Donkey F(ab)2 anti-Rat IgG (H+L)-HRPO, MinX Bo,Ck,Go,Gp,Hm,Ho,Hu,Ms,Rb,Sh, Polyclonal

Artikelnummer: DNA-SEC-183888
Artikelname: Donkey F(ab)2 anti-Rat IgG (H+L)-HRPO, MinX Bo,Ck,Go,Gp,Hm,Ho,Hu,Ms,Rb,Sh, Polyclonal
Artikelnummer: DNA-SEC-183888
Hersteller Artikelnummer: SEC-183888
Alternativnummer: DNA-SEC-183888
Hersteller: dianova
Wirt: Donkey
Kategorie: Antikörper
Applikation: ELISA,IHC,WB
Spezies Reaktivität: Rat
Immunogen: Rat IgG whole molecule
Konjugation: HRPO
Alternative Synonym: Donkey F(ab)2 Anti-Rat IgG Peroxidase Conjugated Antibody, Donkey F(ab)2 Anti-Rat IgG Antibody HRP Conjugation
Format: F(ab')2
Spezifität: IgG (H+L)
Minimale Kreuzreaktivität (MinX): Bovine,Gallus,Goat,Guinea pig,Hamster (all),Equine,Human,Mouse,Rabbit,Sheep
F(ab)2 Anti-Rat IgG (H&L) Antibody generated in donkey detects immunoglobulin g from Rat, both heavy and light chains of the antibody molecule are present. Each IgG has two antigen binding sites. Representing approximately 75% of serum immunoglobulins, I
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 Rat 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-Peroxidase, anti-Donkey Serum, Rat IgG and Rat Serum.  No reaction was observed against anti-Pepsin, anti-Donkey IgG F(c), or Bovine, Chicken, Goat, Guinea Pig, Hamster, Horse, Human, Mouse, Rabbit and Sheep serum proteins.
Formulierung: Lyophilized
Formel: 20 mM K3PO4,150 mM NaCl,pH 7,2,lyophilisate,0,01% Gentamicin
Target-Kategorie: Rat
Antibody Type: Secondary Antibody
Application Verdünnung: ELISA Dilution: 1:5,000 - 1:20,000, Immunohistochemistry Dilution: 1:500 - 1:2,000, Western Blot Dilution: 1:500 - 1:2,000
Anwendungsbeschreibung: Suitable for immunoblotting (western or dot blot), ELISA, immunoperoxidase electron microscopy and immunohistochemistry as well as other peroxidase-antibody based enzymatic assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity. Do not use sodium azide as a preservative.  Azide will substantially inhibit the enzyme activity of horseradish peroxidase.