Related Experiment Video

Updated: Aug 11, 2026

Functional Reconstitution and Channel Activity Measurements of Purified Wildtype and Mutant CFTR Protein
09:59

Functional Reconstitution and Channel Activity Measurements of Purified Wildtype and Mutant CFTR Protein

Published on: March 9, 2015

Using a cysteine-less mutant to provide insight into the structure and mechanism of CFTR

Tip W Loo1, David M Clarke

  • 1Department of Medicine and Biochemistry, University of Toronto, Canada.

The Journal of Physiology
|February 25, 2006
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein Expressed in Saccharomyces cerevisiae
15:12

Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein Expressed in Saccharomyces cerevisiae

Published on: May 10, 2014

Functional Site-Directed Fluorometry in Native Cells to Study Skeletal Muscle Excitability
12:26

Functional Site-Directed Fluorometry in Native Cells to Study Skeletal Muscle Excitability

Published on: June 2, 2023

Related Experiment Videos

Last Updated: Aug 11, 2026

Functional Reconstitution and Channel Activity Measurements of Purified Wildtype and Mutant CFTR Protein
09:59

Functional Reconstitution and Channel Activity Measurements of Purified Wildtype and Mutant CFTR Protein

Published on: March 9, 2015

Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein Expressed in Saccharomyces cerevisiae
15:12

Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein Expressed in Saccharomyces cerevisiae

Published on: May 10, 2014

Functional Site-Directed Fluorometry in Native Cells to Study Skeletal Muscle Excitability
12:26

Functional Site-Directed Fluorometry in Native Cells to Study Skeletal Muscle Excitability

Published on: June 2, 2023

Related Concept Videos

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...

Articles linked to this work by shared authors, journal, and citation graph.

Agile Comprehensive Care: A Pragmatic Trial of a Systemic Intervention for High Utilizers of Emergency Departments.

Healthcare (Basel, Switzerland)·2025

Measuring postnatal demoralisation: adaptation of the Demoralisation Scale-II (DS-II) for postnatal use.

Journal of reproductive and infant psychology·2018

Symptom attribution and treatment seeking in Australian veterans.

Journal of health psychology·2018

Medical student psychological distress and academic performance.

Medical teacher·2018

A short cross-linker activates human P-glycoprotein missing a catalytic carboxylate.

Biochemical pharmacology·2017

Thiol-reactive drug substrates of human P-glycoprotein label the same sites to activate ATPase activity in membranes or dodecyl maltoside detergent micelles.

Biochemical and biophysical research communications·2017

The influence of force on the encoding and perception of affective touch.

The Journal of physiology·2026

β-hydroxy-β-methylbutyrate improves fast-twitch muscle function, histopathology and mitochondrial respiration in the D2.mdx dystrophic mouse.

The Journal of physiology·2026

Disrupted bilateral co-ordination of soleus motor units during early subacute stroke rehabilitation.

The Journal of physiology·2026

Myostatin-dependent detrusor remodelling mediates contractility impairment in diabetic rats' bladder - a maximal elastance analysis.

The Journal of physiology·2026

P2X3 receptor antagonism improves hindlimb blood flow during exercise in a conscious ovine model of hypertensive heart failure with preserved ejection fraction.

The Journal of physiology·2026

Early kidney injury occurs in the absence of detectable perirenal adipose tissue remodelling in the Munich Wistar Frömter rat model of chronic kidney disease.

The Journal of physiology·2026

[Severe dysphagia after traumatic cervical cord injury: improved by combined surgery of subglottic laryngeal closure and cricopharyngeal myotomy].

Rinsho shinkeigaku = Clinical neurology·2026

[Medium optimization and fermentation regulation strategies for enhancing CO2 conversion to acetic acid coupled with H2 by Clostridium ljungdahlii].

Sheng wu gong cheng xue bao = Chinese journal of biotechnology·2026

A novel class of conserved sucrose-phosphate phosphatases highlights the diversity of cyanobacterial sucrose metabolism.

Bioresource technology·2026

From biomass side-product to nano-therapeutics: Characterization and anti-colitis efficacy of carbon dots originating from Nelumbinis Rhizomatis Nodus Carbonisatus.

Colloids and surfaces. B, Biointerfaces·2026

Minimally Invasive Strip Craniectomy-Extended (MIS-E): A Technical Modification for Treatment of Sagittal Craniosynostosis.

Pediatric neurosurgery·2026

William Athol McElmoyle and the Forgotten Shield: Rediscovering an Early Principle of Safe Cholecystectomy.

Journal of the American College of Surgeons·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us