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PPP1R8, through alternative splicing, encodes three different isoforms. De plus, nous expédions Protein Phosphatase 1, Regulatory Subunit 8 Anticorps (98) et Protein Phosphatase 1, Regulatory Subunit 8 Protéines (9) et beaucoup plus de produits pour cette protéine.
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NIPP1 could be activated by hypoxia and contributed to hypoxia-induced invasive and metastatic potential in hepatocellular carcinoma.
The results observed an inverse correlation between the expression of NAA10 (Montrer ARD1A Kits ELISA) and that of miR (Montrer MLXIP Kits ELISA)-342-5p and miR (Montrer MLXIP Kits ELISA)-608 .
Human Naa15 (NATH (Montrer NAA15 Kits ELISA)) and Naa10 (ARD1 (Montrer ARD1A Kits ELISA)) form a stable NatA complex which associates with ribosomes and performs co-translational N-terminal acetylation; Naa15 (NATH (Montrer NAA15 Kits ELISA)) and Naa10 (ARD1 (Montrer ARD1A Kits ELISA)) are cleaved during apoptosis resulting in decreased acetyltransferase activity
The clinical spectrum of NAA10 (Montrer ARD1A Kits ELISA).
there is no difference in lysine acetylation of substrate proteins with or without Naa10 (Montrer ARD1A Kits ELISA), suggesting that the substrates may be acetylated chemically rather than enzymatically.
Combined high expression of Naa10p, SNCG (Montrer SNCG Kits ELISA) and PRL-3 are associated with lymph node metastasis in breast cancer.
De novo missense mutations in the NAA10 (Montrer ARD1A Kits ELISA) gene cause severe non-syndromic developmental delay in males and females
human ARD1 (Montrer TRIM23 Kits ELISA) variants have different effects on cell proliferation, which may result from distinct subcellular localizations and autoacetylation activities.
Naa10 (Montrer ARD1A Kits ELISA) structure and function. [Review]
Autoacetylation of ARD1 (Montrer TRIM23 Kits ELISA) variants differentially regulates angiogenesis and cell proliferation in an isoform-specific manner.
activation of the RAGE (Montrer AGER Kits ELISA) by advanced glycation end products or other ligands suppresses NIPP1 expression in diabetic nephropathy, contributes to podocyte hypertrophy, and glomerular inflammation
NIPP1(-/-) embryos showed severely retarded growth at embryonic day 6.5 (E6.5) and were resorbed by E8.5. This early embryonic lethality was not associated with increased apoptosis but correlated with impaired cell proliferation.
NIPP1 has a role in the nuclear targeting and/or retention of PP1 (Montrer PPP1CC PLURAL_@12788@)
Required for the global trimethylation of Histone 3 at Lysine 27 and is implicated in gene silencing by enhancer of zeste homolog (EZH)2 (Montrer EZH2 Kits ELISA).
This gene, through alternative splicing, encodes three different isoforms. Two of the protein isoforms encoded by this gene are specific inhibitors of type 1 serine/threonine protein phosphatases and can bind but not cleave RNA. The third protein isoform lacks the phosphatase inhibitory function but is a single-strand endoribonuclease comparable to RNase E of E. coli. This isoform requires magnesium for its function and cleaves specific sites in A+U-rich regions of RNA.
, activator of RNA decay
, nuclear inhibitor of protein phosphatase 1
, nuclear inhibitor of protein phosphatase-1 alpha
, nuclear subunit of PP-1
, protein phosphatase 1 regulatory subunit 8
, protein phosphatase 1, regulatory (inhibitor) subunit 8
, protein phosphatase 1 regulatory inhibitor subunit 8
, protein phosphatase 1, regulatory inhibitor subunit 8
, uncharacterized protein LOC799896
, protein phosphatase 1, regulatory (inhibitor) subunit 8a
, protein phosphatase 1, regulatory subunit 8a
, protein phosphatase 1 regulatory subunit 8 S homeolog