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The protein encoded by RLBP1 is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. Zusätzlich bieten wir Ihnen Retinaldehyde Binding Protein 1 Proteine (7) und Retinaldehyde Binding Protein 1 Kits (5) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal RLBP1 Primary Antibody für ICC, IF - ABIN441762
Johnson, Bachman, Gilles, Cross, Stelzig, Resch, Marmorstein, Pulido, Marmorstein: Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a Novel BEST1 Mutation. in Investigative ophthalmology & visual science 2015
Cralbp b expression in Muller cells of the retina is essential for cone vision and provides evidence that both the canonical and the alternative visual cycle depend on the same type of retinoid-binding protein.
we provide evidence for an allosteric modulation of the enzymatic activity by 11-cis (zeige CISH Antikörper) retinoids. This regulation is independent from cellular retinaldehyde-binding protein (CRALBP), the major cis (zeige CISH Antikörper)-retinoid binding protein.
We conclude that the expression of Rlbp1 and Rdh5 (zeige RDH5 Antikörper) critically depends on functional Mitf (zeige MITF Antikörper) in the RPE (zeige RPE Antikörper) and suggest that MITF (zeige MITF Antikörper) has an important role in controlling retinoid processing in the RPE (zeige RPE Antikörper).
Different mutations in RLBP1 are correlated with quite different morphological and functional characteristics outlines the complexity of the protein.
RLBP1 gene is upregulated in patients with reactive retinal astrocytic tumors.
Patients with retinitis punctata albescens (RPA) show variable degrees of foveal cone death, even at an early stage. This finding has implications for future treatment.
The two RLBP1 genotypes presented a phenotypical and electrophysiological expression of progressive retinal disease similar to that previously described in homozygotes for the c.700C>T (p.R234W) RLBP1 mutation.
The clinical characteristics of a Japanese patient with a homozygous R234W mutation in RLBP1 are very similar to that of Swedish patients with Bothnia dystrophy.
Identification of autoantibodies specific for two retinal antigens (CRALBP and S-Ag (zeige SAG Antikörper)) supports the concept of an autoimmunological origin of the disease.
The R234W mutation reveals impaired 11-cis (zeige CISH Antikörper)-retinal release through stabilization of the ligand complex.
mutations in RLBP1 are responsible for fundus albipunctatus in the affected individuals of these consanguineous Pakistani families.
results identify Muller cell CRALBP as a key component of the retinal visual cycle and demonstrate that this pathway is important for maintaining normal cone-driven vision and accelerating cone dark adaptation.
CRALBP is a direct downstream target of Pax6 (zeige PAX6 Antikörper).
Potential role for Rlbp1 and Syntaxin 12 (zeige STX12 Antikörper) in ethanol preference in mice, a conclusion supported by the location of these genes in quantitative trait loci (QTL).
Regulatory elements in a restricted region of the Rlbp1 gene are sufficient to drive GFP expression in vivo.
The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens.
retinaldehyde binding protein 1
, retinaldehyde-binding protein 1
, cellular retinaldehyde-binding protein
, cellular retinaldehyde-binding protein-1