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TP53BP2 encodes a member of the ASPP (apoptosis-stimulating protein of p53) family of p53 interacting proteins. Zusätzlich bieten wir Ihnen Tumor Protein P53 Binding Protein 2 Antikörper (71) und Tumor Protein P53 Binding Protein 2 Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.
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These findings uncover a novel role of Aspp2 in regulating vertebrate embryonic growth.
These findings identify TP53BP2 as a strong candidate causative gene for central nervous system (CNS) defects in 1q41q42 microdeletion syndrome.
SPP2 dominates the biological outcome, thus switching from a Gal-1 supported growth-promoting setting to a senescence inducing and stemness suppressive program in cancer cells. Our results support Ras nanocluster as major integrators of tumour fate decision events.
After genotoxic stress, Aspp1 (zeige PPP1R13B ELISA Kits) promotes hematopoietic stem cell (HSC (zeige FUT1 ELISA Kits)) cycling and induces p53 (zeige TP53 ELISA Kits)-dependent apoptosis in cells with persistent DNA damage foci. Aspp1 (zeige PPP1R13B ELISA Kits) also attenuates HSC (zeige FUT1 ELISA Kits) self-renewal and accumulation of DNA damage in p53 (zeige TP53 ELISA Kits) null HSCs.
ASPP2 may participate in the lipid metabolism of non-alcoholic steatohepatitis and attenuate liver failure.
ASPP2 prevents beta-catenin (zeige CTNNB1 ELISA Kits) from transactivating ZEB1 (zeige ZEB1 ELISA Kits) directly by forming an ASPP2-beta-catenin (zeige CTNNB1 ELISA Kits)-E-cadherin (zeige CDH1 ELISA Kits) ternary complex
findings suggest that the identified STAT1 (zeige STAT1 ELISA Kits)/ASPP2 pathway may connect tumor suppression and cell polarity to neuroinflammation
our studies demonstrate the role of Siah2 (zeige SIAH2 ELISA Kits) in regulation of tight junction integrity and cell polarity under hypoxia, through its regulation of ASPP2 stability.
ASPP2 is a tumor suppressor that suppresses squamous cell carcinoma via inflammatory signaling through NF-kappaB (zeige NFKB1 ELISA Kits)-mediated repression of p63 (zeige CKAP4 ELISA Kits).
Our study demonstrates a novel role for ASPP1 (zeige PPP1R13B ELISA Kits) and ASPP2 in the death of retinal ganglion cells.
regulates epithelial cell polarity in cooperation with PAR-3 (zeige F2RL2 ELISA Kits) to form an active PAR (zeige AFG3L2 ELISA Kits) complex
Results showed that protein expression levels of ASPP2 and P53 (zeige TP53 ELISA Kits) were significantly higher in esophageal squamous cell carcinoma tissues than in paired noncancerous tissues.
Expression levels of TP53BP2, FBXO28 (zeige FBXO28 ELISA Kits), and FAM53A genes were associated with patient survival specifically in ER-positive, TP53 (zeige TP53 ELISA Kits)-mutated tumors.
These data together implicated a critical impact of MiR (zeige MLXIP ELISA Kits)-205/ASPP2 on promoting epithelial-mesenchymal transition.
ASPP2 is a key regulator of BECN1 (zeige BECN1 ELISA Kits)-dependent autophagy.
ASPP2 suppresses invasion, peritoneal dissemination and TGF-beta1 (zeige TGFB1 ELISA Kits)-induced EMT (zeige ITK ELISA Kits) by inhibiting Smad7 (zeige SMAD7 ELISA Kits) degradation mediated by ITCH in gastric cancer cells.
Our results suggest that Gal-1 and ASPP2 functionally compete in nanocluster for active Ras on the plasma membrane. ASPP2 dominates the biological outcome, thus switching from a Gal-1 supported growth-promoting setting to a senescence inducing and stemness suppressive program in cancer cells. Our results support Ras nanocluster as major integrators of tumour fate decision events.
ASPP2 suppresses p53 (zeige TP53 ELISA Kits) target gene transactivation, promoter occupancy, and endogenous p53 (zeige TP53 ELISA Kits) target gene expression in response to DNA damage
In this study, in recombinant adenovirus-ASPP2-infected HepG2 cells, ASPP2 overexpression induces amphiregulin (zeige AREG ELISA Kits) expression in a p53 (zeige TP53 ELISA Kits)-dependent manner
Downregulated expression of ASPP2 is associated with hepatocellular carcinoma.
This gene encodes a member of the ASPP (apoptosis-stimulating protein of p53) family of p53 interacting proteins. The protein contains four ankyrin repeats and an SH3 domain involved in protein-protein interactions. It is localized to the perinuclear region of the cytoplasm, and regulates apoptosis and cell growth through interactions with other regulatory molecules including members of the p53 family. Multiple transcript variants encoding different isoforms have been found for this gene.
tumor protein p53 binding protein, 2
, apoptosis-stimulating of p53 protein 2-like
, apoptosis-stimulating of p53 protein 1
, protein phosphatase 1 regulatory subunit 13B
, transformation related protein 53 binding protein 2
, tumor protein p53-binding protein, 2
, apoptosis-stimulating of p53 protein 2
, p53-binding protein 2
, tumor suppressor p53-binding protein 2
, BCL2-binding protein
, apoptosis-stimulating protein of p53, 2
, renal carcinoma antigen NY-REN-51