CFTR anticorps (N-Term)
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- Antigène Voir toutes CFTR Anticorps
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
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Épitope
- N-Term
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CFTR est non-conjugé
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Application
- Immunofluorescence (IF), Western Blotting (WB), ELISA, Immunoprecipitation (IP)
- Specificité
- Reacts with human CFTR
- Réactivité croisée
- Souris
- Réactivité croisée (Details)
- May cross-react with mouse CFTR due to sequence homology.
- Purification
- Antiserum
- Immunogène
- Synthetic peptide derived from Nter domain of human CFTR protein.
- Isotype
- IgG
- Top Product
- Discover our top product CFTR Anticorps primaire
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- Indications d'application
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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.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- 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.
- Date de péremption
- 24 months
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- Antigène
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
- Autre désignation
- Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) (CFTR Produits)
- Synonymes
- anticorps ABC35, anticorps ABCC7, anticorps CF, anticorps CFTR/MRP, anticorps MRP7, anticorps TNR-CFTR, anticorps dJ760C5.1, anticorps CFTR, anticorps AW495489, anticorps Abcc7, anticorps RGD1561193, anticorps abc35, anticorps abcc7, anticorps cftr/mrp, anticorps mrp7, anticorps tnr-cftr, anticorps xcftr, anticorps si:dkey-270i2.2, anticorps cystic fibrosis transmembrane conductance regulator, anticorps cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7), anticorps CFTR, anticorps cftr-A, anticorps Cftr, anticorps cftr
- Sujet
- Defects in CFTR are the cause of cystic fibrosis (CF) also known as mucoviscidosis.
- ID gène
- 1080
- UniProt
- P13569
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