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Fibrinogen goat polyclonal antibody, Biotin
| Applications | ELISA, ID, IF, IHC, IP, WB |
| Reactivities | Mouse |
Products
Monkey IgG (H+L chain) goat polyclonal antibody, Biotin
| Applications | Can be used in immunocytochemical and immunohistochemical staining to identify and measure IgG, antigen or antibody, at the cellular and subcellular level by 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. 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: For histochemical and cytochemical use are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays between 1/1000 and 1/5000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgM (Fc specific) goat polyclonal antibody, Biotin
| Applications | Can be used in immunocytochemical and immunohistochemical staining of IgM at the cellular and subcellular level 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 monkey 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 monkey 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 are usually between 1/100 and 1/250. ELISA and comparable non-precipitating antibody-binding assays between 1/1000 and 1/3000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgA (Fc specific) goat polyclonal antibody, Biotin
| 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 monkey 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 monkey serum or other body fluids. As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. 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: For histochemical and cytochemical use are usually between 1/100 and 1/250. In ELISA and comparable non-precipitating antibody-binding assays between 1/1000 and 1/4000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgA + IgG + IgM (Fc specific) goat polyclonal antibody, Biotin
| Applications | Can be used in immunocytochemical and immunohistochemical staining of immunoglobulins at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of monkey origin in the middle layer of the indirect test procedure; in non-isotopic assay methodology (e.g. ELISA) to measure immunoglobulins in monkey serum or other body fluids. The absence of activity to the common Ig/Fab subunit prevents the reaction of this conjugate with immunoglobulins bounds to Fc receptors on non-lymphoid cells. 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. Working dilutions: For histochemical and cytochemical use are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays between 1/2000 and 1/10000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgG (Fc specific) goat polyclonal antibody, Biotin
| Applications | This antibody can be used in Immunocytochemical and Immunohistochemical staining of IgG at the cellular and subcellular level of appropriately treated cell and tissue substrates. To demonstrate circulating IgG antibodies in serodiagnostic microbiology and autoimmune diseases, To identify a specific antigen using a reference antibody of monkey origin known to be of the IgG isotype in the middle layer of the indirect test procedure, in non-isotopic assay methodology (e.g. ELISA) to measure IgG in Monkey 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. Working Dilutions Histochemical and Cytochemical Use: 1/100-1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/5000-1/20000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgA + IgG + IgM (H+L chain) goat polyclonal antibody, Biotin
| Applications | Can be used in immunocytochemical and immunohistochemical staining of immunoglobulins at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of monkey origin in the middle layer of the indirect test procedure; in non-isotopic assay methodology (e.g. ELISA) to measure immunoglobulins in monkey 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. Working dilutions: For histochemical and cytochemical use are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays between 1/2000 and 1/10000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Mouse IgG3 (subclass specific) goat polyclonal antibody, Biotin
