CNY 3940.00
5周
Antibodies
CNY 9630.00
5周
Human IgA (Secretory component) mouse monoclonal antibody, clone NI 194-4 (A89-039), HRP
| Applications | To identify the presence of free or bound Secretory component in Human serum, other body fluids, cell and tissue substrates and to determine its concentration in techniques as Radioimmunoassay, ELISA, Indirect Immunoperoxidase and Immunofluorescence staining, Haemagglutination and Immunoblotting. General Recommended Dilutions: Histochemical Use: from 1/20 upwards. ELISA: form 1/50 upwards. Western blot: from 1/100 upwards. |
| Reactivities | Human |
| Conjugation | HRP |
Goat Anti-Mouse IgG (H+L) HRP conjugated secondary antibody
| Applications | EIA and Western blots: 1:5,000-1:100,000. Immunohistochemistry: 1:500-1:5,000. Optimal working dilutions must be determined by end user. |
| Reactivities | Mouse |
| Conjugation | HRP |
Goat Anti-Rabbit IgG (H+L) HRP conjugated secondary antibody
| Applications | EIA and Western blots: 1:5,000-1:100,000. Immunohistochemistry: 1:500-1:5,000. Optimal working dilutions must be determined by end user. |
| Reactivities | Rabbit |
| Conjugation | HRP |
Goat Anti-Rabbit IgG (H+L) HRP conjugated secondary antibody
| Applications | EIA and Western blots: 1:5,000-1:100,000. Immunohistochemistry: 1:500-1:5,000. Optimal working dilutions must be determined by end user. |
| Reactivities | Rabbit |
| Conjugation | HRP |
Goat Anti-Mouse IgG (H+L) HRP conjugated secondary antibody
| Applications | EIA and Western blots: 1:5,000-1:100,000. Immunohistochemistry: 1:500-1:5,000. Optimal working dilutions must be determined by end user. |
| Reactivities | Mouse |
| Conjugation | HRP |
Mouse IgA (alpha chain specific) goat polyclonal antibody, HRP
| Applications | ELISA: 1/4,000-1/8,000. Immunoblotting. Immunohistochemistry. |
| Reactivities | Mouse |
| Conjugation | HRP |
Bovine IgG (H+L chain) goat polyclonal antibody, HRP
| Applications | Suitable for Immunoblotting (1/5,000-1/100,000, Western or dot blot), ELISA (1/10,000-1/200,000), Immunoperoxidase Electron Microscopy and Immunohistochemistry (1/500-1/5,000) as well as other peroxidase-antibody based enzymatic assays requiring lot-to-lot consistency. |
| Reactivities | Bovine |
| Conjugation | HRP |
Bovine IgG (Fc specific) rabbit polyclonal antibody, HRP
| Applications | Suitable for immunoblotting (western or dot blot 1:1,000 - 1:10,000), ELISA (1:10,000 - 1:50,000=, immunoperoxidase electron microscopy and immunohistochemistry (1:500 - 1;2,500) as well as other peroxidase-antibody based enzymatic assays requiring lot-to-lot consistency. This product has been assayed against 1.0 ug of Bovine IgG in a standard capture ELISA using ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at room temperature. A working dilution of 1:2,000 to 1:10,000 of the reconstitution concentration is suggested for this product. |
| Reactivities | Bovine |
| Conjugation | HRP |
Mouse IgG2a (gamma 2a chain specific) rabbit polyclonal antibody, HRP
| Applications | This secondary antibody anti-Mouse is ideal for investigators who routinely perform titration assays, Western-blot, Immunoprecipitation and more generally immunoassays. Anti-Mouse IgG2a heavy chain antibody is suitable for highly specific immunological methods requiring extremely low background levels, lot-to-lot consistency, high titer and specificity. Recommended Dilutions: ELISA: 1/90,000 Western blot: 1/2,000-1/10,000. Immunohistochemistry: 1/500-1/2,500. |
| Reactivities | Mouse |
| Conjugation | HRP |
Goat IgG (H+L chain) chicken polyclonal antibody, HRP
| Applications | ELISA: a 1/75,000 dilution gave an O.D. of 1.0 in a 15 minute reaction using Tetramethylbenzidine as substrate. Western Blot (1/5000). Quality Control: Antibodies were tested for specificity using Double-Immunodiffusion assays in Agarose gels and ELISA analysis. |
| Reactivities | Goat |
| Conjugation | HRP |
Canine IgE goat polyclonal antibody, HRP
| Applications | ELISA: 1/10,000-1/100,000. Western Blot: 1/1000-1/10,000. Immunohistochemistry on Frozen Sections: 1/200-1/500. |
| Reactivities | Canine |
| Conjugation | HRP |
Chicken IgA (Fc specific) goat polyclonal antibody, HRP
| Applications | In enzyme-immunocytochemical and immunohistochemical staining for the detection of IgA at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to demonstrate circulating IgA antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of chicken origin known to be of the IgA isotype in the middle layer of the indirect test procedure; in non-isotopic assay methodology (e.g. ELISA) to measure IgA in chicken serum or other body fluids. 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. Recommended Dilutions: ELISA and comparable non-precipitating antibody-binding assays: 1/500-1/5,000. Immunocytochemistry: 1/50-1/250. Immunohistochemistry: 1/50-1/250. |
| Reactivities | Chicken |
| Conjugation | HRP |
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 |
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