mProX™ Human HIPK2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 MBR in HIPK2-depleted cells.
HeLa cells were transfected with siRNA specific to HIPK2 or a negative universal control. Four and five days after transfection, the cells were examined by WB using the specified Abs to confirm RNAi and by IF for MBR quantification using β-tubulin staining in conjunction with CEP55 as the MBR marker.
Ref: Sardina, Francesca, et al. "HIPK2 is required for midbody remnant removal through autophagy-mediated degradation." Frontiers in Cell and Developmental Biology 8 (2020): 572094.
Pubmed: 33043004
DOI: 10.3389/fcell.2020.572094
Research Highlights
The notion that HIPK2 is a major participant in many cancer forms is supported by all of these results, and as such, it may serve as a significant prognostic marker, a predictor of therapy response, or even a therapeutic target in and of itself.
Conte, Andrea, et al. "HIPK2 in cancer biology and therapy: Recent findings and future perspectives." Cellular Signalling 101 (2023): 110491.
Pubmed:
36241057
DOI:
10.1016/j.cellsig.2022.110491
By lowering P-P53, exercise-induced HIPK2 suppression prevents MI and lessens the death of cardiomyocytes. One potential innovative treatment strategy for MI is the inhibition of HIPK2.
Zhou, Qiulian, et al. "Exercise downregulates HIPK2 and HIPK2 inhibition protects against myocardial infarction." EBioMedicine 74 (2021).
Pubmed:
34837851
DOI:
10.1016/j.ebiom.2021.103713