All Trans Retinol

All-trans retinol is the alcohol form of vitamin A, a lipid-soluble molecule essential for vision, epithelial maintenance, growth, and development. In cells, it can be esterified for storage or oxidized to all-trans retinaldehyde and then to all-trans retinoic acid, which regulates gene expression by activating nuclear retinoic acid receptors; in the visual cycle, related retinoid transformations support regeneration of light-sensitive pigments. Studying all-trans retinol helps explain vitamin A metabolism, retinal physiology, and retinoid signaling in biology. Its pathways also inform research on deficiency, embryonic development, skin biology, and therapeutic retinoid design.

All Trans Retinol - Related Videos

Research

JoVE Journal - Biology

Real-time Analyses of Retinol Transport by the Membrane Receptor of Plasma Retinol Binding Protein

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Cited by 11 •

2013

Here we describe an optimized technique to produce high-quality vitamin A/RBP complex and two real-time monitoring techniques to study vitamin A transport by STRA6, the RBP receptor.

Trans-Spinal Direct Current Stimulation of a Rat's Spinal Motoneuron

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2025

This video describes the in vivo intracellular recording of rat motoneurons under trans-spinal direct current stimulation. The protocol describes how to measure membrane properties and record the rhythmic firing of motoneurons before, during, and after anodal or cathodal polarization of the spinal cord.

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation

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Cited by 19 •

2013

We describe a valuable diagnostic assay that could potentially be used to decide the withdrawal of immunosuppression after transplant without elevated risk of graft rejection. The assay uses the principles of Delayed Type Hypersensitivity and provides accurate assessment of both donor specific effector and regulatory immune responses mounted by recipients.

Education

JoVE Core - Organic Chemistry

Disubstituted Cyclohexanes: cis-trans Isomerism

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2023

Depending upon the different spatial orientation of the substituents, the disubstituted cycloalkanes exhibit two types of stereoisomers. The cis isomers have the substituents on the same side of the ring, whereas the trans isomers have the substituents on the opposite sides. These stereoisomers exhibit different physical properties and cannot be interconverted without breaking the carbon-carbon bonds. In cyclohexane, the substituents can occupy different positions generating distinct isomers.

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity

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Cited by 12 •

2018

We present a technique for localized administration of drugs through the trans-tympanic route into the cochlea. Drug delivery through this route would not interfere with the anti-cancer efficacy of the chemotherapeutic drugs such as cisplatin.

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