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Ornithine decarboxylase (ODC) catalyzes the conversion of ornithine to putrescine in the first and apparently rate-limiting step in polyamine biosynthesis.
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e in vivo experiment confirmed that this RNA editing confers higher capacity of tumor migration as well. In conclusion, antizyme inhibitor 1 RNA editing and its involvement in tumorigenesis of non-small-cell lung cancer pave a new way for potential clinical management of non-small-cell lung cancer.
AzI1 fulfils an essential regulatory function in polyamine homeostasis and cell proliferation.
Data show the the interplay between the enzyme ornithine decarboxylase (ODC) and two regulatory proteins: antizyme (Az) and inhibitor (AzIN).
This study also suggests that highly expressed AZI (Montrer OAZ1 Kits ELISA) may be partly responsible for increased ODC (Montrer ODC1 Kits ELISA) activity and cellular transformation.
AZIN1 rs2679757 and TRPM5 rs886277 are associated with the risk of HBV-related liver cirrhosis in Chinese.
edited form has a stronger affinity to antizyme, and the resultant higher AZIN1 protein stability promotes cell proliferation through the neutralization of antizyme-mediated degradation of ornithine decarboxylase (ODC (Montrer ODC1 Kits ELISA)) and cyclin D1 (Montrer CCND1 Kits ELISA)
minor allelic SNP variant in 12th exon of AZIN1 associated with slower rates of fibrosis progression favors expression of novel splice form, AZIN1 SV2, that inhibits expression of fibrogenic genes in hepatic stellate cells.
AZ_95-176 is the minimal AZ peptide that is fully functioning in the binding of ODC (Montrer ODC1 Kits ELISA) and AZI (Montrer OAZ1 Kits ELISA) and inhibition of their function.
SNP rs2679757 in the AZIN1 gene is associated with the risk of HBV-related liver cirrhosis in Chinese patients.
Decreased ornithine decarboxylase (Montrer ODC1 Kits ELISA) is associated with prostate cancer.
The polyamines regulate two novel steps of Azin1 expression, namely the transcription and a particular splicing pattern, both of which may affect the level of mRNA encoding the full-length active Azin1 protein.
miR (Montrer MLXIP Kits ELISA)-433 is an important component of TGF-beta (Montrer TGFB1 Kits ELISA)/Smad3 (Montrer SMAD3 Kits ELISA)-induced renal fibrosis through the induction of a positive feedback loop to amplify TGF-beta (Montrer TGFB1 Kits ELISA)/Smad3 (Montrer SMAD3 Kits ELISA) signaling.
AZI plays an important role in regulating the levels of Ornithine decarboxylase (Montrer ODC1 Kits ELISA), putrescine and spermidine in mice, and is essential for the survival of mice.
differences in the subcellular distribution of AZIN1 and AZIN2 (Montrer ADC Kits ELISA)
The data-driven docking results suggest that both proteins occupy the same binding site on Az1, with Az1 binding within a large groove in antizyme (Montrer OAZ1 Kits ELISA) inhibitor (AzI) and
Ornithine decarboxylase (ODC) catalyzes the conversion of ornithine to putrescine in the first and apparently rate-limiting step in polyamine biosynthesis. Ornithine decarboxylase antizymes play a role in the regulation of polyamine synthesis by binding to and inhibiting ornithine decarboxylase. The protein encoded by this gene is highly similar to ODC. It binds to ODC antizyme and stabilizes ODC, thus inhibiting antizyme-mediated ODC degradation. Two alternatively spliced transcript variants have been found for this gene.
, ornithine decarboxylase antizyme inhibitor
, ODC antizyme inhibitor
, antizyme inhibitor 1
, Antizyme inhibitor 1
, ODC antizyme
, ornithine decarboxylase antizyme 1