Antibodies

Glycophorin A (GYPA) rabbit polyclonal antibody, FITC

Applications FC
Reactivities Human

Luciferase (Photinus pyralis) goat polyclonal antibody, FITC

Applications FC, IF

Human Lambda Light Chain goat polyclonal antibody, FITC

Applications FC, IF, IHC
Reactivities Human

Albumin rabbit polyclonal antibody, FITC

Applications ID, IF, IP, R
Reactivities Guinea Pig

C3 goat polyclonal antibody, FITC

Applications ID, IF, IHC, IP
Reactivities Rat

C3 goat polyclonal antibody, FITC

Applications ID, IF, IHC, IP
Reactivities Mouse

Fibrinogen goat polyclonal antibody, FITC

Applications ELISA, ID, IF, IP
Reactivities Canine

Monkey IgG (H+L chain) goat polyclonal antibody, FITC

Applications 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 monkey 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 1/80.
Reactivities Monkey
Conjugation FITC

Monkey IgA + IgG + IgM (H+L chain) goat polyclonal antibody, FITC

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; to identify a specific antigen or immune complex using a reference antibody of monkey 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 1/80.
Reactivities Monkey
Conjugation FITC

C3 goat polyclonal antibody, FITC

Applications ID, IF, IHC, IP
Reactivities Monkey

Human IgG (F(ab)2 specific) goat polyclonal antibody, FITC

Applications Direct staining of fixed cell and tissue substrates, to demonstrate the intracellular presence of free of Ig
bound subunits of both kappa and lambda type. The absence of the Fc domain in the conjugate ensures minimal interaction with the tissue components and cell surfaces other than the primary antibody activity.
This conjugate is primarily intended for use in cell surface membrane staining procedures, to identify and quantitate Ig on B cells, especially if interference by Fc activity is expected.
Recommended Dilutions: 1/20-1/80.
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.
Reactivities Human
Conjugation FITC

Borrelia burgdorferi rabbit polyclonal antibody, FITC, Purified

Applications IF
Reactivities Bacteria

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 IgG (adsorbed) goat polyclonal antibody, FITC

Applications Flow Cytometry: Use 50 µl of 1/50-1/200 diluted antibody to label 1x106 cells in 100 µl.
Reactivities Mouse
Conjugation FITC

Canine IgA (Fc specific) goat polyclonal antibody, FITC

Applications Can be used in immunocytochemical and immunohistochemical staining of IgA at the cellular and subcellular level 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 dog origin known to be of the IgA isotype in the middle layer of the indirect test procedure. 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 1/20 and 1/80, depending on the method used.
Reactivities Canine
Conjugation FITC