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Swine IgG (H&L) Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
Secondary Antibodies
F(ab')2 Chicken IgG (H&L) Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:3,000 IHC: 1:500 - 1:2,500 ELISA: 1:7,500 - 1:30,000 |
| Conjugation | HRP |
Monkey IgG (H&L) Antibody Biotin
| Applications | WB: 1:5,000 - 1:10,000 IHC: User Optimized ELISA: 1:50,000 - 1:100,000 |
| Conjugation | Unconjugated |
Fab Sheep IgG (H&L) Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
F(ab')2 Swine IgG (H&L) Antibody Peroxidase Conjugated
| Applications | WB: 1:2,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:100,000 |
| Conjugation | HRP |
Mouse IgM (H&L) Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Reactivities | Mouse |
| Conjugation | HRP |
Horse IgM mu chain Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
Chicken IgG (H&L) Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
Dog IgM mu chain Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
Dog IgG F(ab')2 Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
Goat IgG (H+L chain) rabbit polyclonal antibody, FITC
| Applications | Suitable for Immunofluorescence Microscopy and Flow Cytometry or FACS analysis as well as other antibody based fluorescent assays requiring lot-to-lot consistency. Recommended Dilutions: FLISA: 1/10,000-1/50,000. Flow Cytometry: 1/500-1/2,500. IF Microscopy: 1/1,000-1/5,000. |
| Reactivities | Goat |
| Conjugation | FITC |
Mouse IgM (Fc specific) rabbit polyclonal antibody, TRITC
| Applications | ELISA. Immunocytochemistry. (In)direct immunofluorescence Immunohistochemistry on Frozen Sections. Direct immunofluorescence staining of cytoplasmic Ig of appropriately treated cell and tissue substrates; to demonstrate immunoglobulins or specific antibodies in cells and tissues; to identify circulating antibodies in serodiagnostic microbiology and autoimmune diseases. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Working Dilutions: 1/10- 1/80. |
| Reactivities | Mouse |
| Conjugation | TRITC |
Mouse IgM (Fc specific) rabbit polyclonal antibody, FITC
| Applications | ELISA. Immunocytochemistry. Immunohistochemistry on Frozen Sections. (In)direct immunofluorescence. In direct staining of cytoplasmic IgM in fixed mouse cells and tissue substrates; to identify circulating IgM antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen or immune complex using a reference antibody of mouse in the middle layer of the test procedure. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Working Dilutions: 1/20- 1/80. |
| Reactivities | Mouse |
| Conjugation | FITC |
Mouse IgM (Fc specific) rabbit polyclonal antibody, Azide Free
| Applications | Can be used: As unlabelled primary or secondary antibody reagent for indirect detection of IgM in Mouse cells, tissues and body fluids in Immunofluorescence and Immunoenzyme assay methods. For the production of immunoconjugates with a selected marker. To prepare immunoaffinity adsorbents by coupling to an artificial carrier. In non-isotopic methodology based on solid phase immunochemistry (e.g. ELISA), both as catching antibody and detection reagent. In Western blotting. When applied in any immunocytochemical or histochemical staining procedure or solid phase coupling techniques, the optimum concentration of this product should be established before. Recommneded Working Dilutions: Histochemistry: 1/100-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/1000-1/5000. Precipitin titre: not less than 1/64 when tested against normal Mouse serum in agar-block immunodiffusion titration. Performance testing: Titre, specificity and reactivity of the subclass specific cross-adsorbed IgG is further evaluated in a number of highly sensitive non-precipitating antibody-binding assay systems. These performance tests include direct single and double identification of cIg in mouse cell and tissue substrates and their evaluation as second antibody in the analysis of human cells and tissues after reacting with a primary monoclonal mouse antibody to a human antigen. The quantitative specific recognition ability is verified in double staining procedures together with reference reagents of known specificity and reactivity. |
| Reactivities | Mouse |
| Conjugation | Unconjugated |
Duck IgG (H+L chain) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry on Paraffin Sections. In enzyme-immunocytochemical and immunohistochemical staining for the detection of duck IgG, antigen or antibody, of appropriately treated cell and tissue substrates at the cellular and subcellular level. In nonisotopic assay methodology (e.g. ELISA) to identify and measure a specific IgG in duck serum or other body fluid. In electron microscopy, since the complex between the conjugated antibody and the antigen also has electron-dense properties. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Working Dilutions: Histochemical and Cytochemical Use: 1/100-1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/5,000. |
| Reactivities | Duck |
| Conjugation | HRP |
