Fibrinogen goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IP |
Reactivities | Canine |
Fibrinogen goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IP |
Reactivities | Canine |
Mouse IgM (Fc specific) goat polyclonal antibody, TRITC
Applications | 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 1/80. |
Reactivities | Mouse |
Conjugation | TRITC |
Canine IgG (H+L chain) goat polyclonal antibody, FITC
Applications | Can be used to identify and measure IgG, antigen or antibody, 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; to identify a specific antigen or immune complex using a reference antibody of dog origin in the middle layer of the indirect 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. Working dilutions are usually between 1/20 and 1/120. |
Reactivities | Canine |
Conjugation | FITC |
Canine IgG (Fc specific) goat polyclonal antibody, FITC
Applications | Can be used in immunocytochemical and immunohistochemical staining of IgG at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating IgG antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of dog origin known to be of the IgG isotype in the middle layer of the indirect 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. Working dilutions are usually between 1/15 and 1/60, depending on the method used. |
Reactivities | Canine |
Conjugation | FITC |
Mouse IgM (Fc specific) goat polyclonal antibody, Biotin
Applications | Can be used in Immunocytochemical and Immunohistochemical staining of IgM at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating IgM antibodies in serodiagnostic microbiology and autoimmune diseases. To identify a specific antigen using a reference antibody of Mouse origin known to be of the IgM isotype in the middle layer of the indirect test procedure. In non-isotopic assay methodology (e.g. ELISA) to measure IgM in Mouse serum or other body fluids. As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. 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: For histochemical and Cytochemical use are usually between 1/100 and 1/250 In ELISA and comparable non-precipitating antibody-binding assays between 1/1500 and 1/6000. |
Reactivities | Mouse |
Conjugation | Biotin |
Mouse IgM (Fc specific) goat polyclonal antibody, FITC
Applications | 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. Working dilutions are usually between 1/20 and 1/80. |
Reactivities | Mouse |
Conjugation | FITC |
Canine IgM (Fc specific) goat polyclonal antibody, FITC
Applications | Can be used in Immunocytochemical and Immunohistochemical staining of IgM at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating IgM antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of dog origin known to be of the IgM isotype in the middle layer of the indirect 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. General Recommended Dilutions: are usually between 1/10 and 1/40, depending on the method used. |
Reactivities | Canine |
Conjugation | FITC |
Turkey IgG (H+L chain) goat polyclonal antibody, Biotin
Applications | Immunofluorescence. ELISA. Western blotting. Dot- and Slot-Immunoblotting. Immunohistochemistry. |
Reactivities | Turkey |
Conjugation | Biotin |
Turkey IgG (H+L chain) goat polyclonal antibody, Purified
Applications | Immunofluorescence. ELISA. Western blotting. Dot- and Slot-Immunoblotting. Immunohistochemistry. |
Reactivities | Turkey |
Conjugation | Unconjugated |
Turkey IgG (H+L chain) goat polyclonal antibody, PE
Applications | Immunofluorescence. ELISA. Western blotting. Dot- and Slot-Immunoblotting. Immunohistochemistry. |
Reactivities | Turkey |
Conjugation | PE |
Turkey IgG (H+L chain) goat polyclonal antibody, FITC
Applications | Immunofluorescence: < / = 1 µg/10e6 cells. ELISA. Western blotting. Dot- and Slot-Immunoblotting. Immunohistochemistry. |
Reactivities | Turkey |
Conjugation | FITC |
Mouse IgA (alpha chain specific) goat polyclonal antibody, PE
Applications | FLISA. Flow Cytometry. Immunofluorescence: ≤ 0.1 µg/106 cells. Immunohistochemistry. |
Reactivities | Mouse |
Conjugation | PE |
Mouse IgA (alpha chain specific) goat polyclonal antibody, Aff - Purified
Applications | Immunoblotting. Flow Cytometry. Immunohistochemistry. Enzyme-Linked-Immunosorbent-Assay (ELISA). Fluorescent-Linked-Immunosorbent-Assay (FLISA). |
Reactivities | Mouse |
Conjugation | Unconjugated |
Mouse IgA+IgG+IgM (H+L chain) goat polyclonal antibody, Aff - Purified
Applications | Indirect Immunostaining (In conjunction with mouse monoclonal antibodies). |
Reactivities | Mouse |
Conjugation | Unconjugated |
Chicken IgG / Chicken IgY (H+L chain) goat polyclonal antibody, Aff - Purified
Applications | ELISA: 1/10,000 dilutions produced a detectable signal, as measured using HRP-labeled Chicken anti-Goat IgG Antibody Cat.-No AP31796HR-N (1/5000 dilution). Western blot (1/5000). Immunocytochemistry. Immunohistochemistry (1/250). Immunoprecipitation (1/250). Immunoelectrophoresis: Chicken serum (3 µl) was placed in the center well (at the clear circle) and then subjected to electrophoresis. After electrophoresis was complete, goat anti-chicken serum (75 μl) was placed in the lower trough and A30-106-10 (75 μl) was placed in the upper trough. After overnight incubation at 4°C, the gel was washed, fixed and stained with Coomassie. Note the single precipitin line between the center well and upper trough. |
Reactivities | Chicken |
Conjugation | Unconjugated |