Rabbit F(ab)2 anti-Cat IgG (H+L)-FITC, MinX none

Artikelnummer: DNA-SEC-183662
Artikelname: Rabbit F(ab)2 anti-Cat IgG (H+L)-FITC, MinX none
Artikelnummer: DNA-SEC-183662
Hersteller Artikelnummer: SEC-183662
Alternativnummer: DNA-SEC-183662
Hersteller: dianova
Wirt: Rabbit
Kategorie: Antikörper
Applikation: FLISA,FACS,IF
Spezies Reaktivität: Feline
Immunogen: Cat IgG whole molecule
Konjugation: FITC
Alternative Synonym: Rabbit F(ab)2 Anti-Cat fluorescein Conjugated Antibody, Rabbit Fab2 Anti-Cat Antibody fluorescein Conjugation, Rabbit Fab2 Anti-Cat Antibody FITC Conjugation
Format: F(ab')2
Spezifität: IgG (H+L)
Minimale Kreuzreaktivität (MinX): no cross-adsorbtion
F(ab)2 Antibody was generated by enzymatic cleavage and subsequent separation from the Fc fragment. Because of their smaller size, F(ab)2 fragments offer several advantages over intact antibodies for use in certain immunochemical techniques and experimen
Klonalität: Polyclonal
Konzentration: 1.0 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 Cat IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation.   Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Fluorescein, anti-Rabbit Serum, Cat IgG and Cat Serum.  No reaction was observed against anti-Pepsin or anti-Rabbit IgG F(c).  Limited reactivity will occur against Armenian Hamster IgG.
Formulierung: Lyophilized
Formel: 20 mM K3PO4,150 mM NaCl,pH 7,2,lyophilisate,0,01% NaN3
Target-Kategorie: Cat
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: 2.7, IF Microscopy Dilution: 1:1,000 - 1:5,000
Anwendungsbeschreibung: Suitable for immunomicroscopy and flow cytometry or FACS analysis as well as other antibody based fluorescent assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.