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Recombinant Rat CFTR Protein

Cat.No. : CFTR-1357R
Product Overview : Recombinant Rat CFTR full length or partial length protein was expressed.
  • Specification
  • Gene Information
  • Related Products
Source : Mammalian Cells
Species : Rat
Tag : His
Form : Liquid or lyophilized powder
Endotoxin : < 1.0 EU per μg of the protein as determined by the LAL method.
Purity : >80%
Notes : This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
Storage : Store it at +4 ºC for short term. For long term storage, store it at -20 ºC~-80 ºC.
Storage Buffer : PBS buffer
Gene Name : Cftr cystic fibrosis transmembrane conductance regulator [ Rattus norvegicus ]
Official Symbol : CFTR
Gene ID : 24255
mRNA Refseq : NM_031506.1
Protein Refseq : NP_113694.1
MIM :
UniProt ID : P34158

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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Q&As (5)

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Is there any gene therapy or medications targeting CFTR protein for CF treatment? 10/22/2022

Yes, there are medications like Ivacaftor, Lumacaftor, and Tezacaftor that target specific CFTR mutations to improve CFTR function. Gene therapy approaches are also being developed.

Are there different types of CFTR mutations, and do they have varying clinical implications? 03/13/2021

Yes, there are various types of CFTR mutations, some of which are associated with milder or more severe forms of CF, depending on the specific mutation.

Are there ongoing clinical trials and research related to CFTR protein and CF treatment? 02/11/2021

Yes, there are numerous clinical trials and research studies focusing on CFTR-targeted therapies and novel approaches for treating cystic fibrosis.

Can CFTR protein-related therapies benefit individuals with non-CF conditions? 07/18/2019

Yes, some CFTR-targeted therapies may have potential applications in conditions involving mucus secretion, like chronic bronchitis and bronchiectasis.

What are the current clinical treatments for CF patients related to CFTR protein dysfunction? 02/04/2019

Current treatments aim to alleviate symptoms and improve the quality of life for CF patients, including therapies to reduce mucus thickness, antibiotics for lung infections, and airway clearance techniques.

Customer Reviews (3)

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Reviews
12/25/2020

    the CFTR protein's exceptional quality, coupled with the manufacturer's outstanding technical support, ensures that it fulfills my experimental needs with utmost precision and efficacy.

    05/08/2019

      the CFTR protein is an exceptional tool for investigating the intricate mechanisms and pathogenesis of amyloid-related diseases.

      01/09/2016

        Their collaboration during trial design and data analysis enhances the reliability and significance of my research findings.

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