CFTR antibody (N-Term)

Catalog No. ABIN559718

The Rabbit Polyclonal anti-CFTR antibody (ABIN559718) specifically detects CFTR in IF, WB, ELISA and IP. The antibody is reactive with Human samples.

Quick Overview for CFTR antibody (N-Term) (ABIN559718)

Target: CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CFTR antibody is un-conjugated

Application: Immunofluorescence (IF), Western Blotting (WB), ELISA, Immunoprecipitation (IP)

Product Details anti-CFTR Antibody

Binding Specificity: N-Term

Specificity: Reacts with human CFTR

Cross-Reactivity: Mouse (Murine)

Cross-Reactivity (Details): May cross-react with mouse CFTR due to sequence homology.

Purification: Antiserum

Immunogen: Synthetic peptide derived from Nter domain of human CFTR protein.

Isotype: IgG

Application Details

Application Notes:

Working dilution: Optimal dilution should be determined by the end user.
The following are guidelines only :
ELISA(1:2000 - 1:32000) WB(1:500 - 1:1000)

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Must be reconstituted in distilled water.

Storage: 4 °C/-20 °C

Storage Comment: 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.

Expiry Date: 24 months

Target Details for CFTR

Target: CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))

Alternative Name: Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

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

Gene ID: 1080

UniProt: P13569