IL12A goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Canine, Human, Porcine, Monkey |
IL12A goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Canine, Human, Porcine, Monkey |
Monkey IgG (H+L chain) goat polyclonal antibody, Azide Free
Applications | 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: In histochemistry are usually between 1/50 and 1/250. In ELISA and comparable non-precipitating antibody-binding assays between 1/500 and 1/5000. |
Reactivities | Monkey |
Conjugation | Unconjugated |
Monkey IgG (Fc specific) goat polyclonal antibody, TRITC
Applications | Can be used for 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. Working dilutions are usually between 1/10 and 1/30. |
Reactivities | Monkey |
Conjugation | TRITC |
Monkey IgM (Fc specific) goat polyclonal antibody, TRITC
Applications | Can be used for direct immunofluorescence staining of cytoplasmic IgM 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. Working dilutions are usually between 1/10 and 1/40. |
Reactivities | Monkey |
Conjugation | TRITC |
Monkey IgA + IgG + IgM (H+L chain) goat polyclonal antibody, TRITC
Applications | Can be used for 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. Working dilutions are usually between 1/10 and 1/40. |
Reactivities | Monkey |
Conjugation | TRITC |
Monkey IgA (Fc specific) goat polyclonal antibody, TRITC
Applications | Can be used for 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. Antisera to IgA do not discriminate between serum IgA (monomeric and dimeric) and higher molecular forms such as secretory IgA. 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. Working dilutions are usually between 1/10 and 1/30. |
Reactivities | Monkey |
Conjugation | TRITC |
Axin 1 (AXIN1) (850-862) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Human, Mouse, Rat, Canine, Bovine, Bat, Equine, Hamster, Monkey, Zebrafish |
Human IgE goat polyclonal antibody, AP
Applications | ELISA: 1/1000-1/10000. Western Blot: 1/1000-1/5000. |
Reactivities | Human, Monkey |
Conjugation | AP |
Human IgE goat polyclonal antibody, FITC
Applications | Flow Cytometry. |
Reactivities | Human, Monkey |
Conjugation | FITC |
Goat Polyclonal Anti-REP1 Antibody
Applications | WB |
Reactivities | Canine, Human, Monkey, Mouse, Rat |
Monkey IgM (Fc specific) goat polyclonal antibody, Azide Free
Applications | 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: In Histochemistry are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays between 1/500 and 1/5000. |
Reactivities | Monkey |
Conjugation | Unconjugated |
Monkey IgA (Fc specific) goat polyclonal antibody, Azide Free
Applications | 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. Antisera to IgA do not discriminate between serum IgA (monomeric and dimeric) and higher molecular forms such as secretory IgA. 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: In histochemistry are usually between 1/50 and 1/250. In ELISA and comparable non-precipitating antibody-binding assays between 1/500 and 1/2500. |
Reactivities | Monkey |
Conjugation | Unconjugated |
Monkey IgA + IgG + IgM (Fc specific) goat polyclonal antibody, Azide Free
Applications | The cytochemical grade allows the use in different types of highly sensitive immunoassays on appropriately treated cell and tissue substrates; in radioimmunoassay; 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. This product is not pre-diluted. The optimum working dilution of each product should be established by titration before being used. Working dilutions: For histochemical and cytochemical use are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays are between 1/1000 and 1/5000. |
Reactivities | Monkey |
Conjugation | Unconjugated |
Monkey IgA + IgG + IgM (H+L chain) goat polyclonal antibody, Azide Free
Applications | This IgG fraction allows the use in different types of highly sensitive immunoassays on appropriately treated cell and tissue substrates; in radioimmunoassay; 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. This product is not pre-diluted. The optimum working dilution of each product should be established by titration before being used. Working dilutions: For histochemical and cytochemical use are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays are between 1/1000 and 1/5000. |
Reactivities | Monkey |
Conjugation | Unconjugated |
C3 goat polyclonal antibody, Azide Free
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Monkey |