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Plays a role in autophagy. Additionally we are shipping ATG9A Proteins (5) and ATG9A Kits (4) and many more products for this protein.
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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
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Human Polyclonal ATG9A Primary Antibody for EIA, IHC (p) - ABIN1449609
Lum, DeBerardinis, Thompson: Autophagy in metazoans: cell survival in the land of plenty. in Nature reviews. Molecular cell biology 2005
Show all 7 references for ABIN1449609
Human Polyclonal ATG9A Primary Antibody for IHC (p), WB - ABIN388527
Greenberg: Degrade or die: a dual function for autophagy in the plant immune response. in Developmental cell 2005
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Cow (Bovine) Polyclonal ATG9A Primary Antibody for WB - ABIN2782088
Olsen, Blagoev, Gnad, Macek, Kumar, Mortensen, Mann: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. in Cell 2006
Human Polyclonal ATG9A Primary Antibody for EIA, IF - ABIN783751
Gozuacik, Kimchi: Autophagy as a cell death and tumor suppressor mechanism. in Oncogene 2004
Importantly, TBC1D14 (show TBC1D14 Antibodies) and TRAPPIII regulate ATG9 trafficking independently of ULK1 (show ULK1 Antibodies).
These two steps are essential for the maturation of small single-membrane autophagic precursors containing ATG16L1 (show ATG16L1 Antibodies) and mATG9 proteins into double-membrane autophagosomes
D620N mutation in VPS35 (show vps35 Antibodies) restricts WASH complex recruitment to endosomes, inhibiting autophagy. The autophagy defects can be explained, at least in part, by abnormal trafficking of the autophagy protein ATG9A.
Data found that the interaction between 14-3-3 zeta (show YWHAZ Antibodies) and Atg9A is mediated by phosphorylation at Ser761.
TBC1D5 (show TBC1D5 Antibodies) and the AP2 complex (show AP2B1 Antibodies) are important novel regulators of the rerouting of ATG9-containing vesicular carriers toward sites of autophagosome formation.
miR (show MLXIP Antibodies)-29b mRNA, MAPK10 (show MAPK10 Antibodies) protein expression, and ATG9A protein expression are closely related to chemosensitivity of ovarian carcinoma.
the presence of ATG9A in the cytoplasm of tumor cells may be an independent biomarker for disease recurrence and survival in patients with oral squamous cell carcinoma
ATG9A was found by co-immunoprecipitation to interact with FAM48A/p38IP (show SUPT20H Antibodies)/q8NEM7.2.
These findings suggest that Bif-1 (show ZBTB24 Antibodies) acts as a critical regulator of Atg9 puncta formation presumably by mediating Golgi fission for autophagosome biogenesis during starvation.
mAtg9 trafficking through multiple organelles, including recycling endosomes, is essential for the initiation and progression of autophagy
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