Cystic fibrosis transmembrane conductance regulator (CFTR) antibody

ATP-binding cassette sub-family C member 7
Channel conductance-controlling ATPase
cAMP-dependent chloride channel
Gene name: CFTR, ABCC7, ABC35, CF/MRP, MRP7, TNR-CFTR, dJ760C5.1
As low as €267.30
In stock
Defects in CFTR are the cause of cystic fibrosis (CF) also known as mucoviscidosis.
More Information
ID Covalab pab0716-P
Product type Primary antibodies
Clonality Polyclonal antibody
Raised in Rabbit
Immunogen Synthetic peptide derived from Nter domain of human CFTR protein.
Activity cross reaction Reacts with human CFTR. May cross-react with mouse CFTR due to sequence homology.
Species Hu
Labelling None
Form Purified (protein A)
Preservative None
Storage instructions Lyophilized powder stable for a minimum of 2 years at -20°C.
Store reconstituted antibodies at +4°C.
For extended periods store in aliquots at -20°C.
Antibodies are guaranteed for 6 month from date of receipt.
Target Cystic fibrosis transmembrane conductance regulator (CFTR)
Uniprot ID P13569
Gene ID 1080
Applications ELISA, IF, IP, WB
Working dilutions Optimal dilution should be determined by the end user.
The following are guidelines only :
ELISA (1:2000 - 1:32000)
WB (1:500 - 1:1000)
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