| Applications | Can be used in Immunocytochemical and Immunohistochemical staining for the detection of IgG3 at the cellular and subcellular level 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. 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. Working dilutions Histochemical and Cytochemical: 1/100 - 1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/1.000 - 1/5,000. |
| Reactivities | Mouse |
| Conjugation | Biotin |
Rat IgE (Fc specific) goat polyclonal antibody, Biotin
| Applications | This antibody can be used In Immunocytochemical and Immunohistochemical staining for the detection of IgE at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology. In non-isotopic assay methodology (e.g. ELISA) to identify and measure IgE in rat serum or other body fluid. As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Dilutions: Histochemistry and Cytochemistry: 1/100-1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/10,000. |
| Reactivities | Rat |
| Conjugation | Biotin |
Rabbit 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 rabbit 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: 1/100 - 1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/1000 - 1/10000. |
| Reactivities | Rabbit |
| Conjugation | Biotin |
Human IgD (Fc specific) goat polyclonal antibody, Biotin
| Applications | Can be used in Immunocytochemical and Immunohistochemical staining for the detection of IgD at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology. In non-isotopic assay methodology (e.g. ELISA) to identify and measure IgD in human serum or other body fluid. 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 Dilutions: Histochemical and Cytochemical Use: 1/100-1/250 ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/10,000. Performance testing. Isotype specificity and quantitative specific recognition ability are further evaluated at the high level of sensitivity by direct singe and simultaneous double staining of different types of human cells, using counterstaining with reference conjugates with a different marker. The immunoconjugate is further tested in ELISA-type assays. |
| Reactivities | Human |
| Conjugation | Biotin |
Guinea Pig IgG2 (subclass specific) goat polyclonal antibody, Biotin
| Applications | In immunocytochemical and immunohistochemical staining for the detection of IgG2 at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating IgG2 antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of guinea pig origin known to be of the IgG2 isotype in the middle layer of the indirect test procedure; in non-isotopic assay methodology (e.g. ELISA) to measure IgG2 in guinea pig 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. Working dilutions: Histochemical and Cytochemical: 1/50 - 1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/200 - 1/2000. |
| Reactivities | Guinea Pig |
| Conjugation | Biotin |
Rabbit IgA (Fc specific) goat polyclonal antibody, Biotin
| Applications | 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 rabbit 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 rabbit serum or other body fluids. As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. 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 working dilutions: Histochemical and Cytochemical: 1/50 - 1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/100 - 1/1000. |
| Reactivities | Rabbit |
| Conjugation | Biotin |
Alb goat polyclonal antibody, Biotin
| Applications | ELISA, IF, IHC, IP, R, WB |
| Reactivities | Rat |
Canine IgG (H+L chain) goat polyclonal antibody, Biotin
| Applications | Can be used in immunocytochemical and immunohistochemical staining to identify and measure IgG, antigen or antibody, at the cellular and subcellular level by 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 dog origin in the middle layer of the indirect test procedure. 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. Working dilutions: For histochemical and cytochemical use are usually between 1/100 and 1/500. In ELISA and comparable non-precipitating antibody-binding assays between 1/1000 and 1/10000. |
| Reactivities | Canine |
| Conjugation | Biotin |
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Target Symbol
- C3 (4)
- CCL7 (4)
- IL12A (4)
- RETN (4)
- CCL15 (3)
- CCL24 (3)
- IL3 (3)
