Alb goat polyclonal antibody, FITC
Applications | ELISA, IF, IHC, IP, R |
Reactivities | Rat |
Alb goat polyclonal antibody, FITC
Applications | ELISA, IF, IHC, IP, R |
Reactivities | Rat |
Alb goat polyclonal antibody, Azide Free
Applications | ELISA, ID, IF, IP, WB |
Reactivities | Rat |
Mouse IgM (Fc specific) goat polyclonal antibody, Azide Free
Applications | Can be used as unlabelled primary or secondary reagent for indirect detection of IgM at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to prepare conjugates 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 antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical staining procedure or solid phase coupling technique, the optimum concentration of the IgG preparation should be established by titration before being used. Typical 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 | Mouse |
Conjugation | Unconjugated |
Properdin (CFP) goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Human |
Bovine Serum Proteins goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Bovine |
Lactoferrin (LTF) goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Human |
C3 goat polyclonal antibody, HRP
Applications | ELISA, ID, IF, IP, WB |
Reactivities | Guinea Pig |
Human Kappa Light Chain (free and bound) goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Human |
Mouse Kappa Light Chain (free and bound) goat polyclonal antibody, HRP
Applications | ELISA, ID, IF, IHC, WB |
Reactivities | Mouse |
Human Lambda Light Chain (free and bound) goat polyclonal antibody, TRITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Human |
Fibrinogen goat polyclonal antibody, HRP
Applications | ELISA, ID, IF, IHC, WB |
Reactivities | Mouse |
Complement C3 (C3) goat polyclonal antibody, TRITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Human |
Mouse Serum Proteins goat polyclonal antibody, FITC
Applications | ELISA, ID, IF, IHC, IP |
Reactivities | Mouse |
Porcine IgM (Fc specific) goat polyclonal antibody, Biotin
Applications | Can be used: • In immunocytochemical and immunohistochemical use for the detection of IgM at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates. • To demonstrate circulating IgM antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using an reference antibody of goat 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 swine 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. Recommended Working Dilutions: Histochemical and Cytochemical Use: 1/100-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/1000-1/5000. |
Reactivities | Porcine |
Conjugation | Biotin |
Porcine IgM (Fc specific) goat polyclonal antibody, HRP
Applications | Can be used: • In enzyme-immunocytochemical and immunohistochemical staining for the detection of IgM at the cellular and subcellular level by staining 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 swine 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 swine serum or other body fluids. 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: 1/50-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/1000-1/5000. |
Reactivities | Porcine |
Conjugation | HRP |