ARD1 Homolog, N-Acetyltransferase (ARD1A) ELISA试剂盒

N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. 再加上,我们可以发ARD1 Homolog, N-Acetyltransferase 抗体 (51)ARD1 Homolog, N-Acetyltransferase 蛋白 (9)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
ARD1A 8260 P41227
小鼠 ARD1A ARD1A 56292 Q9QY36
大鼠 ARD1A ARD1A 363518  
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Human ARD1 Homolog, N-Acetyltransferase (ARD1A) interaction partners

  1. In combination with acetylation assays, the HypK N-terminal region is identified as a negative regulator of the NatA acetylation activity

  2. ARD1-mediated Hsp70 (显示 HSP70 ELISA试剂盒) acetylation is a regulatory mechanism that temporally balances protein refolding/degradation in response to stress

  3. Negative regulation of Naa10 towards NTN1 (显示 NTN1 ELISA试剂盒) and its receptor UNC5B (显示 UNC5B ELISA试剂盒) were also detected upon treatment of all-trans retinoid acid, which was often used to induce morphological differentiation.

  4. A novel de novo NAA10 c.332 T>G p.(Val111Gly) missense variant was detected in a girl with mild/moderate non-syndromic intellectual disability. NAA10 V111G displayed reduced monomeric NAT (显示 BRD2 ELISA试剂盒) activity and stability, but intact NatA-mediated NAT (显示 BRD2 ELISA试剂盒) activity.

  5. Expression of ARD1 increases levels of androgen receptor (显示 AR ELISA试剂盒) acetylation and androgen receptor (显示 AR ELISA试剂盒)-HSP90 (显示 HSP90 ELISA试剂盒) dissociation in a dose dependent manner.

  6. Study reports on a total of 12 affected females with four different de novo missense mutations in NAA10 and one inherited mutation in a familial case due to germline mosaicism, thus further expanding themutational and clinical spectrum associated with NAA10 related N-terminal-acetyltransferase deficiency.

  7. The results observed an inverse correlation between the expression of NAA10 and that of miR-342-5p and miR-608 .

  8. Human Naa15 (NATH) and Naa10 (ARD1) form a stable NatA complex which associates with ribosomes and performs co-translational N-terminal acetylation; Naa15 (NATH) and Naa10 (ARD1) are cleaved during apoptosis resulting in decreased acetyltransferase activity

  9. The clinical spectrum of NAA10.

  10. there is no difference in lysine acetylation of substrate proteins with or without Naa10, suggesting that the substrates may be acetylated chemically rather than enzymatically.

Mouse (Murine) ARD1 Homolog, N-Acetyltransferase (ARD1A) interaction partners

  1. Negative regulation of Naa10 towards NTN1 (显示 NTN1 ELISA试剂盒) and its receptor UNC5B (显示 UNC5B ELISA试剂盒) were also detected upon treatment of all-trans retinoid acid, which was often used to induce morphological differentiation.

  2. The lethal Ogden syndrome-associated mutation of Naa10p disrupts its binding to the imprinting control region of H19 (显示 NCKAP1 ELISA试剂盒) and Dnmt1 (显示 DNMT1 ELISA试剂盒) recruitment.

  3. NAA10 acts as a guard ensuring balanced osteogenesis by fine-tuning Runx2 (显示 RUNX2 ELISA试剂盒) signalling in a feedback manner.

  4. ARD1 has a crucial role in the cellular response to oxidative stress as a bona fide regulator of MSRA (显示 MSR1 ELISA试剂盒).

  5. mARD1A(225) may be a novel upstream target that blocks VEGFA (显示 VEGFA ELISA试剂盒) expression and tumor-related angiogenesis.

  6. Biochemical analysis demonstrated that mNAT1 and its evolutionarily conserved co-subunit, mARD1, assemble to form a functional acetyltransferase.

  7. Mouse ortholog (225) of ARD1 strongly decreased the level of hypoxia inducible factor (HIF)-1 alpha (显示 HIF1A ELISA试剂盒) and increased the extent of acetylation, whereas mARD1(235) variants had a much weaker effect on HIF-1 alpha (显示 HIF1A ELISA试剂盒) stability and acetylation.

  8. These results indicate that ARD1(235) and ARD1(225) isoforms may have different activities and function in different subcellular compartments of mammalian cells.

ARD1 Homolog, N-Acetyltransferase (ARD1A) 抗原简介

Antigen Summary

N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants.

Gene names and symbols associated with ARD1A

  • N(alpha)-acetyltransferase 10, NatA catalytic subunit (NAA10) 抗体
  • N(alpha)-acetyltransferase 10, NatA catalytic subunit (Naa10) 抗体
  • 2310039H09Rik 抗体
  • Ard1 抗体
  • Ard1a 抗体
  • DXS707 抗体
  • NATD 抗体
  • RGD1565315 抗体
  • Te2 抗体

Protein level used designations for ARD1A

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 , alpha-N-acetyltransferase 1A , natA catalytic subunit , N-acetyltransferase ARD1 , N(alpha)-acetyltransferase 10, NatA catalytic subunitNalpha acetyltransferase 10 , N-acetyltransferase ARD1 homolog , Nalpha acetyltransferase 10

GENE ID SPECIES
8260 Homo sapiens
613636 Bos taurus
100328748 Oryctolagus cuniculus
56292 Mus musculus
363518 Rattus norvegicus
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