CFTR Antikörper (N-Term)
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- Target Alle CFTR Antikörper anzeigen
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
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Bindungsspezifität
- N-Term
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser CFTR Antikörper ist unkonjugiert
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Applikation
- Immunofluorescence (IF), Western Blotting (WB), ELISA, Immunoprecipitation (IP)
- Spezifität
- Reacts with human CFTR
- Kreuzreaktivität
- Maus
- Kreuzreaktivität (Details)
- May cross-react with mouse CFTR due to sequence homology.
- Aufreinigung
- Antiserum
- Immunogen
- Synthetic peptide derived from Nter domain of human CFTR protein.
- Isotyp
- IgG
- Top Product
- Discover our top product CFTR Primärantikörper
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- Applikationshinweise
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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) - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Must be reconstituted in distilled water.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- 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.
- Haltbarkeit
- 24 months
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- Target
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
- Andere Bezeichnung
- Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) (CFTR Produkte)
- Synonyme
- ABC35 antikoerper, ABCC7 antikoerper, CF antikoerper, CFTR/MRP antikoerper, MRP7 antikoerper, TNR-CFTR antikoerper, dJ760C5.1 antikoerper, CFTR antikoerper, AW495489 antikoerper, Abcc7 antikoerper, RGD1561193 antikoerper, abc35 antikoerper, abcc7 antikoerper, cftr/mrp antikoerper, mrp7 antikoerper, tnr-cftr antikoerper, xcftr antikoerper, si:dkey-270i2.2 antikoerper, cystic fibrosis transmembrane conductance regulator antikoerper, cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) antikoerper, CFTR antikoerper, cftr-A antikoerper, Cftr antikoerper, cftr antikoerper
- Hintergrund
- Defects in CFTR are the cause of cystic fibrosis (CF) also known as mucoviscidosis.
- Gen-ID
- 1080
- UniProt
- P13569
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