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

Produktübersicht

• Artikelname: Goat F(ab)2 anti-Horse IgG (H+L)-FITC, MinX none
• Artikelnummer: DNA-SEC-182681
• Hersteller Artikelnummer: SEC-182681
• Alternativnummer: DNA-SEC-182681
• Hersteller: dianova
• Wirt: Goat
• Kategorie: Antikörper
• Applikation: FLISA,FACS,IF
• Spezies Reaktivität: Equine
• Immunogen: Horse IgG whole molecule
• Konjugation: FITC
• Alternative Synonym: goat F(ab)2 anti-Horse IgG Antibody fluorescein Conjugated, goat F(ab)2 anti-Horse IgG FITC conjugated antibody
• Format: F(ab')2
• Spezifität: IgG (H+L)
• Minimale Kreuzreaktivität (MinX): no cross-adsorbtion

Produktbeschreibung

F(ab)2 Anti-Horse IgG Fluorescein 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 immunochemic

Produkteigenschaften

• Klonalität: Polyclonal
• Isotyp: Ig
• Puffer: 0.02 M Potassium 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, Horse IgG and Horse Serum. No reaction was observed against anti-Goat IgG F(c) or anti-Pepsin.
• Formulierung: Lyophilized
• Formel: 20 mM K3PO4,150 mM NaCl,pH 7,2,lyophilisate,Azide/BSA free
• Target-Kategorie: Horse
• Antibody Type: Secondary Antibody

Anwendungsbeschreibung

• Application Verdünnung: FLISA Dilution: 1:10,000 - 1:50,000, Flow Cytometry Dilution: 1:500 - 1:2,500, 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.

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