For immunochemical detection of detyrosinated α-tubulin
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Detyrosinated α-Tubulin Rabbit Monoclonal Antibody (Clone RM444)

Item No. 35807

Technical Information
Synonyms
  • Glu-tubulin
Immunogen
A peptide corresponding to detyrosinated α-tubulin
Clone Designation
RM444
100 µl of protein A-affinity purified monoclonal antibody.
Storage Buffer
PBS with 50% glycerol, 1% BSA, and 0.09% sodium azide
Host
Rabbit
Isotype
IgG
Applications
ICC, IF, WB
Cross Reactivity
(+) Detyrosinated α-tubulin
Species Reactivity
(+) Human
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Detyrosinated α-tubulin is a form of the cytoskeletal protein α-tubulin that has been post-translationally modified by the tubulin carboxypeptidases vasohibin 1 (VASH-1) and VASH-2, which remove the C-terminal tyrosine from α-tubulin.1 Detyrosination of α-tubulin occurs in the cytosol and exposes two consecutive glutamate residues that can be further processed to form Δ2- or Δ3-tubulin. Detyrosinated α-tubulin monomers can be re-tyrosinated by tubulin tyrosine ligase and be incorporated into microtubules again. α-Tubulin detyrosination is associated with, but not sufficient for, increased stability of the microtubule and is involved in a variety of biological processes, including neuronal development, β-oxidation, mitosis, and cardiomyocyte contraction.2,3,1,4 Increased levels of detyrosination are associated with tumor development in vitro, have been found in tumor tissue from patients with breast cancer, and are positively correlated with breast cancer aggressiveness.5,6 Cayman’s Detyrosinated α-Tubulin Rabbit Monoclonal Antibody (Clone RM444) can be used for immunocytochemistry (ICC), immunofluorescence (IF), and Western blot (WB) applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Nieuwenhuis, J., and Brummelkamp, T.R. The tubulin detyrosination cycle: Function and enzymes. Trends Cell Biol. 29(1), 80-92 (2019).

    2. Chen, J., Kholina, E., Szyk, A., et alα-tubulin tail modifications regulate microtubule stability through selective effector recruitment, not changes in intrinsic polymer dynamics. Dev. Cell 56(14), 2016-2028.e2014 (2021).

    3. Herms, A., Bosch, M., Reddy, B.J.N., et alAMPK activation promotes lipid droplet dispersion on detyrosinated microtubules to increase mitochondrial fatty acid oxidation. Nat. Commun. 6, 7176 (2015).

    4. Chen, C.Y., Caporizzo, M.A., Bedi, K., et alSuppression of detyrosinated microtubules improves cardiomyocyte function in human heart failure. Nat. Med. 24(8), 1225-1233 (2018).

    5. Wattanathamsan, O., and Pongrakhananon, V. Post-translational modifications of tubulin: Their role in cancers and the regulation of signaling molecules. Cancer Gene Ther. (2021).

    6. Mialhe, A., Lafanechère, L., Peloux, I.T.N., et alTubulin detyrosination is a frequent occurrence in breast cancers of poor prognosis. Cancer Res. 61(13), 5024-5027 (2001).