You have no items in your shopping cart.
You have no items in your shopping cart.
Catalog Number | orb1289520 |
---|---|
Category | Proteins |
Description | Horse IgG protein |
Tested applications | IH, IP, WB |
Form/Appearance | Purified Horse IgG in PBS, pH 7.3, 0.01% sodium azide. |
Purity | Greater than 95% as determined by reducing SDS-PAGE. |
Source | Horse |
Storage | Store it at -20°C to -80°C for one year. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
Buffer/Preservatives | Purified Horse IgG in PBS, pH 7.3, 0.01% sodium azide. |
Note | For research use only |
Application notes | Please minimize freeze-thaw cycles. |
Expiration Date | 6 months from date of receipt. |
ELISA, IHC, SDS-PAGE, WB | |
Unconjugated | |
Horse IgG whole molecule was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and extensive dialysis against the buffer stated above. Horse IgG whole molecule was assayed by immunoelectrophoresis resulted in a single precipitin arc against anti-Horse IgG, and anti-Horse Serum. | |
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 |
SDS-PAGE | |
Unconjugated | |
Horse IgG whole molecule was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and extensive dialysis against the buffer stated above. Horse IgG whole molecule was assayed by immunoelectrophoresis resulted in a single precipitin arc against anti-Horse IgG, and anti-Horse Serum. | |
Horse |
SDS-PAGE | |
Unconjugated | |
Horse IgG F(c) fragment was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation, ion exchange chromatography and papain digestion followed by chromatographic separation and extensive dialysis against the buffer stated above. Horse IgG F(c) fragment assayed by immunoelectrophoresis resulted in a single precipitin arc against anti-Horse Serum, anti-Horse IgG and anti-Horse IgG F(c). No reaction was observed against anti-Horse IgG F(ab’)2 or anti-Papain. | |
Horse |
ELISA, IHC, WB | |
Equine | |
Rabbit | |
Polyclonal | |
HRP |