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| Catalog Number | orb1878754 |
|---|---|
| Category | Antibodies |
| Description | The Goat Mouse/Rabbit IgG (H&L)-HRP Polymer (Ready to use) Antibody is suitable for ELISA, ICC, IHC, WB. It is a Polyclonal, HRP conjugated antibody which raised against Mouse/Rabbit IgG. Purification: Goat Polyclonal Secondary Antibody to Mouse/Rabbit IgG (H&L) have been cross-adsorbed against IgG from bovine, goat, horse and human. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in less background staining and cross-reactivity. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. Further passages through additional columns result in highly cross-adsorbed preparations of secondary antibody. The benefits of these extra steps are apparent in multiplexing/multicolor-staining experiments where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there may be the presence of endogenous immunoglobulins. |
| Clonality | Polyclonal |
| Species/Host | Goat |
| Conjugation | HRP |
| Reactivity | Mouse, Rabbit |
| Form/Appearance | Liquid in PBS, pH 7.2, containing 1% rAlbumin, 0.05% Proclin |
| Purification | Goat Polyclonal Secondary Antibody to Mouse/Rabbit IgG (H&L) have been cross-adsorbed against IgG from bovine, goat, horse and human. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in less background staining and cross-reactivity. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. Further passages through additional columns result in highly cross-adsorbed preparations of secondary antibody. The benefits of these extra steps are apparent in multiplexing/multicolor-staining experiments where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there may be the presence of endogenous immunoglobulins. |
| Immunogen | Mouse/Rabbit IgG |
| Tested applications | ELISA, ICC, IHC, WB |
| Dilution range | Ready to use |
| Antibody Type | Secondary Antibody |
| Storage | Shipped and store at 4°C for one year. |
| Note | For research use only |
| Expiration Date | 12 months from date of receipt. |

Immunohistochemical analysis staining in human liver carcinoma formalin fixed paraffin-embedded tissue section. The section was pre-treated using pressure cooker heat antigen retrieval with sodium citrate buffer (0.01 M, pH = 6) for 3 minutes. The section was detected using mouse primary antibody, and Goat Anti-Mouse/Rabbit IgG (H&L)-HRP polymer (Ready to use). The section was then counterstained with haematoxylin and mounted with Neutral Gum.

Immunohistochemical analysis staining in human liver carcinoma formalin fixed paraffin-embedded tissue section. The section was pre-treated using pressure cooker heat antigen retrieval with sodium citrate buffer (0.01 M, pH = 6) for 3 minutes. The section was detected using rabbit primary antibody, and Goat Anti-Mouse/Rabbit IgG (H&L)-HRP polymer (Ready to use). The section was then counterstained with haematoxylin and mounted with Neutral Gum.
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