Mouse Monoclonal Alpha-tubulin 1 acetyl K40 antibody. Suitable for Flow Cyt, WB, IHC-P and reacts with Human samples. Cited in 42 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human TUBA1B acetyl K40.
IgG2b
Mouse
pH: 7.4
Constituents: PBS
Liquid
Monoclonal
Flow Cyt | WB | IHC-P | |
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Human | Tested | Tested | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody. |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
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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.
Tubulin alpha-1B chain, Alpha-tubulin ubiquitous, Tubulin K-alpha-1, Tubulin alpha-ubiquitous chain, TUBA1B
Mouse Monoclonal Alpha-tubulin 1 acetyl K40 antibody. Suitable for Flow Cyt, WB, IHC-P and reacts with Human samples. Cited in 42 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human TUBA1B acetyl K40.
Tubulin alpha-1B chain, Alpha-tubulin ubiquitous, Tubulin K-alpha-1, Tubulin alpha-ubiquitous chain, TUBA1B
IgG2b
Mouse
pH: 7.4
Constituents: PBS
Liquid
Monoclonal
4D1
Tissue culture supernatant
kappa
Purified from TCS.
Blue Ice
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
This product was changed from ascites to tissue culture supernatant on 15 May 2019. Please note that the dilutions may need to be adjusted accordingly. If you have any questions, please do not hesitate to contact our scientific support team.
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Tubulin sometimes called DM1B is a globular protein essential for the formation of microtubules. It has a molecular mass of approximately 55 kDa. Tubulin is expressed in most eukaryotic cells and exists as two closely related subunits alpha-tubulin and beta-tubulin. These subunits polymerize to form linear microtubule structures. Anti-tubulin antibodies such as anti-tubulin Alexa 34 can detect these microtubule markers in cells allowing researchers to visualize cytoskeletal organization.
This core component of microtubule assembly is important for maintaining cell shape enabling intracellular transport and segregating chromosomes during cell division. As part of a complex tubulin interacts with various microtubule-associated proteins (MAPs) that regulate its dynamic assembly and disassembly. This regulation is important for processes like axonal transport in neurons and the movement of cilia and flagella in other cell types.
Tubulin plays a significant role in the mitotic spindle assembly part of the cell cycle. This process is vital for the accurate segregation of chromosomes to daughter cells. Tubulin interacts with the kinesin and dynein motor proteins within this pathway which are essential for intracellular transport and mitosis. Another key pathway involving tubulin is the intracellular trafficking facilitated by motor proteins which is necessary for maintaining cell homeostasis and function.
Aberrant regulation or mutations in tubulin can lead to conditions such as cancer and neurodegenerative diseases. In cancer altered tubulin dynamics contribute to uncontrolled cell proliferation. Neurodegenerative disorders such as Alzheimer’s disease show involvement with tubulin through abnormal microtubule stability often linked to the MAP tau protein. Anti-tubulin antibodies including LAMP1 can help in research related to these conditions by offering methods to study tubulin distribution and function in diseased cells.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Tubulin antibody (ab56676) at 1ug/lane + A-431 cell lysate at 25ug/lane.
This image was generated using the ascites version of the product.
All lanes: Western blot - Anti-Tubulin antibody [4D1] - Loading Control (ab56676)
Predicted band size: 50 kDa
Tubulin antibody (ab56676) used in immunohistochemistry at 3ug/ml on formalin fixed and paraffin embedded human prostate.
This image was generated using the ascites version of the product.
Overlay histogram showing HeLa cells stained with ab56676 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween 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 (ab56676, 2μg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (Goat Anti-Mouse IgG H&L (DyLight® 488) preadsorbed ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2b [PLPV219] (Mouse IgG2b [PLPV219] - Isotype Control ab91366, 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 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
This image was generated using the ascites version of the product.
Blocking Step : 5% BSA for 2 hours at 23°C
This image was generated using the ascites version of the product.
All lanes: Western blot - Anti-Tubulin antibody [4D1] - Loading Control (ab56676) at 1 µg/mL
Lane 1: Whole tissue lysate of rabbit heart at 20 µg
Lane 2: Whole tissue lysate of rabbit heart at 40 µg
Lane 3: Whole tissue lysate of rabbit heart at 60 µg
Lane 4: Whole tissue lysate of rabbit heart at 80 µg
Lane 5: Whole tissue lysate of rabbit heart at 100 µg
Lane 6: Whole tissue lysate of rabbit heart at 120 µg
All lanes: An HRP-conjugated Donkey anti-mouse IgG polyclonal at 1/50000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 50 kDa
Observed band size: 47 kDa
Exposure time: 1s
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