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Our data demonstrated that a specific decrease of GABARAPL1 expression in breast cancers was associated with both DNA methylation (show HELLS ELISA Kits) and histone deacetylation and that CREB-1 (show CREB1 ELISA Kits) recruitment on GABARAPL1
Androgen deprivation downregulates Gabarapl1 in an AR dependent manner, resulting in the increase of autophagy flux
Results showed that the mRNA and protein levels of GABARAPL1 and GATE-16 (show GABARAPL2 ELISA Kits) were decreased in the cerebellum of multiple system atrophy relative to controls
GABARAPL1 plays an important role in cell proliferation, invasion, and autophagic flux, as well as in mitochondrial homeostasis and cellular metabolic programs in a breast cancer cell line.
Kaplan-Meier survival analysis showed a significant association between low GABARAPL1 expression and poor prognosis of HCC (show FAM126A ELISA Kits) patients.
Lipidation of the LC3 (show MAP1LC3A ELISA Kits)/GABARAP (show GABARAP ELISA Kits) family of autophagy proteins relies on a membrane-curvature-sensing domain in Atg3 (show ATG3 ELISA Kits).
Data demonstrate that HSP90 (show HSP90 ELISA Kits) interacts and protects GABARAPL1 from its degradation by the proteasome.
analysis of specific functions of GABARAPL1 [review]
Atg8 (show GABARAPL2 ELISA Kits) interacting motif (AIM) in Stbd1 (show STBD1 ELISA Kits) is necessary for GABARAPL1 binding.
Results indicate that the presence of a tryptophan residue in the LIR (show CD300C ELISA Kits) motif increases the binding affinity of GABARAPL-1/NBR1 (show NBR1 ELISA Kits)-LIR (show CD300C ELISA Kits) complex.
Cells that lacked GABARAPs and mice that lacked Gate-16 (show GABARAPL2 ELISA Kits) alone were defective in the IFN-gamma-induced (show SAMHD1 ELISA Kits) clearance of vacuolar pathogens such as Toxoplasma. GABARAPs are uniquely required for antimicrobial host defense through cytosolic distribution of interferon (show IFNA ELISA Kits)-inducible GTPases.
study of cerebral GABARAPL1 protein expression provides insight into its role in the development and homeostasis of the mouse brain
GABARAPL1 negatively regulates Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling by mediating Dvl2 (show DVL2 ELISA Kits) degradation through the autophagy pathway.
because of its stronger binding for hKOPR, GEC1 is able to be recruited by hKOPR sufficiently without membrane association via its C-terminal modification; however, du GABARAP (show GABARAP ELISA Kits) appears to require C-terminal modifications to enhance KOPR expression.
Expression of mouse Atg8L in HEK293 cells led to cleavage of its C-terminus. (Atg8L/Apg8l)and is the fourth modifier of mammalian Atg8 (show MAP1LC3B ELISA Kits) conjugation. (ATG8L/Apg8L)
Increases cell-surface expression of kappa-type opioid receptor through facilitating anterograde intracellular trafficking of the receptor (By similarity).
GABA(A) receptor-associated protein like 1
, gamma-aminobutyric acid receptor-associated protein-like 1
, GABA(A) receptor-associated protein-like 1
, GABA(A) receptors associated protein like 3
, early estrogen-regulated protein
, glandular epithelial cell protein 1
, MDBK gamma-aminobutyric acid-receptor-associated protein
, gamma-aminobutyric acid (GABA(A)) receptor-associated protein-like 1