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CIAPIN1 is a cytokine-induced inhibitor of apoptosis with no relation to apoptosis regulatory molecules of the BCL2 (MIM 151430) or CASP (see MIM 147678) families. Zusätzlich bieten wir Ihnen Cytokine Induced Apoptosis Inhibitor 1 Antikörper (72) und Cytokine Induced Apoptosis Inhibitor 1 Proteine (12) und viele weitere Produktgruppen zu diesem Protein an.
results of the present study suggest that downregulation of the CIAPIN1 gene in multiple myeloma cells may be associated with the development of this disease.
CIAPIN1 and ABCA13 may be novel markers of poor outcome in pre-chemotherapy serous carcinoma effusions.
CIAPIN1 over-expression decreases NHE1 (zeige SLC9A1 ELISA Kits) expression and ERK1/2 (zeige MAPK1/3 ELISA Kits) phosphorylation.
lentivirus-vector-mediated RNAi targeting of CIAPIN1 is a potential approach to reverse MDR of breast cancer and CIAPIN1 may participate in MDR of breast cancer by regulating P-glycoprotein and P53 (zeige TP53 ELISA Kits) expression.
the 25-kDa cleaved fragment of anamorsin was detected in post-mortem brains of Alzheimer and Parkinson (zeige CASP3 ELISA Kits) disease patients
The N-terminal methyltransferase-like domain of anamorsin probably functions as a structural scaffold to inhibit methyl transfers.
CIAPIN1 targeted NHE1 (zeige SLC9A1 ELISA Kits) to mediate differentiation of K562 cells via ERK1/2 (zeige MAPK1/3 ELISA Kits) pathway.
Mossbauer and EPR (zeige EREG ELISA Kits) spectra of human anamorsin show that both the M1 motif and the M2 motif bind independently a [2Fe-2S] cluster through the four cysteines of each motif.
CIAPIN1 siRNA inhibited proliferation, migration and promotes apoptosis of vascular smooth muscle cells by regulating Bcl-2 (zeige BCL2 ELISA Kits) and Bax (zeige BAX ELISA Kits).
the molecular basis of recognition between Ndor1 (zeige NDOR1 ELISA Kits) and anamorsin and of the electron transfer process, was investigated.
Among 46 putative substrates identified in MN9D neuronal cells, we further evaluated whether caspase-3 (zeige CASP3 ELISA Kits)-mediated cleavage of anamorsin, a recently recognized cell death-defying factor in hematopoiesis, is a general feature of apoptosis.
These data suggest that PKCtheta;, PKCdelta, and p38MAPK activation lead to cell cycle retardation in AM KO MEF cells, and that AM may negatively regulate novel PKCs and p38MAPK in MEF cells.
Anamorsin is considered to be a necessary molecule for hematopoiesis that mediates antiapoptotic effects of various cytokines.
CIAPIN1 was localized in both the cytoplasm and the nucleus and was accumulated in the nucleolus. Bioinformatic prediction disclosed a putative nuclear localization signal and a putative nuclear export signal within mouse CIAPIN1.
CIAPIN1 is a cytokine-induced inhibitor of apoptosis with no relation to apoptosis regulatory molecules of the BCL2 (MIM 151430) or CASP (see MIM 147678) families. Expression of CIAPIN1 is dependent on growth factor stimulation (Shibayama et al., 2004
, cytokine-induced apoptosis inhibitor 1
, fe-S cluster assembly protein DRE2 homolog
, cytokine induced apoptosis inhibitor 1
, Fe-S cluster assembly protein DRE2 homolog
, Cytokine-induced apoptosis inhibitor 1
, predicted protein of HQ0915