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Plays a role in autophagy. Additionally we are shipping ATG9A Proteins (5) and many more products for this protein.
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Chicken Polyclonal ATG9A Primary Antibody for ICC, IF - ABIN189269
Chen, Luo, Dong, Tan, Yang, Feng, Wu, Li, Wang: CD133/prominin-1-mediated autophagy and glucose uptake beneficial for hepatoma cell survival. in PLoS ONE 2013
Show all 14 Pubmed References
Human Polyclonal ATG9A Primary Antibody for IF, IHC (p) - ABIN388528
Baehrecke: Autophagy: dual roles in life and death? in Nature reviews. Molecular cell biology 2005
Show all 7 Pubmed References
Contrary to its normal trafficking between plasma membrane, intracellular organelles and autophagic membranes, ATG9A concentrates in transferrin receptor-positive juxtanuclear recycling endosomes in SMPD1 (show SMPD1 Antibodies)-deficient cells.
Findings show for this first time that ATG9A loss in trastuzumab resistant cells allowed Her2 (show ERBB2 Antibodies) to escape from lysosomal targeted degradation through K63 poly-ubiquitination via c-Cbl (show CBL Antibodies).
phosphorylation of mATG9 at Tyr8 by Src (show SRC Antibodies) and at Ser14 by ULK1 (show ULK1 Antibodies) functionally cooperate to promote interactions between mATG9 and the AP1 (show FOSB Antibodies)/2 complex.
In these Rab1B (show RAB1B Antibodies)-depleted cells, ATG9A accumulated in intermediate membrane structures at autophagosome formation sites. These results indicate that Rab1B (show RAB1B Antibodies) is involved in regulating the proper development of autophagosomes.
we focus on the contributions of the plasma membrane to autophagosome biogenesis governed by ATG16L1 (show ATG16L1 Antibodies) and ATG9A trafficking, and summarize the physiological and pathological implications of this macroautophagy route, from development and stem cell fate to neurodegeneration and cancer.
the C-terminal glycine of human ATG9A is required for its transport from the endoplasmic reticulum to the Golgi apparatus
these findings provide new insights into the intracellular pathways followed by ATG9A to reach different subcellular compartments, and into the intramolecular determinants that drive the sorting of this protein.
Results suggest that quinocetone stimulates the MRLC-mediated mAtg9 trafficking, which is critical for autophagosome formation, via the ATF6 (show ATF6 Antibodies) upregulated expression of DAPK1 (show DAPK1 Antibodies).
This study highlights the transcriptional inactivation mechanisms of ATG2B, ATG4D (show ATG4D Antibodies), ATG9A and ATG9B (show ATG9B Antibodies) promoter methylation status and the possible origin of autophagy signal pathway repression in invasive ductal carcinomas.
Importantly, TBC1D14 (show TBC1D14 Antibodies) and TRAPPIII regulate ATG9 trafficking independently of ULK1 (show ULK1 Antibodies).
the trafficking of Atg9A through the recycling endosomes is an essential step for autophagosome formation.
Atg9a(-/-) fetal mice from pregnant dams heterozygous for both knockout alleles of Atg9a and p57(Kip2 (show CDKN1C Antibodies)) are more susceptible to hypertensive stress than fetuses with intact autophagic machinery.
Atg9a expression is required for neural stem cell differentiation.
Knockdown of Atg9a resulted in enhanced stimulator of IFN genes-mediated production of IFN-beta (show IFNB1 Antibodies) by aged macrophages
Both AMPK (show PRKAA1 Antibodies) and ULK1 (show ULK1 Antibodies) regulate localization of a critical component of the phagophore, ATG9.
In the initial steps of Parkin (show PARK2 Antibodies)-mediated mitophagy, the structures containing the ULK1 (show ULK1 Antibodies) complex and Atg9A are independently recruited to depolarized mitochondria.
STING co-localizes with the autophagy proteins, microtubule-associated protein (show SPAG5 Antibodies) 1 light chain 3 (LC3 (show MAP1LC3A Antibodies)) and autophagy-related gene 9a (Atg9a), after dsDNA stimulation.
Atg9Ap may be involved in autophagosome formation in the ER and axon terminals of neurons, the TGN (show TG Antibodies), and lysosomes/late endosomes.
Plays a role in autophagy. Cycles between a juxta- nuclear trans-Golgi network compartment and late endosomes. Nutrient starvation induces accumulation on autophagosomes. Starvation-dependent trafficking requires ULK1, ATG13 and FAM48A (By similarity).
ATG9 autophagy related 9 homolog A
, autophagy protein 9
, ATG9 autophagy related 9 homolog A (S. cerevisiae)
, autophagy-related protein 9A
, Autophagy-related protein 9A
, APG9-like 1
, APG9 autophagy 9-like 1
, autophagy 9-like 1 protein
, autophagy-related 9-like 1
, autophagy-related 9A