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SPOP encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. Additionally we are shipping Speckle-Type POZ Protein Antibodies (56) and Speckle-Type POZ Protein Kits (20) and many more products for this protein.
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Human SPOP Protein expressed in Escherichia coli (E. coli) - ABIN667901
Furukawa, He, Borchers, Xiong: Targeting of protein ubiquitination by BTB-Cullin 3-Roc1 ubiquitin ligases. in Nature cell biology 2003
Show all 2 references for ABIN667901
Dzip1 (show DZIP1 Proteins)-dependent stabilization of Spop/HIB is evolutionarily conserved and essential for proper regulation of Gli (show GLI1 Proteins)/Ci proteins in the Hh pathway.
Data indicate that a mutation in the SPOP gene may not be associated with breast cancer, particularly in Chinese women.
SPOP acts as a tumor suppressor by promoting senescence through degrading SENP7 (show SENP7 Proteins).
our findings emphasize the critical role of SPOP in the regulation of proliferation and migration in liver cancer
results suggest that SPOP plays a pivotal role in colorectal cancer (CRC (show CALR Proteins)) through mesenchymal-epithelial transition and matrix metalloproteases.
SPOP functions as a tumor suppressor to negatively regulate the stability of the ERG (show ERG Proteins) oncoprotein in prostate cancer.
Overcoming ERG (show ERG Proteins) resistance to SPOP-mediated degradation represents a viable strategy for treatment of prostate cancers expressing either mutated SPOP or truncated ERG (show ERG Proteins).
Our study revealed novel molecular mechanisms underlying the regulation of ERa protein and provided insights in understanding the relationship between SPOP mutations and the development of endometrial cancer.
SPOP plays critical roles in suppressing gastric tumorigenesis through inhibiting Hh/Gli2 signaling pathway. It may provide an alternative strategy for developing therapeutic agents of gastric cancer in future.
SPOP mutations and novel variants were detected in 5 of 27 aggressive PCa (show FLVCR1 Proteins) and one of 22 less aggressive PCa (show FLVCR1 Proteins)
SPOP has potential use as novel biomarker of glioma and may serve as an independent predictive factor for prognosis of glioma patients.
These results implicate SPOP as a novel participant in DNA double strand break repair and suggest that SPOP mutation drives prostate tumorigenesis in part through genomic instability.
miR (show MLXIP Proteins)-145 has a role in post-transcriptional regulation of SPOP expression in selected tissues.
similar S/T-rich motifs are present in Gli (show GLI1 Proteins) proteins as well as in numerous HIB-interacting proteins and mediate Gli (show GLI1 Proteins) degradation by SPOP
MacroH2A1.2 (show H2AFY Proteins) binds the nuclear protein Spop.
Interaction of endogenous PDX-1 (show PDX1 Proteins) and PCIF1 in MIN6 insulinoma (show RPS15 Proteins) cells, is demonstarted.
This gene encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. In mouse, the encoded protein binds to the putative leucine zipper domain of macroH2A1.2, a variant H2A histone that is enriched on inactivated X chromosomes. The BTB/POZ domain of this protein has been shown in other proteins to mediate transcriptional repression and to interact with components of histone deacetylase co-repressor complexes. Alternative splicing of this gene results in multiple transcript variants encoding the same protein.
speckle-type POZ protein
, Speckle-type POZ protein
, speckle-type POZ protein-like
, HIB homolog 1
, speckle-type POZ protein B
, roadkill homolog 1
, PDX-1 C-terminal-interacting factor 1