Products
Monkey IgG (H+L chain) rabbit polyclonal antibody, HRP
| Applications | In enzyme-immunocytochemical and immunohistochemical staining for the detection of IgG, antigen or antibody, of appropriately treated cell and tissue substrates at the cellular and subcellular level. In non-isotopic assay methodology (e.g. ELISA) to identify and measure a specific IgG in monkey serum or other body fluid. In electron microscopy, since the complex between the conjugated antibody and the antigen also has electron-dense properties. 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: 1/1,000-1/8,000. |
| Reactivities | Monkey |
| Conjugation | HRP |
Monkey IgG (H+L chain) rabbit 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. Working dilutions: Histochemical and cytochemical: 1/100 - 1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/2000 - 1/10000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgA + IgG + IgM (H+L chain) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry on Paraffin Sections. Can be used in Enzyme-Immunocytochemical and Immunohistochemical staining for the detection of IgG, antigen or antibody, of appropriately treated cell and tissue substrates at the cellular and subcellular level. In non-isotopic assay methodology (e.g. ELISA) to identify and measure a specific IgG in monkey serum or other body fluid. In electron microscopy, since the complex between the conjugated antibody and the antigen also has electron-dense properties. 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: 1/2000-1/8000. |
| Reactivities | Monkey |
| Conjugation | HRP |
Monkey IgA + IgG + IgM (H+L chain) rabbit polyclonal antibody, Biotin
| Applications | Can be usde 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. Recommended working dilutions: Histochemical and cytochemical: 1/100 - 1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/2000 - 1/20000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Monkey IgA + IgG + IgM (H+L chain) rabbit polyclonal antibody, FITC
| 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; 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 IgG (Fab specific) rabbit polyclonal antibody, Biotin
| Applications | In immunocytochemical and immunohistochemical staining to identify and measure free or Ig bound subunits of both kappa and lambda type 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. In general this kind of products is not recommended as direct or indirect screening reagents for immunoglobulin isotypes on the surface of membranes of vital lymphoid cells. The presence of activity to the common Fab subunit may result in the staining of Ig bound to Fc-receptors on non-lymphoid cells. Combinations of isotype-specific reagents should be used instead for this purpose. 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: 1/1,000-1/10,000. |
| Reactivities | Monkey |
| Conjugation | Biotin |
Porimin (TMEM123) (173-188) rabbit polyclonal antibody, Purified
| Applications | IHC, WB |
| Reactivities | Human, Bovine, Chicken, Mouse, Rat, Monkey, Rabbit |
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- ANXA5 (4)
- GAPDH (4)
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- ALPHA 1B ADRENERGIC RECEPTOR (2)
- ATP5F1B (2)
- CALNEXIN (2)
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- CCNA1 (2)
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- CD147 (1)
- CD16 (1)
- CD22 (1)
- CD247 (1)
- CD274 (1)
Applications
Conjugates
Modifications
- Unmodified (10)
- Phospho-specific (2)
- This chimeric rabbit antibody was made using the variable domain sequences of the original Mouse IgG1 format for improved compatibility with existing reagents assays and techniques. (2)
- This chimeric rabbit antibody was made using the variable domain sequences of the original Human IgG1 format for improved compatibility with existing reagents assays and techniques. (1)
- This chimeric rabbit antibody was made using the variable domain sequences of the original Human IgG4 format for improved compatibility with existing reagents assays and techniques. (1)
Isotypes
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Families
- Druggable Genome (142)
- Transmembrane (95)
- GPCR (25)
- Transcription Factors (20)
