Dog IgM mu chain Antibody Peroxidase Conjugated
| Applications | WB: 1:1,000 - 1:10,000 IHC: 1:500 - 1:2,500 ELISA: 1:10,000 - 1:50,000 |
| Conjugation | HRP |
Antibodies
Dextranase Antibody Peroxidase Conjugated
| Applications | ELISA, IP, WB |
| Reactivities | Penicillium |
Annexin V Rabbit polyclonal Antibody (HRP)
| Applications | WB |
| Reactivities | Human, Monkey |
Annexin V Rabbit polyclonal Antibody (HRP)
| Applications | WB |
| Reactivities | Human, Monkey |
FITC rabbit polyclonal antibody, HRP
| Applications | ELISA, WB |
ADH1 rabbit polyclonal antibody, HRP, Purified
| Applications | ELISA, IHC, IP, WB |
| Reactivities | Yeast |
Acetylated Lysine rabbit polyclonal antibody, HRP, Aff - Purified
| Applications | ELISA, IF, IP, WB |
alpha Lactalbumin (LALBA) rabbit polyclonal antibody, HRP
| Applications | ELISA, IF, IHC, WB |
| Reactivities | Human |
Porcine IgG (H+L chain) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry 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 swine serum or other body fluid. In electron microscopy, since the complex between the conjugated antibody and the antigen also has electrondense 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: Histochemistry and Cytochemical Use: 1/100-1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/10,000. |
| Reactivities | Porcine |
| Conjugation | HRP |
Sheep IgM (Fc specific) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry Paraffin Sections. 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 sheep 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 sheep 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: Histochemistry and Cytochemical Use: 1/50-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/500-1/5,000. |
| Reactivities | Sheep |
| Conjugation | HRP |
Sheep IgM (H+L chain) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry Paraffin Sections. 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, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases, where IgM and IgG antibodies can be expected. 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: Histochemistry and Cytochemical Use: 1/100-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/2,000-1/10,000. |
| Reactivities | Sheep |
| Conjugation | HRP |
Sheep IgG (H+L chain) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry 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 sheep 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: Histochemistry and Cytochemical Use: 1/100-1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/10.000. |
| Reactivities | Sheep |
| Conjugation | HRP |
Sheep IgG (Fc specific) 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 at the cellular and subcellular level by staining 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 sheep 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 sheep 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: Histochemistry and Cytochemical Use: 1/100-1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/8.000. |
| Reactivities | Sheep |
| Conjugation | HRP |
Duck IgG (H+L chain) rabbit polyclonal antibody, HRP
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry on Paraffin Sections. In enzyme-immunocytochemical and immunohistochemical staining for the detection of duck IgG, antigen or antibody, of appropriately treated cell and tissue substrates at the cellular and subcellular level. In nonisotopic assay methodology (e.g. ELISA) to identify and measure a specific IgG in duck 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: 1/1,000-1/5,000. |
| Reactivities | Duck |
| Conjugation | HRP |
LYZ rabbit polyclonal antibody, HRP
| Applications | ELISA, IF, IHC, WB |
| Reactivities | Human |
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Target Symbol
- KTI3 (4)
- ALB (3)
- AVD (3)
- CA2 (3)
- LACZ (3)
- LYZ (3)
- AAO (2)
- ADA (2)
- ADH1 (2)
- ALD2 (2)
- ANSB (2)
- ANXA5 (2)
- ARG1 (2)
- B2M (2)
- CAS9 (2)
- CAT (2)
- CELA1 (2)
- CPA1 (2)
- CPB1 (2)
- DEX (2)
- DLD LAD (2)
- GALM (2)
- GLUD1 (2)
- GOX (2)
- MAPK1 (2)
- PAP3 (2)
- PHOA (2)
- PRC1 (2)
- RNASE1 (2)
- SOD1 (2)
- TF (2)
- XDH (2)
- ALP1 (1)
- ALPHA-AMYLASE (1)
- ALPI (1)
- AMPC (1)
- BMY1 (1)
- BMY1, AMYB (1)
- C-MYC (1)
- CCL27 (1)
- CES1 (1)
- CES3 (1)
- COL2A1 (1)
- COL3A1 (1)
- COL5A1-COL5A3 (1)
- DNASE1 (1)
- DNASE1, DNL1 (1)
- FTH1 (1)
- GFP (1)
- HIS (1)
- HXK1 (1)
- HXK2 (1)
- INFECTED CELL PROTEIN (1)
- LALBA (1)
- O+H ANTIGENS (1)
- O+K ANTIGENS (1)
- ORM1 (1)
- PAP1 (1)
- PEP1 (1)
- PEPC (1)
- PKC DELTA (1)
- PRSS2 (1)
- SEROGROUP 4 (1)
- SERPINB14 (1)
- SURFACE ANTIGEN (1)
- TRBOTR (1)
- UREA_CANEN (1)
- VR1 (1)
Reactivities
- Human (30)
- Mouse (24)
- Porcine (15)
- Rat (15)
- Bovine (14)
- Sheep (12)
- Goat (10)
- Escherichia coli (6)
- Chicken (5)
- Monkey (5)
- Horse (4)
- Feline (3)
- Guinea Pig (3)
- Streptomyces avidinii (3)
- Yeast (3)
- Bacillus amyloliquefacies (2)
- Dog (2)
- Hamster (2)
- Legionella pneumophila (2)
- Penicillium (2)
- Pig (2)
- A. victoria (1)
- Aspergillus (1)
- Aspergillus niger (1)
- Borrelia burgdorferi (1)
- Canavalia ensiformis (Jack Bean) (1)
- Candida (1)
- Chlamydia trachomatis (1)
- Cucurbita (1)
- Donkey (1)
- Duck (1)
- Enterobacter (1)
- Enterobacter cloacae (1)
- Golden Syrian Hamster (1)
- Helicobacter pylori (1)
- Hepatitis B Virus (1)
- Human Alphaherpesvirus 1 (1)
- Human Alphaherpesvirus 2 (1)
- Jack Bean (1)
- Lima Bean (1)
- Listeria monocytogenes (1)
- Maize (1)
- Mycobacterium tuberculosis (1)
- Neisseria gonorrhoeae (1)
- Pigeon (1)
- Rabbit (1)
- Salmonella species (1)
- Soy Bean (1)
- Streptococcus (1)
- Streptococcus sp. (1)
- Sweet Potato (1)
- Treponema pallidum (1)
Isotypes
Clonalities
Assay Types
Families
- Druggable Genome (4)
- Embryonic stem cells (1)
- Induced pluripotent stem cells (1)
- Ion Channels: Transient receptor potential (1)
- Protein Kinase (1)
- Stem cell - Pluripotency (1)
- Stem cell relevant signaling - JAK/STAT signaling pathway (1)
- