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抗Mouse (Murine) SAG 抗体:
抗Human SAG 抗体:
抗Rat (Rattus) SAG 抗体:
Cow (Bovine) Monoclonal SAG Primary Antibody for ICC, IHC (fro) - ABIN250780
Banga, LeRoy, Suleyman, Kasp, Brown, Dumonde: Analysis of antigenic determinants of retinal S-antigen with monoclonal antibodies. in Investigative ophthalmology & visual science 1988
Show all 3 Pubmed References
The G-protein coupled receptor, DRD4, requires ARR1 and ARR4 for desensitization and internalization.
ARR4 modulates essential functions in high acuity vision and downstream cellular signaling pathways that are not fulfilled or substituted by the coexpression of ARR1, despite its high expression levels in all mouse cones.
crystal structure of a constitutively active form of human rhodopsin (显示 RHO 抗体) bound to a pre-activated form of the mouse visual arrestin, determined by serial femtosecond X-ray laser crystallography
Sag (显示 RNF7 抗体) is essential for embryonic vasculogenesis and tumor angiogenesis.
SAG (显示 RNF7 抗体) knockdown caused the accumulation of proapoptotic Bax (显示 BAX 抗体) and SARM (显示 SARM1 抗体), imbalance of Bcl-2 (显示 BCL2 抗体)/Bax (显示 BAX 抗体) in the mitochondria, induction of cytosolic cytochrome c (显示 CYCS 抗体) and activation of caspases, all of which led to disequilibrium between life and death of macrophages.
tetrameric visual arrestin 1 is a biomarker for retinal function in diabetic mice, assessed by MRI (显示 C7ORF49 抗体)
The data suggest that monomeric arrestin-1 is cytotoxic and WT arrestin-1 protects rods by forming mixed oligomers with the mutant and/or competing with it for the binding to non-receptor partners.
Findings suggest a role for Bardet-Biedl syndrome 5 (BBS5) in regulating light-dependent translocation of arrestin1 (Arr1).
Visual arrestin interaction with clathrin adaptor AP-2 (显示 TFAP2A 抗体) regulates photoreceptor survival in the vertebrate retina.
the 139-loop stabilizes basal conformation of arrestin-1 and acts as a brake, preventing its binding to non-preferred forms of rhodopsin (显示 RHO 抗体).
This is the first dominant-acting mutation identified in SAG (显示 DMBT1 抗体), a founder mutation possibly originating in Mexico several centuries ago. The phenotype is clearly adRP (显示 PLIN2 抗体) and is distinct from the previously reported phenotypes of recessive null mutations, that is, Oguchi disease and recessive RP.
Macular dysfunction can occur in Oguchi disease with the 1147delA mutation in the SAG (显示 DMBT1 抗体) gene.
NEDD4-1 (显示 NEDD4 抗体) overexpression sensitizes cancer cells to etoposide-induced apoptosis by reducing SAG (显示 DMBT1 抗体) levels through targeted degradation. SAG (显示 DMBT1 抗体) is added to a growing list of NEDD4-1 (显示 NEDD4 抗体) substrates and mediates its biological function.
Sag (显示 DMBT1 抗体) is a Kras-cooperating oncogene (显示 RAB1A 抗体) that promotes lung tumorigenesis
Based on their observed affinity for arrestin-1, P-opsin (显示 RHO 抗体) and inactive P-Rh very likely affect the physiological monomer-dimer-tetramer equilibrium of arrestin-1, and should therefore be taken into account when modeling photoreceptor function.
Compound heterozygosity of a nonsense R193X mutation and a heterozygous deletion of 3,224 bp encompassing exon 2 in the SAG (显示 DMBT1 抗体) gene is the cause of Oguchi's disease in a Chinese family.
Identification of autoantibodies specific for two retinal antigens (CRALBP (显示 RLBP1 抗体) and S-Ag) supports the concept of an autoimmunological origin of the disease.
the arrestin 1147delA, which has been known as a frequent cause of Oguchi disease, also may be related to the pathogenesis of autosomal recessive RP.
We describe a case of Oguchi disease with unusual findings caused by a putative heterozygous mutation in the SAG (显示 DMBT1 抗体) gene.
maintenance of low levels of the active monomer is the biological role of arrestin-1 self-association
Conformational changes are involved in the arrestin-rhodopsin (显示 RHO 抗体) binding interface through multiple docking modes.
K2A mutations in arrestin-1, -2, and -3 significantly reduced their binding to active phosphorhodopsin.
We hypothesize that, although arrestin requires at least a single Rho*P to bind the membrane, a single arrestin can actually interact with a pair of receptors
variant form of arrestin-1 binds rod outer segment membranes
Models suggest that the phosphorylated carboxy-terminal region of rhodopsin (显示 RHO 抗体), Rh(330-348), undergoes significant conformational changes and becomes structured upon binding to arrestin.
arrestin and p44 bind differently to different phosphorylated rhodopsin species and that this may be due to a structural difference between p44's and arrestin's basal states.
may act as a GTP/GDP-binding protein\; may play a role in signal transduction in the retina
S-antigen; retina and pineal gland (arrestin)
, -antigen; retina and pineal gland (arrestin)
, Arrestin Sb
, retinal S-antigen
, rod photoreceptor arrestin
, 48 kDa protein
, arrestin 1
, rod arrestin
, visual arrestin 1
, retinal S-antigen (48 KDa protein)
, arrestin, S-antigen