You have no items in your shopping cart.
You have no items in your shopping cart.
Catalog Number | orb346626 |
---|---|
Category | Antibodies |
Description | Horse IgG F(ab')2 antibody |
Species/Host | Goat |
Clonality | Polyclonal |
Tested applications | ELISA, IHC, WB |
Reactivity | Equine |
Isotype | IgG |
Immunogen | Horse IgG F(ab')2 fragment |
Concentration | 10.0 mg/mL |
Dilution range | ELISA: 1:20,000 - 1:100,000, IHC: 1:1,000 - 1:5,000, WB: 1:2,000 - 1:10,000 |
Form/Appearance | Lyophilized |
Purity | This product is an IgG fraction antibody purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum, Horse IgG, Horse IgG F(ab’)2 and Horse Serum. No reaction was observed against Horse IgG F(c). |
Conjugation | Unconjugated |
Storage | Store vial at 4° C prior to restoration. For extended storage aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use. |
Buffer/Preservatives | 0.01% (w/v) Sodium Azide |
Alternative names | goat anti-Horse IgG F(ab')2 fragment Antibody, goa Read more... |
Note | For research use only |
Application notes | Anti-Horse IgG F(ab')2 antibody is suitable for ELISA, western blot, and immunohistochemistry, as well as other assays requiring lot-to-lot consistency. |
Expiration Date | 12 months from date of receipt. |
IP | |
Agarose | |
This product is a purified Horse IgG isolated from normal Horse Serum digested by the enzyme pepsin and purified by chromatography coupled to activated agarose. Sufficient antibody capacity is provided to bind a minimum of 5.0 mg of anti-Horse IgG. | |
Horse |
SDS-PAGE | |
Unconjugated | |
This product was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by pepsin digestion and extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Horse IgG, anti-Horse IgG F(ab’)2 and anti-Horse Serum. No reaction was observed against anti-Horse IgG F(c) or anti-Pepsin. | |
Horse |
FITC | |
This product was prepared from normal serum by delipidation, salt fractionation and ion change chromatography followed by pepsin digestion and extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Fluorescein, anti-Horse IgG, anti-Horse IgG F(ab’)2 and anti-Horse Serum. No reaction was observed against anti-Horse IgG F(c) or anti-Pepsin. | |
Horse |
HRP | |
This product was prepared from normal serum by delipidation, salt fractionation, ion exchange chromatography followed by pepsin digestion and extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Peroxidase, anti-Horse IgG, anti-Horse IgG F(ab’)2 and anti-Horse Serum. No reaction was observed against anti-Horse IgG F(c) or anti-Pepsin. | |
Horse |
Biotin | |
This product was prepared from normal serum delipidation, salt fractionation, ion exchange chromatography followed by pepsin digestion and extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-biotin, anti-Horse IgG, anti-Horse IgG F(ab’)2 and anti-Horse Serum. No reaction was observed against anti-Horse IgG F(c) or anti-Pepsin. | |
Horse |
Filter by Rating