- Secreted Protein (18)
- Stem cell - Pluripotency (15)
- ES Cell Differentiation/IPS (14)
- Protease (12)
- Protein Kinase (7)
- Cancer stem cells (5)
- Ion Channels: Potassium (5)
- Adult stem cells (3)
- Embryonic stem cells (3)
- Induced pluripotent stem cells (3)
- Nuclear Hormone Receptor (3)
- Ion Channels: ATP Receptors (2)
- Ion Channels: Other (2)
- Ion Channels: Transient receptor potential (2)
- P450 (2)
- Phosphatase (1)
- Stem cell relevant signaling - DSL/Notch pathway (1)
- Stem cell relevant signaling - Wnt Signaling pathway (1)
Pathways
- Metabolic pathways (26)
- Pathways in cancer (22)
- Neuroactive ligand-receptor interaction (21)
- MAPK signaling pathway (16)
- Wnt signaling pathway (15)
- Basal cell carcinoma (13)
- Calcium signaling pathway (12)
- Hedgehog signaling pathway (11)
- Amyotrophic lateral sclerosis (ALS) (10)
- Huntington's disease (10)
- Melanogenesis (10)
- Antigen processing and presentation (9)
- Cell cycle (9)
- Progesterone-mediated oocyte maturation (8)
- Prostate cancer (8)
- Purine metabolism (8)
- Apoptosis (7)
- Colorectal cancer (7)
- Vascular smooth muscle contraction (7)
- p53 signaling pathway (7)
- Alzheimer's disease (6)
- Androgen and estrogen metabolism (6)
- Chemokine signaling pathway (6)
- Endocytosis (6)
- Glycolysis / Gluconeogenesis (6)
- Neurotrophin signaling pathway (6)
- Parkinson's disease (6)
- VEGF signaling pathway (6)
- Chronic myeloid leukemia (5)
- Fc epsilon RI signaling pathway (5)
- Glioma (5)
- Natural killer cell mediated cytotoxicity (5)
- Non-small cell lung cancer (5)
- Pancreatic cancer (5)
- Toll-like receptor signaling pathway (5)
- Cell adhesion molecules (CAMs) (4)
- Cytokine-cytokine receptor interaction (4)
- Endometrial cancer (4)
- Epithelial cell signaling in Helicobacter pylori infection (4)
- Fc gamma R-mediated phagocytosis (4)
- Leukocyte transendothelial migration (4)
- Melanoma (4)
- Prion diseases (4)
- Regulation of actin cytoskeleton (4)
- Small cell lung cancer (4)
- Spliceosome (4)
- Tight junction (4)
- Adipocytokine signaling pathway (3)
- Arachidonic acid metabolism (3)
- B cell receptor signaling pathway (3)
- Bladder cancer (3)
- C21-Steroid hormone metabolism (3)
- Focal adhesion (3)
- Glutathione metabolism (3)
- GnRH signaling pathway (3)
- Jak-STAT signaling pathway (3)
- NOD-like receptor signaling pathway (3)
- PPAR signaling pathway (3)
- Renal cell carcinoma (3)
- T cell receptor signaling pathway (3)
- Thyroid cancer (3)
- Ubiquitin mediated proteolysis (3)
- Viral myocarditis (3)
- Citrate cycle (TCA cycle) (2)
- DNA replication (2)
- ErbB signaling pathway (2)
- Gap junction (2)
- Long-term depression (2)
- Lysosome (2)
- Nicotinate and nicotinamide metabolism (2)
- Notch signaling pathway (2)
- Oocyte meiosis (2)
- Pantothenate and CoA biosynthesis (2)
- Pathogenic Escherichia coli infection (2)
- RNA degradation (2)
- Riboflavin metabolism (2)
- Starch and sucrose metabolism (2)
- mTOR signaling pathway (2)
- ABC transporters (1)
- Acute myeloid leukemia (1)
- Adherens junction (1)
- Amino sugar and nucleotide sugar metabolism (1)
- Arginine and proline metabolism (1)
- Axon guidance (1)
- Basal transcription factors (1)
- Base excision repair (1)
- Caffeine metabolism (1)
- Complement and coagulation cascades (1)
- Cysteine and methionine metabolism (1)
- Drug metabolism - other enzymes (1)
- ECM-receptor interaction (1)
- Ether lipid metabolism (1)
- Fructose and mannose metabolism (1)
- Glycerolipid metabolism (1)
- Glycerophospholipid metabolism (1)
- Hematopoietic cell lineage (1)
- Insulin signaling pathway (1)
- Linoleic acid metabolism (1)
- Long-term potentiation (1)
- Metabolism of xenobiotics by cytochrome P450 (1)
- Mismatch repair (1)
- N-Glycan biosynthesis (1)
- Nucleotide excision repair (1)
- Olfactory transduction (1)
- One carbon pool by folate (1)
- Phosphatidylinositol signaling system (1)
- Pyrimidine metabolism (1)
- Pyruvate metabolism (1)
- RIG-I-like receptor signaling pathway (1)
- Ribosome (1)
- Selenoamino acid metabolism (1)
- Sphingolipid metabolism (1)
- Type I diabetes mellitus (1)
- Type II diabetes mellitus (1)
- Vibrio cholerae infection (1)
- alpha-Linolenic acid metabolism (1)
