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PDP - Template Name: Antibody Sampler Kit
PDP - Template ID: *******4a3ef3a
  1. Products /
  2. Primary Antibodies /
  3. Mouse Reactive DNA Demethylation Antibody Sampler Kit

Mouse Reactive DNA Demethylation Antibody Sampler Kit #19206

    Product Information

    Kit Usage Information

    Protocols

    Product Description

    The Mouse Reactive DNA Demethylation Antibody Sampler Kit provides an economical means of detecting TET protein family members and TDG protein. The kit includes enough antibodies to perform two western blot experiments with each primary antibody.

    Specificity / Sensitivity

    Each antibody in the Mouse Reactive DNA Demethylation Antibody Sampler Kit detects endogenous levels of its target protein. TDG (E5T5G) Rabbit mAb recognizes endogenous levels of total and SUMOylated TDG protein and may detect a band of unknown origin at 200 kDa in some rodent and monkey cell lines.

    Source / Purification

    Monoclonal antibodies are produced by immunizing animals with synthetic peptides corresponding to residues near the carboxy terminus of mouse TET1 protein, Val1640 of mouse TET2 protein, and recombinant proteins specific to the carboxy termini of human TET3 and TDG proteins.

    Background

    Methylation of DNA at cytosine residues is a heritable, epigenetic modification that is critical for proper regulation of gene expression, genomic imprinting, and mammalian development (1,2). 5-methylcytosine is a repressive epigenetic mark established de novo by two enzymes, DNMT3a and DNMT3b, and is maintained by DNMT1 (3,4). 5-methylcytosine was originally thought to be passively depleted during DNA replication. However, subsequent studies have shown that Ten-Eleven Translocation (TET) proteins TET1, TET2, and TET3 can catalyze the oxidation of methylated cytosine to 5-hydroxymethylcytosine (5-hmC) (5). Additionally, TET proteins can further oxidize 5-hmC to form 5-formylcytosine (5-fC) and 5-carboxylcytosine (5-caC), both of which are excised by thymine-DNA glycosylase (TDG), effectively linking cytosine oxidation to the base excision repair pathway and supporting active cytosine demethylation (6,7). TET1 is highly expressed in embryonic stem cells and is essential for maintaining stem cell pluripotency (8). Aberrant TET1 expression has also been implicated in a variety of cancers, including hepatocellular carcinoma, T-cell acute lymphoblastic leukemia (T-ALL), and triple-negative breast cancer (TNBC), among others (9-11). TET2 is frequently mutated in myeloid dysplastic syndrome (MDS) and diffuse large B-cell lymphomas (12,13). TET2 protein expression is often reduced in solid tumors such as prostate cancer, melanoma, and oral squamous cell carcinoma (14-16). TET3 plays key roles in regulating early development and neonatal growth (17,18). TET2/TET3 deficiency can lead to myeloid cell, B cell, and invariant natural killer T (iNKT) cell malignancies. In Tregs, TET2/TET3 deficiency in mice leads to hyperproliferation and inflammatory disease (19,20). Knockout or catalytic inactivation of TDG leads to embryonic lethality (21,22). SUMOylation of TDG has been reported to help it dissociate from its abasic product, thereby increasing catalytic turnover (23). Additional studies suggest that SUMOylation affects TDG’s cellular localization or lowers its base excision activity, allowing it to act as a ‘reader’ protein for 5-fC and 5-caC modified DNA (24).
    1. Hermann, A. et al. (2004) Cell Mol Life Sci 61, 2571-87.
    2. Turek-Plewa, J. and Jagodziński, P.P. (2005) Cell Mol Biol Lett 10, 631-47.
    3. Okano, M. et al. (1999) Cell 99, 247-57.
    4. Li, E. et al. (1992) Cell 69, 915-26.
    5. Tahiliani, M. et al. (2009) Science 324, 930-5.
    6. He, Y.F. et al. (2011) Science 333, 1303-7.
    7. Ito, S. et al. (2011) Science 333, 1300-3.
    8. Ito, S. et al. (2010) Nature 466, 1129-33.
    9. Shirai, K. et al. (2021) Cancer Sci 112, 2855-2869.
    10. Bamezai, S. et al. (2021) Leukemia 35, 389-403.
    11. Good, C.R. et al. (2018) Cancer Res 78, 4126-4137.
    12. Langemeijer, S.M. et al. (2009) Nat Genet 41, 838-42.
    13. Asmar, F. et al. (2013) Haematologica 98, 1912-20.
    14. Nickerson, M.L. et al. (2013) Hum Mutat 34, 1231-41.
    15. Lian, C.G. et al. (2012) Cell 150, 1135-46.
    16. Jäwert, F. et al. (2013) Anticancer Res 33, 4325-8.
    17. Peat, J.R. et al. (2014) Cell Rep 9, 1990-2000.
    18. Tsukada, Y. et al. (2015) Sci Rep 5, 15876.
    19. Nakatsukasa, H. et al. (2019) Int Immunol 31, 335-347.
    20. Yue, X. et al. (2019) Nat Commun 10, 2011.
    21. Cortellino, S. et al. (2011) Cell 146, 67-79.
    22. Cortázar, D. et al. (2011) Nature 470, 419-23.
    23. Hardeland, U. et al. (2002) EMBO J 21, 1456-64.
    24. Coey, C.T. and Drohat, A.C. (2018) Nucleic Acids Res 46, 5159-5170.

    Database Links

    UniProt ID: O43151 , Q4JK59 , Q3URK3 , Q13569


    Entrez-Gene Id: 200424 , 214133 , 52463 , 6996


    Limited Uses

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    For Research Use Only. Not For Use In Diagnostic Procedures.
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