- ACHE (2)
- ADIPOQ (2)
- AIMP1 (2)
- ALB (2)
- ALDOA (2)
- ALPHA DEFENSIN 1 (2)
- CCL13 (2)
- CCL16 (2)
- CCL3L1 (2)
- CD40LG (2)
- CXCL12 (2)
- CXCL16 (2)
- DEFB4A (2)
- EGF (2)
- FGF10 (2)
- FGF16 (2)
- FGF17 (2)
- FOLR1 (2)
- GDHB (2)
- GLNA (2)
- GLPK (2)
- GPD1 (2)
- IFNG (2)
- IGF1 (2)
- IL12A , IL12B (2)
- IL17 (2)
- IL18BP (2)
- IL1A (2)
- IL2 (2)
- IL20 (2)
- IL6 (2)
- LACTOFERRIN (2)
- LDHA (2)
- LEP (2)
- MSTN (2)
- PFKM (2)
- PGMB (2)
- PKM (2)
- PPBP (2)
- PROK1 (2)
- SCGF (2)
- SDF1 (2)
- SOXA (2)
- THPO (2)
- TNF (2)
- TNFRSF13B (2)
- TNFRSF9 (2)
- TNFSF11 (2)
- TNFSF12 (2)
- TNFSF13B (2)
- VEGFA (2)
- YCJM (2)
- ZWF (2)
- ABC3735 (1)
- ACP3 (1)
- ALDH5A1 (1)
- ALDH9A1 (1)
- AMPK ALPHA 2 (1)
- AMYA (1)
- BLRO_MYRVE (1)
- C22ORF28 (1)
- CA1 (1)
- CCL11 (1)
- CHOA (1)
- CHOX_ALCSP (1)
- CLIP170 (1)
- CMG1 (1)
- COMPLEMENT C3 (1)
- DCUN1D1 (1)
- EWSR1 (1)
- FGA (1)
- GAG CAPSID PROTEIN P24 (1)
- GFP (1)
- GNB3 (1)
- GP120 (1)
- GRIA4 (1)
- IL1B (1)
- INV1 (1)
- LAF (1)
- MATRIX PROTEIN M1 (1)
- MOMP (1)
- NAM-DH (1)
- NONO (1)
- O+K ANTIGENS (1)
- P2OX (1)
- PCNA (1)
- PGA (1)
- PGA5 (1)
- PKC BETA 1 (1)
- PPI (1)
- RPEB (1)
- SDF4 (1)
- SEPTIN6 (1)
Reactivities
- Human (108)
- Mouse (46)
- Rabbit (25)
- Rat (21)
- Monkey (12)
- Escherichia coli (6)
- Chicken (5)
- Guinea Pig (5)
- Porcine (5)
- Canine (4)
- Hamster (4)
- Bacillus species (3)
- Influenza A Virus (3)
- Bacteria (2)
- Bacterial (2)
- Bovine (2)
- Brevibacterium (2)
- Carica papaya (2)
- Ferret (2)
- Human Immunodeficiency Virus 1 (2)
- Lactococcus lacti (2)
- Leuconostoc mesenteroides (2)
- Rhizopus (2)
- A. victoria (1)
- Alcaligenes (1)
- Bacillus sp. (1)
- Candida (1)
- Candida species (1)
- Chlamydia trachomatis (1)
- Corynebacterium diphtheriae (1)
- Duck (1)
- Hepatitis B Virus (1)
- Influenza B Virus (1)
- Microbial (1)
- Mouse IgG (1)
- Myrothecium (1)
- Myrothecium verrucaria (1)
- Nebraska Calf Diarrhoea Virus (1)
- Respiratory Syncytial Virus (1)
- Schistosoma japonicum (1)
- Streptomyces (1)
- Turkey (1)
Clonalities
Assay Types
Families
Pathways
- Cytokine-cytokine receptor interaction (8)
- Chemokine signaling pathway (4)
- Jak-STAT signaling pathway (4)
- Toll-like receptor signaling pathway (4)
- Hypertrophic cardiomyopathy (HCM) (3)
- Leukocyte transendothelial migration (3)
- Pathways in cancer (3)
- Allograft rejection (2)
- Axon guidance (2)
- Butanoate metabolism (2)
- Cytosolic DNA-sensing pathway (2)
- Graft-versus-host disease (2)
- Hematopoietic cell lineage (2)
- Metabolic pathways (2)
- NOD-like receptor signaling pathway (2)
- Prion diseases (2)
- RIG-I-like receptor signaling pathway (2)
- Type I diabetes mellitus (2)
- Adipocytokine signaling pathway (1)
- Alanine (1)
- Arginine and proline metabolism (1)
- Ascorbate and aldarate metabolism (1)
- B cell receptor signaling pathway (1)
- Base excision repair (1)
- Calcium signaling pathway (1)
- Cell cycle (1)
- Complement and coagulation cascades (1)
- DNA replication (1)
- ErbB signaling pathway (1)
- Fatty acid metabolism (1)
- Fc epsilon RI signaling pathway (1)
- Fc gamma R-mediated phagocytosis (1)
- Focal adhesion (1)
- Gap junction (1)
- Glioma (1)
- Glycerolipid metabolism (1)
- Glycolysis / Gluconeogenesis (1)
- GnRH signaling pathway (1)
- Histidine metabolism (1)
- Insulin signaling pathway (1)
- Limonene and pinene degradation (1)
- Long-term depression (1)
- Long-term potentiation (1)
- Lysine degradation (1)
- MAPK signaling pathway (1)
- Melanogenesis (1)
- Mismatch repair (1)
- Natural killer cell mediated cytotoxicity (1)
- Neuroactive ligand-receptor interaction (1)
- Non-small cell lung cancer (1)
- Nucleotide excision repair (1)
- Phosphatidylinositol signaling system (1)
- Propanoate metabolism (1)
- Pyruvate metabolism (1)
- Regulation of autophagy (1)
- Systemic lupus erythematosus (1)
- Taste transduction (1)
- Tight junction (1)
- Tryptophan metabolism (1)
- VEGF signaling pathway (1)
- Valine (1)
- Vascular smooth muscle contraction (1)
- Vibrio cholerae infection (1)
- Wnt signaling pathway (1)
- aspartate and glutamate metabolism (1)
- beta-Alanine metabolism (1)
- leucine and isoleucine degradation (1)
- mTOR signaling pathway (1)
