HOXD8 mouse monoclonal antibody,clone OTI1E3, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse |
HOXD8 mouse monoclonal antibody,clone OTI1E3, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse |
ITM2A mouse monoclonal antibody,clone OTI8C3, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse, Rat |
ITM2A mouse monoclonal antibody,clone OTI10C11, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse, Rat |
CNY 3,990.00
2周
IPO5 mouse monoclonal antibody,clone OTI1C5, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse, Rat |
CNY 3,990.00
2周
IPO5 mouse monoclonal antibody,clone OTI3B8, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse, Rat |
CNY 3,990.00
2周
IPO5 mouse monoclonal antibody,clone OTI4C3, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse, Rat |
RFC3 mouse monoclonal antibody,clone OTI2E5, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse, Rat |
KLF7 mouse monoclonal antibody,clone OTI7G1, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse |
KLF7 mouse monoclonal antibody,clone OTI8D7, HRP conjugated
Applications | WB |
Reactivities | Human, Mouse |
Mouse IgG (H+L chain), adsorbed donkey polyclonal antibody, HRP
Applications | Suitable for Immunoblotting (1/2,000-1/20,000 for Western blot), ELISA (1/180,000), Immunoperoxidase electron microscopy and Immunohistochemistry (1/1,000-1/5,000) as well as other peroxidase-antibody based enzymatic assays requiring lot-to-lot consistency. Recommended Dilutions: This product has been assayed against 1.0 µg of Mouse 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 1/20,000 to 1/80,000 of the reconstitution concentration is suggested for this product. |
Reactivities | Mouse |
Conjugation | HRP |
C3 goat polyclonal antibody, HRP
Applications | ELISA, ID, IF, IHC, IP, WB |
Reactivities | Mouse |
Mouse IgM (Fc specific) rabbit polyclonal antibody, HRP
Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry on Paraffin Sections. 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 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. 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- 1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000- 1/5,000. |
Reactivities | Mouse |
Conjugation | HRP |
Mouse 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 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. 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 1/400. In ELISA and comparable non-precipitating antibody-binding assays between 1/1000 and 1/8000 depending on the method used. |
Reactivities | Mouse |
Conjugation | HRP |
Mouse IgG3 (subclass specific) goat polyclonal antibody, HRP
Applications | This antibody can be used in Enzyme-Immunocytochemical and Immunohistochemical staining for the detection of IgG3 at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates To demonstrate circulating IgG3 antibodies in serodiagnostic microbiology and autoimmune diseases. To identify a specific antigen using a reference antibody of mouse origin known to be of the IgG3 isotype in the middle layer of the indirect test procedure In non-isotopic assay methodology (e.g. ELISA) to measure IgG3 in Mouse 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. Working Dilutions: Histochemical/Cytochemical Use: 1/100-1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/7,000 depending on the method used. Working dilutions schould be stored at +4°C, not refrozen, and preferably used the same day. |
Reactivities | Mouse |
Conjugation | HRP |
Mouse IgE (Fc specific) rabbit polyclonal antibody, HRP
Applications | Can be used in enzyme-immunocytochemical and immunohistochemical staining for the detection of IgE at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to demonstrate circulating IgE antibodies in mouse serum or other body fluids; in non-isotopic assay methodology (e.g. ELISA) to identify and measure IgE in mouse 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: 1/100 - 1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/500 - 1/5000. |
Reactivities | Mouse |
Conjugation | HRP |