CFTR antibody (N-Term)
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- Target See all CFTR Antibodies
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
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Binding Specificity
- N-Term
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CFTR antibody is un-conjugated
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Application
- Immunofluorescence (IF), Western Blotting (WB), ELISA, Immunoprecipitation (IP)
- 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
- Top Product
- Discover our top product CFTR Primary Antibody
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- Application Notes
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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
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- 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
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- Target
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
- Alternative Name
- Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) (CFTR Products)
- Synonyms
- ABC35 antibody, ABCC7 antibody, CF antibody, CFTR/MRP antibody, MRP7 antibody, TNR-CFTR antibody, dJ760C5.1 antibody, CFTR antibody, AW495489 antibody, Abcc7 antibody, RGD1561193 antibody, abc35 antibody, abcc7 antibody, cftr/mrp antibody, mrp7 antibody, tnr-cftr antibody, xcftr antibody, si:dkey-270i2.2 antibody, cystic fibrosis transmembrane conductance regulator antibody, cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) antibody, CFTR antibody, cftr-A antibody, Cftr antibody, cftr antibody
- Background
- Defects in CFTR are the cause of cystic fibrosis (CF) also known as mucoviscidosis.
- Gene ID
- 1080
- UniProt
- P13569
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