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Synonyms
D10S64 antibody; D10S65 antibody; D10S66 antibody; Interphotoreceptor retinoid binding protein antibody; Interphotoreceptor retinoid-binding protein antibody; Interstitial retinol binding protein antibody; Interstitial retinol-binding protein antibody; IRBP antibody; RBP 3 antibody; rbp3 antibody; RBPI antibody; RET3_HUMAN antibody; Retinol binding protein 3 antibody; Retinol binding protein 3 interstitial antibody; Retinol-binding protein 3 antibody; RP66 antibody
IRBP (Interphotoreceptor Retinoid-Binding Protein) plays a crucial role in the visual cycle by transporting 11-cis and all-trans retinoids between the retinol isomerase in the retinal pigment epithelium and the visual pigments within the photoreceptor cells of the retina.
Gene References Into Functions
This report is the first to document retinal dystrophy in children caused by homozygous nonsense RBP3 mutations, highlighting the essential role of IRBP in normal eye development and visual function. PMID: 25766589
CMPK1 and RBP3 are associated with corneal curvature in Asian populations. PMID: 24963161
Our research revealed that most patients with macular telangiectasia-2 possess retinal autoantibodies, with the most prevalent being directed against AGL, RBP3, and CK-B. PMID: 23882694
Secretory defect and cytotoxicity are potential disease mechanisms for the retinitis pigmentosa (RP)-associated interphotoreceptor retinoid-binding protein (IRBP). PMID: 23486466
The mouse retina facilitates cone dark adaptation eightfold faster than the retinal pigment epithelium. However, complete cone recovery requires both visual cycles. PMID: 21613504
Reduced production of IRBP is an early event in the human diabetic retina and is linked to retinal neurodegeneration. PMID: 19823802
Studies suggest that IRBP and S-Ag can initiate innate and, in susceptible individuals, adaptive immune response by attracting iDCs and T and B cells expressing CXCR3 and CXCR5 PMID: 15713799
Analysis of IRBP proteolysis serves as a useful biomarker for uveitis PMID: 18266969
Mutations in RBP3 are an infrequent cause of autosomal recessive retinitis pigmentosa. PMID: 19074801
In interphotoreceptor retinoid-binding protein transgenic mice, cone dysfunction appears to stem from abnormal trafficking of cone opsins due to impaired delivery of all-transretinaldehyde chromophore in the absence of IRBP. PMID: 19193895
Secreted, extracellular space, extracellular matrix, interphotoreceptor matrix. Note=Interphotoreceptor matrix that permeates the space between the retina and the contiguous layer of pigment epithelium cells.
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