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Read our guarantee »Products:Tags & Cell Markers >> Subcellular Markers >> Cytoskeleton >> Microtubules
Anti-beta Tubulin antibody [TU-06]
See all beta Tubulin products (19) ...
Mouse monoclonal [TU-06] to beta Tubulin
ELISA, WB, ICC, Flow Cytmore details
Reacts with
Mouse, Human, Pig
Predicted to work with
Rat, Chicken, Hamster, Cow, Saccharomyces cerevisiae, Carp, Plants, Schizosaccharomyces pombe
Beta-subunits of tubulin (purified) (Pig).
The antibody TU-06 recognizes the defined epitope (aa 81-95) on phylogenetically conserved N-terminal structural domain of beta tubulin (all charge variants).
Liquid
Store at +4°C. Do not freeze.
Preservative: 15mM Sodium Azide
Constituents: Tris buffered saline, pH 8
Concentration information loading...
Purified IgM
Purified from ascites using precipitation methods. Purity: >95% (by PAGE).
This antibody is one of the only commercial antibodies with the known epitope in the N-terminal domain, a highly conservative structural domain.
Monoclonal
TU-06
IgM
Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Microtubules >> Tubulin
Tags & Cell Markers >> Subcellular Markers >> Cytoskeleton >> Microtubules
Our Abpromise guarantee covers the use of ab7792 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: Use at an assay dependent dilution.
WB: 1/1000
ICC: Use at an assay dependent dilution.
Flow Cyt: Use 1µg for 106 cells.
Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha-chain.
Ubiquitously expressed with highest levels in spleen, thymus and immature brain.
Belongs to the tubulin family.
The highly acidic C-terminal region may bind cations such as calcium.
Some glutamate residues at the C-terminus are polyglutamylated. This modification occurs exclusively on glutamate residues and results in polyglutamate chains on the gamma-carboxyl group. Also monoglycylated but not polyglycylated due to the absence of functional TTLL10 in human. Monoglycylation is mainly limited to tubulin incorporated into axonemes (cilia and flagella) whereas glutamylation is prevalent in neuronal cells, centrioles, axonemes, and the mitotic spindle. Both modifications can coexist on the same protein on adjacent residues, and lowering glycylation levels increases polyglutamylation, and reciprocally. The precise function of such modifications is still unclear but they regulate the assembly and dynamics of axonemal microtubules.
Cytoplasm > cytoskeleton.
Target information above from: UniProt accessionP07437
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - beta Tubulin antibody [TU-06] (ab7792)
![Western blot - beta Tubulin antibody [TU-06] (ab7792)](/ps/datasheet/images/7/ab7792/beta-Tubulin-Primary-antibodies-ab7792-2.jpg)
Anti-beta Tubulin antibody [TU-06] (ab7792) at 1/500 dilution + Human U87 MG whole cell lysate with 5% Milk for 1 hour at 22°C.
Secondary
HRP-conjugated Sheep anti-mouse IgG monoclonal at 1/5000 dilution
This image is courtesy of an anonymous Abreview
Immunocytochemistry/ Immunofluorescence-beta Tubulin antibody [TU-06](ab7792)
](/ps/datasheet/images/7/ab7792/beta-Tubulin-Primary-antibodies-ab7792-3.jpg)
ICC/IF image of ab7792 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab7792, 1æg/ml) overnight at +4øC. The secondary antibody (green)ÿwas Alexa Fluor© 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor© 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43æM.
Flow Cytometry-beta Tubulin antibody [TU-06](ab7792)
](/ps/datasheet/images/7/ab7792/beta-Tubulin-Primary-antibodies-ab7792-4.jpg)
Overlay histogram showing HeLa cells stained with ab7792 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Triton X-100® for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab7792, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgM [ICIGM] (ab91545, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Triton X-100® used under the same conditions.
This product has been referenced in:
See all 8 publications for this product
Publishing research using ab7792? Please let us know so that we can cite the reference in this datasheet
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![Western blot - beta Tubulin antibody [TU-06] (ab7792)](/ps/datasheet/images/7/ab7792/beta-Tubulin-Primary-antibodies-ab7792-2.jpg)
Anti-beta Tubulin antibody [TU-06] (ab7792) at 1/500 dilution + Human U87 MG whole cell lysate with 5% Milk for 1 hour at 22°C.
Secondary
HRP-conjugated Sheep anti-mouse IgG monoclonal at 1/5000 dilution
This image is courtesy of an anonymous Abreview
](/ps/datasheet/images/7/ab7792/beta-Tubulin-Primary-antibodies-ab7792-3.jpg)
ICC/IF image of ab7792 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab7792, 1æg/ml) overnight at +4øC. The secondary antibody (green)ÿwas Alexa Fluor© 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor© 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43æM.
](/ps/datasheet/images/7/ab7792/beta-Tubulin-Primary-antibodies-ab7792-4.jpg)
Overlay histogram showing HeLa cells stained with ab7792 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Triton X-100® for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab7792, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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