Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
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. Zusätzlich bieten wir Ihnen Speckle-Type POZ Protein Antikörper (58) und Speckle-Type POZ Protein Proteine (11) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 20 products:
Dzip1-dependent stabilization of Spop/HIB is evolutionarily conserved and essential for proper regulation of Gli (zeige GLI1 ELISA Kits)/Ci proteins in the Hh pathway.
methylation status of SPOP promoter can be used as a novel epigenetic biomarker and a therapeutic target in colorectal cancer.
these data highlight SPOP as an important regulator of luminal epithelial cell proliferation and c-MYC (zeige MYC ELISA Kits) expression in prostate physiology, identify c-MYC (zeige MYC ELISA Kits) as a novel bona fide SPOP substrate, and help explain the frequent inactivation of SPOP in human prostate adenocarcinoma.
Results elucidate the tumor-suppressor role of SPOP in prostate cancer in which it acts as a negative regulator of BET protein stability and also provide a molecular mechanism for resistance to BET inhibitors in individuals with prostate cancer bearing SPOP mutations.
SPOP mutation in endometrial cancer increased degradation of BRD2 (zeige BRD2 ELISA Kits), BRD3 (zeige BRD3 ELISA Kits) and BRD4 (zeige BRD4 ELISA Kits) proteins. SPOP mutation in prostate cancer increased expression of BRD2 (zeige BRD2 ELISA Kits), BRD3 (zeige BRD3 ELISA Kits) and BRD4 (zeige BRD4 ELISA Kits) proteins.
Prostate cancer-derived SPOP mutants failed to interact with Cdc20 (zeige CDC20 ELISA Kits) to promote its degradation. As a result, SPOP-deficient prostate cancer cells with elevated Cdc20 (zeige CDC20 ELISA Kits) expression became resistant to a pharmacological Cdc20 (zeige CDC20 ELISA Kits) inhibitor.
While wild-type SPOP localizes to liquid nuclear speckles, self-association-deficient SPOP mutants have a diffuse distribution in the nucleus. SPOP oligomerizes through its BTB and BACK domains.
SPOP mutation activates both PI3K (zeige PIK3CA ELISA Kits)/mTOR (zeige FRAP1 ELISA Kits) and androgen receptor (zeige AR ELISA Kits) signaling, effectively uncoupling the normal negative feedback between these two pathways.
SPOP-containing complex regulates SETD2 stability and H3K36me3-coupled alternative splicing.
The levels of SPOP significantly decreased, while the levels of SIRT2 (zeige SIRT2 ELISA Kits) significantly increased in non-small cell lung cancer (NSCLC) cell lines, compared to normal bronchial epithelial cell line and NSCLC specimens, compared to the paired non-tumor lung tissue.
hese findings reveal novel molecular events underlying the regulation of INF2 (zeige INF2 ELISA Kits) function and localization, and provided insights in understanding the relationship between SPOP mutations and dysregulation of mitochondrial dynamics in prostate cancer.
loss of Spop, but not Spopl, disrupts chondrocyte hypertrophy and osteoblast differentiation in the mouse, suggesting the requirement for Spop-mediated protein degradation in mouse skeletal development; overexpressed Spop targets both Gli3FL (zeige GLI3 ELISA Kits) and Gli3R for ubiquitination and degradation and Spop is an important positive regulator of Ihh (zeige IHH ELISA Kits) signaling and skeletal development
Results demonstrate a negative role of Spop in the level and activity of Gli3 (zeige GLI3 ELISA Kits), Shh (zeige SHH ELISA Kits) signaling and ventral spinal cord patterning.
Speckle-type pox virus and zinc finger (POZ) protein (SPOP) regulates endometrial stromal cell decidualization in mice and that hormones regulate the expression of SPOP. This study suggests that ubiquitination may be involved in embryonic implantation.
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 (zeige MLXIP ELISA Kits)-145 has a role in post-transcriptional regulation of SPOP expression in selected tissues.
similar S/T-rich motifs are present in Gli (zeige GLI1 ELISA Kits) proteins as well as in numerous HIB-interacting proteins and mediate Gli (zeige GLI1 ELISA Kits) degradation by SPOP
MacroH2A1.2 binds the nuclear protein (zeige HEMGN ELISA Kits) Spop.
Interaction of endogenous PDX-1 (zeige PDX1 ELISA Kits) and PCIF1 in MIN6 insulinoma (zeige RPS15 ELISA Kits) 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