010 Nov 29;191(5):923-31. Epub 2010 Nov 22, Fig 1. DOI 10.1083/jcb.201007124
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