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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
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
Ref
00014058
Defects in CFTR are the cause of cystic fibrosis (CF) also known as mucoviscidosis.
| 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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