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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
Defects in CFTR are the cause of cystic fibrosis (CF) also known as mucoviscidosis.

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Price From: €165.00
Ref : 00014058

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Product Code pab0716-P
Immunogen Synthetic peptide derived from Nter domain of human CFTR protein.
Target Specificity Reacts with human CFTR. May cross-react with mouse CFTR due to sequence homology.
Name Cystic fibrosis transmembrane conductance regulator (CFTR)
Uniprot ID P13569
Gene ID 1080
Print datasheet
Product type Primary antibodies
Clonality Polyclonal antibody
Produced in Rabbit
Species Human
Labelling None
Appearance Lyophilized powder
Conc. / Activity 1 mg/ml
Form Purified (protein A)
Constituents Tris 0,1M, glycine 0,1M, sucrose 2%
Preservatives None
Recommendations Must be reconstituted in distilled water to reach 1 mg/ml.
Storage 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.
Applications Western Blot, Immunofluorescence, ELISA, Immunoprecipitation
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)
Research areas Cell biology,Disease-related biomarkers
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IF - CFTR antibody<br/>(pab0716-P)<br/>Anti-CFTR antibody IF staining of BHK cells expressing wild-type (wt) or mutated CFTR (rDF508).

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