Human Recombinant SUV420H2 protein, GST Tag (V2LY-0526-LY7022)

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Basic Information

Expressed Host
E. coli
Protein Species
Human
Tag
GST Tag
Protein Construction
This product is Human Recombinant SUV420H2 protein, GST Tag consist of Amino Acid: 2-280 and predicts a molecular mass of 60 kDa.
Molecule Mass
60 kDa
Sequence
Amino Acid: 2-280
Species
Human

Formulations & Storage [For reference only, actual COA shall prevail!]

Purity
>80% as determined by SDS-PAGE
Endotoxin
Please contact us for more information.
Format
Liquid
Buffer
Tris, NaCl
Preservative
None
Storage
Samples are stable for up to twelve months from date of receipt at -20°C to -80°C. Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
More Infomation

Target

Full Name
Lysine Methyltransferase 5C
Function
Histone methyltransferase that specifically methylates monomethylated 'Lys-20' (H4K20me1) and dimethylated 'Lys-20' (H4K20me2) of histone H4 to produce respectively dimethylated 'Lys-20' (H4K20me2) and trimethylated 'Lys-20' (H4K20me3) and thus regulates transcription and maintenance of genome integrity (PubMed:24396869, PubMed:28114273).
In vitro also methylates unmodified 'Lys-20' (H4K20me0) of histone H4 and nucleosomes (PubMed:24396869).
H4 'Lys-20' trimethylation represents a specific tag for epigenetic transcriptional repression. Mainly functions in pericentric heterochromatin regions, thereby playing a central role in the establishment of constitutive heterochromatin in these regions. KMT5C is targeted to histone H3 via its interaction with RB1 family proteins (RB1, RBL1 and RBL2) (By similarity).
Facilitates TP53BP1 foci formation upon DNA damage and proficient non-homologous end-joining (NHEJ)-directed DNA repair by catalyzing the di- and trimethylation of 'Lys-20' of histone H4 (PubMed:28114273).
May play a role in class switch reconbination by catalyzing the di- and trimethylation of 'Lys-20' of histone H4 (By similarity).
Biological Process
Chromatin organizationIEA:UniProtKB-KW
DNA repairManual Assertion Based On ExperimentIMP:UniProtKB
Histone H4-K20 dimethylationIEA:InterPro
Histone H4-K20 trimethylationManual Assertion Based On ExperimentIBA:GO_Central
Positive regulation of double-strand break repair via nonhomologous end joiningManual Assertion Based On ExperimentIMP:UniProtKB
Positive regulation of isotype switchingISS:UniProtKB
Cellular Location
Nucleus
Chromosome
Associated with pericentric heterochromatin. CBX1 and CBX5 are required for the localization to pericentric heterochromatin (By similarity).

Montealegre, A. A. (2023). The role of KMT5C on EGFR inhibitor resistance in non-small cell lung cancer (Doctoral dissertation, Purdue University Graduate School).

Tong, Y., Wang, F., Li, S., Guo, W., Li, Q., Qian, Y., ... & Liu, Y. (2023). Histone methyltransferase KMT5C drives liver cancer progression and directs therapeutic response to PARP inhibitors. Hepatology, 10-1097.

Agredo, A., Pal, A., Son, J., Lanman, N. A., & Kasinski, A. L. (2023). Loss of the methyltransferase KMT5C drives resistance to tyrosine kinase inhibitors via H4K20me3 regulation in non-small cell lung cancer. Cancer Research, 83(7_Supplement), 4752-4752.

Pal, A. S., Agredo, A., Lanman, N. A., Son, J., Sohal, I. S., Bains, M., ... & Kasinski, A. L. (2022). Loss of KMT5C promotes EGFR inhibitor resistance in NSCLC via LINC01510-mediated upregulation of MET. Cancer Research, 82(8), 1534-1547.

Strickfaden, H., Missiaen, K., Knechtel, J. W., Hendzel, M. J., & Underhill, D. A. (2021). KMT5C encodes robust heterochromatin retention and liquid-like behavior using limited sequence features. bioRxiv, 2021-11.

Zhao, Q., Zhang, Z., Rong, W., Jin, W., Yan, L., Jin, W., ... & Pan, D. (2020). KMT5c modulates adipocyte thermogenesis by regulating Trp53 expression. Proceedings of the National Academy of Sciences, 117(36), 22413-22422.

Gao, J., Li, E., Liu, W., Yang, Q., Xie, C., Ai, J., ... & Wu, L. (2020). Circular RNA MYLK promotes hepatocellular carcinoma progression through the miR29a/KMT5C signaling pathway. OncoTargets and therapy, 8615-8627.

Strickfaden, H., Missiaen, K., Hendzel, M. J., & Underhill, D. A. (2019). KMT5C displays robust retention and liquid-like behavior in phase separated heterochromatin. BioRxiv, 776625.

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For research use only. Not intended for any clinical use.

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