Goat F(ab)2 anti-Rat IgG (H+L)-FITC, MinX none

Artikelnummer: DNA-SEC-182705
Artikelname: Goat F(ab)2 anti-Rat IgG (H+L)-FITC, MinX none
Artikelnummer: DNA-SEC-182705
Hersteller Artikelnummer: SEC-182705
Alternativnummer: DNA-SEC-182705
Hersteller: dianova
Wirt: Goat
Kategorie: Antikörper
Applikation: FLISA,FACS,IF
Spezies Reaktivität: Rat
Immunogen: Rat IgG whole molecule
Konjugation: FITC
Alternative Synonym: goat F(ab)2 Anti-Rat IgG fluorescein conjugated Antibody, goat F(ab)2 Anti-Rat IgG FITC conjugated Antibody, goat Fab2 Anti-Rat IgG antibody fluorescein conjugation
Format: F(ab')2
Spezifität: IgG (H+L)
Minimale Kreuzreaktivität (MinX): no cross-adsorbtion
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 platfor
Klonalität: Polyclonal
Konzentration: 10.0 mg/mL
Isotyp: Ig
Puffer: 0.01 M Sodium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Reinheit: This product is a F(ab’)2  fragment of an IgG fraction antibody purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation, ion exchange chromatography and pepsin digestion followed by extensive dialysis against the buffer stated above.  Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-fluorescein, anti-Goat Serum, Rat IgG and Rat Serum.  No reaction was observed against anti-Goat IgG F(c) or anti-Pepsin.
Formulierung: Lyophilized
Formel: 10 mM NaPO4,150 mM NaCl,pH 7,2,lyophilisate,0,01% Thimerosal
Target-Kategorie: Rat
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: 3.5, 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.