Millipore

Anti-Cystic Fibrosis Transmembrane Conductance Regulator, a.a. 1370-1380, clone M3A7

#MAB3480 · western blot

11

Citing papers

182

Combined citations

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Research areas

Cystic Fibrosis Research Advances10 Neonatal Respiratory Health Research6 Bacterial Genetics and Biotechnology2 Advanced biosensing and bioanalysis techniques2 Genetic and Kidney Cyst Diseases1 Indigenous Studies and Ecology1 Inhalation and Respiratory Drug Delivery1 Pediatric health and respiratory diseases1

Papers citing this product

1

The rescue of F508del-CFTR by elexacaftor/tezacaftor/ivacaftor (Trikafta) in human airway epithelial cells is underestimated due to the presence of ivacaftor

European Respiratory Journal·2021·49 cit.·DOI

2

Probing Conformational Rescue Induced by a Chemical Corrector of F508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutant

Journal of Biological Chemistry·2011·39 cit.·DOI

3

A novel triple combination of pharmacological chaperones improves F508del-CFTR correction

Scientific Reports·2018·38 cit.·DOI

4

Hsp70 and DNAJA2 limit CFTR levels through degradation

PLoS ONE·2019·29 cit.·DOI

5

Targeting different binding sites in the CFTR structures allows to synergistically potentiate channel activity

European Journal of Medicinal Chemistry·2020·13 cit.·DOI

6

C Terminus of Nucleotide Binding Domain 1 Contains Critical Features for Cystic Fibrosis Transmembrane Conductance Regulator Trafficking and Activation

Journal of Biological Chemistry·2010·13 cit.·DOI

7

Native CFTR codon bias controls translation rate to balance off-pathway aggregation and channel function by conformational imprinting

Scientific Reports·2025·1 cit.·DOI

8

The Avalanche Study

Revue des Maladies Respiratoires·2023·DOI

9

The Role of the Di-arginine "R553AR555" Motif in Modulating Trafficking and Function of the Major Cystic Fibrosis Causing Mutant (DeltaF508-CFTR)

TSpace (University of Toronto)·2011

10

The Role of the Di-arginine "R553AR555" Motif in Modulating Trafficking and Function of the Major Cystic Fibrosis Causing Mutant (DeltaF508-CFTR)

TSpace·2010

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