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PPP1R8, through alternative splicing, encodes three different isoforms. Additionally we are shipping Protein Phosphatase 1, Regulatory Subunit 8 Antibodies (97) and Protein Phosphatase 1, Regulatory Subunit 8 Kits (1) and many more products for this protein.
Showing 7 out of 9 products:
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 (show ARD1A Proteins) and that of miR (show MLXIP Proteins)-342-5p and miR (show MLXIP Proteins)-608 .
Human Naa15 (NATH (show NAA15 Proteins)) and Naa10 (ARD1 (show ARD1A Proteins)) form a stable NatA complex which associates with ribosomes and performs co-translational N-terminal acetylation; Naa15 (NATH (show NAA15 Proteins)) and Naa10 (ARD1 (show ARD1A Proteins)) are cleaved during apoptosis resulting in decreased acetyltransferase activity
The clinical spectrum of NAA10 (show ARD1A Proteins).
there is no difference in lysine acetylation of substrate proteins with or without Naa10 (show ARD1A Proteins), suggesting that the substrates may be acetylated chemically rather than enzymatically.
Combined high expression of Naa10p, SNCG (show SNCG Proteins) and PRL-3 are associated with lymph node metastasis in breast cancer.
De novo missense mutations in the NAA10 (show ARD1A Proteins) gene cause severe non-syndromic developmental delay in males and females
human ARD1 (show TRIM23 Proteins) variants have different effects on cell proliferation, which may result from distinct subcellular localizations and autoacetylation activities.
Naa10 (show ARD1A Proteins) structure and function. [Review]
Autoacetylation of ARD1 (show TRIM23 Proteins) variants differentially regulates angiogenesis and cell proliferation in an isoform-specific manner.
activation of the RAGE (show AGER Proteins) 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 (show PPP1CC Proteins)
Required for the global trimethylation of Histone 3 at Lysine 27 and is implicated in gene silencing by enhancer of zeste homolog (EZH)2 (show EZH2 Proteins).
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.
ARD1 homolog A, N-acetyltransferase
, N-acetyltransferase ARD1, human homolog of
, N-alpha-acetyltransferase 10
, N-alpha-acetyltransferase 10, NatA catalytic subunit
, N-terminal acetyltransferase complex ARD1 subunit homolog A
, nuclear inhibitor of protein phosphatase 1
, protein phosphatase 1 regulatory inhibitor subunit 8
, protein phosphatase 1, regulatory (inhibitor) subunit 8
, protein phosphatase 1, regulatory inhibitor subunit 8
, RNase E
, activator of RNA decay
, nuclear inhibitor of protein phosphatase-1 alpha
, nuclear subunit of PP-1
, protein phosphatase 1 regulatory subunit 8
, uncharacterized protein LOC799896