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Human Polyclonal ATG7 Primary Antibody pour IF, IHC (p) - ABIN388522
Baehrecke: Autophagy: dual roles in life and death? dans Nature reviews. Molecular cell biology 2005
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Human Polyclonal ATG7 Primary Antibody pour ICC, IF - ABIN269462
Park, Lee, Kim, Lee, Lee, Kim, Jang, Choi, Kwon, Kim: A human scFv antibody against TRAIL receptor 2 induces autophagic cell death in both TRAIL-sensitive and TRAIL-resistant cancer cells. dans Cancer research 2007
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Human Polyclonal ATG7 Primary Antibody pour EIA, WB - ABIN118061
Aoki, Kobayashi, Tanida, Hatano, Komori, Matsumoto, Nishioka, Uemura: [A difficult case of esophageal and gastric double cancer with pleural and pericardial effusion following chemo-radiotherapy (CRT)] dans Gan to kagaku ryoho. Cancer & chemotherapy 2008
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Human Polyclonal ATG7 Primary Antibody pour IHC (p), WB - ABIN4282130
Lee, Chen, Su, Chueh: Sirtuin 1 (SIRT1) Deacetylase Activity and NAD⁺/NADH Ratio Are Imperative for Capsaicin-Mediated Programmed Cell Death. dans Journal of agricultural and food chemistry 2015
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Human Polyclonal ATG7 Primary Antibody pour IHC (p), WB - ABIN388521
Lum, DeBerardinis, Thompson: Autophagy in metazoans: cell survival in the land of plenty. dans Nature reviews. Molecular cell biology 2005
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Human Monoclonal ATG7 Primary Antibody pour CyTOF, FACS - ABIN4900316
Bernard, Dieudé, Yang, Hamelin, Underwood, Hébert: Autophagy fosters myofibroblast differentiation through MTORC2 activation and downstream upregulation of CTGF. dans Autophagy 2015
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Human Monoclonal ATG7 Primary Antibody pour WB - ABIN387793
Metzger, Saukko, Van Che, Tong, Puder, Riess, Nguyen: Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7. dans Human genetics 2010
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Human Polyclonal ATG7 Primary Antibody pour IF, IHC (p) - ABIN388523
Greenberg: Degrade or die: a dual function for autophagy in the plant immune response. dans Developmental cell 2005
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Human Polyclonal ATG7 Primary Antibody pour IHC (p), WB - ABIN388520
Levine: Eating oneself and uninvited guests: autophagy-related pathways in cellular defense. dans Cell 2005
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miR (Montrer MLXIP Anticorps)-106a suppresses tumor cells death in colorectal cancer through targeting ATG7.
PSMD10/gankyrin (Montrer PSMD10 Anticorps) has a role in inducing autophagy to promote tumor progression through cytoplasmic interaction with ATG7 and nuclear transactivation of ATG7 expression
the ATG5 (Montrer ATG5 Anticorps)-ATG7-NCOA4 (Montrer NCOA4 Anticorps) autophagic pathway has a role in ferroptosis
knockdown of autophagy genes ATG5 (Montrer ATG5 Anticorps) or ATG7 resulted in reduced hematopoietic stem/progenitor cell frequencies in vitro as well as in vivo.
Nine of the 32 (28.1%) iCCA (Montrer PRRT2 Anticorps) patients had gene mutations at chromosome 3p, totaling 11 mutations across five genes. Those included five (15.6%) BAP1 (Montrer RNF2 Anticorps) mutations, two each (6.3%) of CACNA2D3 (Montrer CACNA2D3 Anticorps) and RASSF1 (Montrer RASSF1 Anticorps) mutations, and one each (3.1%) of ATG7 and PLCD1 (Montrer PLCD1 Anticorps) mutations. Six (18.8%) cases had concurrent loss of chromosome 3p and gene mutations.
knockdown of ATG7 results in decreased glycolysis and increased flux of labeled carbons through the mitochondrial tricarboxylic acid cycle.
SNP rs11706903 in ATG7 was not associated with systemic lupus erythematosus I Chinese Han population.
low serum ATG7 is associated with ulcerative colitis
The U2AF35 (Montrer U2AF1 Anticorps)(S34F) mutation alters interaction with CFIm59 (Montrer CPSF7 Anticorps), leading to increased use of a distal cleavage and polyadenylation site in the ATG7 pre-mRNA, decreasing levels of ATG7 protein and defective autophagy, ultimately leading to transformation.
the inhibition of Atg7 appears to be a valid strategy to enhance chemosensitivity, and it could indeed improve outcomes in acute myeloid leukemia (Montrer BCL11A Anticorps) therapy.
A thiol-dependent process is being reported that may account for impaired autophagy during aging. This is through direct oxidation of key autophagy-related (Atg) proteins Atg3 (Montrer ATG3 Anticorps) and Atg7.
Atg7 regulates IL-6 (Montrer IL6 Anticorps) production via NF-kappaB (Montrer NFKB1 Anticorps) to modulate brain angiogenesis. These findings established Atg7 as a novel regulatory molecule contributing to angiogenesis in the brain.
Autophagy deficiency induced by RPE (Montrer RPE Anticorps)-specific deletion of Atg5 (Montrer ATG5 Anticorps) or Atg7 predisposes but does not necessarily drive the development of AMD (Montrer AMD1 Anticorps)-like phenotypes or retinal degeneration.
ATG7 has a role in autophagy deficiency in macrophages that may contribute to the progression of metabolic syndrome associated with lipid injury and colitis
ATG proteins ATG5 (Montrer ATG5 Anticorps) and ATG7 may be required for phagosome maturation under some conditions, but are not universally required for this process
Autophagy and tumorigenesis were not increased in Atg7(+/-) mice kept in social isolation and fed OID. Thus, social isolation may increase breast cancer risk by inducing autophagy, independent of changes in body weight.
ATG7, but not ATG13 (Montrer ATG13 Anticorps) or ULK1 (Montrer ULK1 Anticorps) has a role in functional autophagy in glioblastoma development
Atg7 is critical for the survival of midbrain dopaminergic (mDA) neurons in physiological condition. Atg7 is up-regulated when exposed to MPTP (Montrer PTPN2 Anticorps), but unlike in the control mice, chronic MPTP (Montrer PTPN2 Anticorps) treatment did not lead to loss of mDA neurons in Atg7 conditional knockout mice. These results suggest that excessive Atg7-involved autophagy in the pathological condition has deleterious effects on the survival of mDA neurons.
It shows that AMBRA1 (Montrer AMBRA1 Anticorps), but not ATG7, plays a role in TCR-mediated control of glycolytic factors and mitochondrial mass, while both AMBRA1 (Montrer AMBRA1 Anticorps) and ATG7 are required for autolysosome formation.
This gene was identified based on homology to Pichia pastoris GSA7 and Saccharomyces cerevisiae APG7. In the yeast, the protein appears to be required for fusion of peroxisomal and vacuolar membranes. The protein shows homology to the ATP-binding and catalytic sites of the E1 ubiquitin activating enzymes.
autophagy-related protein 7
, Autophagy-related protein 7
, ATG7 autophagy related 7 homolog
, ATG12-activating enzyme E1 ATG7
, ubiquitin activating enzyme E1-like protein
, ubiquitin-activating enzyme E1-like protein
, ubiquitin-like modifier-activating enzyme ATG7
, autophagy-related 7
, autophagy related 7 homolog
, potential E1-like Atg12p-Atg5p conjugation enzyme Atg7