Human IgE goat polyclonal antibody, FITC
Applications | Flow Cytometry. |
Reactivities | Human, Monkey |
Conjugation | FITC |
Human IgE goat polyclonal antibody, FITC
Applications | Flow Cytometry. |
Reactivities | Human, Monkey |
Conjugation | FITC |
CLEC2D (122-131) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Human, Equine, Monkey |
KMT2B (2703-2715) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Human, Mouse, Rat, Bovine, Monkey, Porcine, Zebrafish |
PCK1 (513-524) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Canine, Human, Mouse, Rat, Bat, Equine, Monkey, Rabbit |
MTLRP (GHRL) (103-117) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Hamster, Human, Monkey, Mouse, Porcine, Rat |
RELM beta (RETNLB) (Internal) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Human, Monkey |
DAP12 (TYROBP) (Internal) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Human, Bat, Canine, Equine, Monkey |
GNAT3 / Gustducin Goat Polyclonal (Internal) Antibody
Applications | IHC |
Reactivities | Bovine, Dog, Gorilla, Human, Monkey, Mouse, Pig, Rabbit, Rat, Gibbon, Hamster, Horse (Predicted: Bat) |
SNX12 (150-162) goat polyclonal antibody, Aff - Purified
Applications | ELISA, IHC |
Reactivities | Human, Mouse, Bovine, Bat, Hamster, Monkey, Porcine, Rabbit |
Monkey IgM (Fc specific) goat polyclonal antibody, Azide Free
Applications | As unlabelled primary or secondary reagent for indirect detection techniques, to prepare conjugates with markers 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 or detection antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical procedure or solids phase coupling technique, the optimum concentration of the IgG preparation should always be established by titration. Recommended Working Dilutions: In Histochemistry are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays between 1/500 and 1/5000. |
Reactivities | Monkey |
Conjugation | Unconjugated |
Monkey IgG (H+L chain) goat polyclonal antibody, Azide Free
Applications | As unlabelled primary or secondary reagent for indirect detection techniques, to prepare conjugates with markers 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 or detection antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical procedure or solids phase coupling technique, the optimum concentration of the IgG preparation should always be established by titration. Recommended 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 | Monkey |
Conjugation | Unconjugated |
Monkey IgG (Fc specific) goat polyclonal antibody, TRITC
Applications | Can be used for 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 1/30. |
Reactivities | Monkey |
Conjugation | TRITC |
Monkey IgM (Fc specific) goat polyclonal antibody, TRITC
Applications | Can be used for direct immunofluorescence staining of cytoplasmic IgM 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 1/40. |
Reactivities | Monkey |
Conjugation | TRITC |
Monkey IgA (Fc specific) goat polyclonal antibody, Azide Free
Applications | Can be used as unlabelled primary or secondary reagent for indirect detection techniques, to prepare conjugates with markers 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 or detection antibody in non-isotopic methodology and solid phase immunochemistry. Antisera to IgA do not discriminate between serum IgA (monomeric and dimeric) and higher molecular forms such as secretory IgA. When applied in any cytochemical or histochemical procedure or solids phase coupling technique, the optimum concentration of the IgG preparation should always be established by titration. Recommended 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 1/2500. |
Reactivities | Monkey |
Conjugation | Unconjugated |
Monkey IgA + IgG + IgM (H+L chain) goat polyclonal antibody, TRITC
Applications | Can be used for 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 1/40. |
Reactivities | Monkey |
Conjugation | TRITC |