Bovine 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 |
Bovine 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 |
Bovine IgG F(ab')2 Antibody
Applications | WB: 1:2,000 - 1:10,000 IHC: 1:1,000 - 1:5,000 ELISA: 1:20,000 - 1:100,000 |
Conjugation | Unconjugated |
Bovine IgM mu chain Antibody
Applications | WB: 1:2,000 - 1:10,000 IHC: 1:1,000 - 1:5,000 ELISA: 1:20,000 - 1:100,000 |
Conjugation | Unconjugated |
Bovine 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 |
Bovine 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 |
Bovine IgG (H&L) Antibody
Applications | WB: 1:2,000 - 1:10,000 IHC: 1:1,000 - 1:5,000 ELISA: 1:20,000 - 1:100,000 |
Conjugation | Unconjugated |
Mouse IgG (H+L chain) rabbit polyclonal antibody, Ig Fraction
Applications | Immunoprecipitation. Immunodiffusion. Ouchterlony Test: Sample size: 15 µl. Distance between wells: 5 mm. Test Time: 5 days. Temperature: 37°C. Samples Tested: Normal mouse Serum (NMS), Purified mouse IgG, Normal human serum (NHS), Purified human IgG. Results: Specificity: a single band against NMS was detected at dilutions of 1/4 and 1/8 which is homogeneous with band to purified mouse IgG. No bands were detected against human IgG at 5 mg/ml or NHS at 1/4 dilution. Protein content: Biuret Assay 14 mg/ml. |
Reactivities | Mouse |
Conjugation | Unconjugated |
Human IgG rabbit polyclonal antibody, Ig Fraction
Applications | Immunoprecipitation. Immunodiffusion. |
Reactivities | Human |
Conjugation | Unconjugated |
Rat IgG2c rabbit polyclonal antibody, Purified
Applications | ELISA: 1µg/ml - 10µg/ml. Western Blot. Flow Cytometry. |
Reactivities | Human, Rat |
Conjugation | Unconjugated |
Rat IgG2b rabbit polyclonal antibody, Purified
Applications | ELISA: 1µg/ml - 10µg/ml. Western Blot. Flow Cytometry. |
Reactivities | Rat |
Conjugation | Unconjugated |
Sheep IgM (H+L chain) rabbit polyclonal antibody, Azide Free
Applications | ELISA. Dot blot. Immunoblotting. Indirect Immunofluorescence. Can be used as unlabelled primary or secondary reagent for indirect detection techniques, to prepare conjugates with markers of the user’s own choice, to prepare an insoluble immunoaffinity adsorbent or a solid phase antibody reagent by coupling to an artificial carrier and as catching or detection antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical procedure or solids phase coupling technique, the optimum concentration of the IgG preparation should always be established by titration. Recommended Working Dilutions: Histochemistry Use: 1/50-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/500-1/5,000. Precipitin titre: 1/64 when tested against pooled normal sheep serum in agar-block immunodiffusion titration. |
Reactivities | Sheep |
Conjugation | Unconjugated |
Sheep IgM (H+L chain) rabbit polyclonal antibody, FITC
Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry Frozen Sections. Can be used to identify IgM at the cellular and subcellular level by immunofluorescence staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases, where IgM and IgG antibodies can be expected. 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 | Sheep |
Conjugation | FITC |
Sheep IgG (H+L chain) rabbit polyclonal antibody, Azide Free
Applications | ELISA. Dot blot. Immunoblotting. Indirect Immunofluorescence. Can be used as unlabelled primary or secondary reagent for indirect detection techniques, to prepare conjugates with markers of the user’s own choice, to prepare an insoluble immunoaffinity adsorbent or a solid phase antibody reagent by coupling to an artificial carrier and as catching or detection antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical procedure or solids phase coupling technique, the optimum concentration of the IgG preparation should always be established by titration. Recommended Working Dilutions: Histochemistry Use: 1/50-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/500-1/5.000. Precipitin titre: 1/64 when tested against pooled normal sheep serum in agar-block immunodiffusion titration. |
Reactivities | Sheep |
Conjugation | Unconjugated |
Goat IgG (H&L) Antibody Peroxidase Conjugated Pre-Adsorbed
Reactivities | Goat |
Conjugation | HRP |
F(ab')2 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 |