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displays increased expression in response to stress. Additionally we are shipping Tumor Protein P53 Inducible Nuclear Protein 1 Proteins (3) and and many more products for this protein.
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Human Polyclonal TP53INP1 Primary Antibody for IHC, WB - ABIN223065
Erster, Mihara, Kim, Petrenko, Moll: In vivo mitochondrial p53 translocation triggers a rapid first wave of cell death in response to DNA damage that can precede p53 target gene activation. in Molecular and cellular biology 2004
Knockout of miR (show MLXIP Antibodies)-155 in cardiac fibroblasts improves cardiac remodeling by targeting TP53INP1.
These data provide evidence that the TP53INP1 gene prevents metabolic syndrome, through a mechanism involving prevention of oxidative stress by mitochondrial homeostasis regulation.
Nanog enhances miR-17/92 cluster expression that in turn targets Trp53inp1, thus contributing to release neural stem cell self-renewal constraints.
TP53INP1 loss of expression contributes to pancreatic cancer formation in a conditional KrasG12D mouse model.
these data emphasize the role of TP53INP1 in protection against cell injury
Data show that induction of the stress-induced proteins (SIPs) SIP18 and SIP27, in human- and mouse-derived cell lines, is absent from cells with deleted, mutated or inactive p53 (show TP53 Antibodies), suggesting that regulation of SIP (show CACYBP Antibodies) gene expression is dependent on p53 (show TP53 Antibodies).
TP53INP1s are functionally associated with p73 (show ARHGAP24 Antibodies) to regulate cell cycle progression and apoptosis.
Tumor protein 53 (show TP53 show)-induced nuclear protein 1 (show NUPR1 show) is a potential target for the prevention of colorectal cancer in patients with inflammatory bowel disease[Tumor protein 53 (show TP53 show)-induced nuclear protein 1 (show NUPR1 show)]
Study elucidated StarD13 (show STARD13 Antibodies) messenger RNA as a Competitive endogenous messenger RNA (ceRNA) in regulating migration and invasion of breast cancer cells. MicroRNA-125b was identified to induce metastasis of MCF-7 cells and bind with both StarD13 (show STARD13 Antibodies) 3'UTR (show UTS2R Antibodies) and TP53INP1 3'UTR (show UTS2R Antibodies). Therefore, a ceRNA interaction between StarD13 (show STARD13 Antibodies) and TP53INP1 mediated by competitively binding to miR (show MLXIP Antibodies)-125b was indicated.
Upregulated miR (show MLXIP Antibodies)-200a enhances treatment resistance via antagonizing TP53INP1 and YAP1 (show YAP1 Antibodies) in breast cancer.
these results revealed that TP53INP1 is a target gene of miR (show MLXIP Antibodies)-504 and that miR (show MLXIP Antibodies)-504 enhances osteosarcoma growth and promotes distant metastases by targeting TP53INP1. Thus, miR (show MLXIP Antibodies)-504/TP53INP1 may be associated with osteosarcoma size and clinical stage.
Low TP53INP1 expression is associated with Metastasis of Hepatocellular Carcinoma.
Negative TP53INP1 protein levels correlated with a poor outcome in pediatric ependymoma. Direct binding of miR (show MLXIP Antibodies)-124-3p to its target TP53INP1 is demonstrated.
Results showed that TP53INP1 and E-cadherin (show CDH1 Antibodies) mRNA and protein were significantly down-regulated in glioma tumors and positively correlated with higher grade and poor survival. Also, the study provides evidence that TP53INP1 3'-UTR (show UTS2R Antibodies) could inhibit the epithelial-mesenchymal transition, thus hindering the migration and invasion of glioma via acting as a competitive endogenous RNA for E-cadherin (show CDH1 Antibodies).
miR (show MLXIP Antibodies)-205/TP53INP1 mediated autophagy pathway might be an important molecular mechanism regulating radiosensitivity of prostate cancer cells
silencing of TP53inp1 leads radiation induced autophagy impairment and induces accumulation of damaged mitochondria in primary human fibroblasts.
MicroRNA205 promotes the tumorigenesis of nasopharyngeal carcinoma through targeting TP53INP1 protein.
FOXP1 (show FOXP1 Antibodies), TP53INP1, TNFAIP3 (show TNFAIP3 Antibodies), and TUSC2 (show TUSC2 Antibodies) were identified as miR (show MLXIP Antibodies)-19a targets.
displays increased expression in response to stress
tumor protein p53-inducible nuclear protein 1
, tumor protein p53 inducible nuclear protein 1
, p53-dependent damage-inducible nuclear protein 1
, stress induced protein
, stress-induced protein
, thymus expressed acidic protein
, thymus-expressed acidic protein
, p53-inducible p53DINP1
, transformation related protein 53 inducible nuclear protein 1