Rabbit Fab anti-Sheep IgG (H+L)-FITC, MinX none

Artikelnummer: DNA-SEC-183981
Artikelname: Rabbit Fab anti-Sheep IgG (H+L)-FITC, MinX none
Artikelnummer: DNA-SEC-183981
Hersteller Artikelnummer: SEC-183981
Alternativnummer: DNA-SEC-183981
Hersteller: dianova
Wirt: Rabbit
Kategorie: Antikörper
Applikation: FLISA,FACS,IF
Spezies Reaktivität: Sheep
Immunogen: Sheep IgG whole molecule
Konjugation: FITC
Alternative Synonym: Rabbit Fab Anti-Sheep IgG Antibody Fluorescein Conjugation, Rabbit Fab Anti-Sheep IgG FITC Conjugated Antibody
Format: Fab
Spezifität: IgG (H+L)
Minimale Kreuzreaktivität (MinX): no cross-adsorbtion
Fab Anti-Sheep IgG (H&L) Antibody generated in rabbit detects sheep IgG. Representing approximately 75% of serum immunoglobulins, IgG is the most abundant antibody isotype found in the circulation. IgG molecules are synthesized and secreted by plasma B c
Klonalität: Polyclonal
Konzentration: 0.5 mg/mL
Isotyp: Ig
Puffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Reinheit: This product was prepared from monospecific antiserum by immunoaffinity chromatography using Sheep IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, papain digestion and chromatographic separation.   Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Fluorescein and anti-Rabbit Serum.  No reaction was observed against anti-Papain or anti-Rabbit IgG F(c).
Formulierung: Lyophilized
Formel: 20 mM K3PO4,150 mM NaCl,pH 7,2,lyophilisate,0,01% NaN3
Target-Kategorie: Sheep
Antibody Type: Secondary Antibody
Application Verdünnung: FLISA Dilution: 1:10,000 - 1:50,000, Flow Cytometry Dilution: 1:500 - 1:2,500, Fluorochrome Protein Value: 1.2, IF Microscopy Dilution: 1:1,000 - 1:5,000
Anwendungsbeschreibung: This product is designed for immunofluorescence microscopy, fluorescence based plate assays (FLISA) and fluorescent western blotting. This product is also suitable for multiplex analysis, including multicolor imaging, utilizing various commercial platforms requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.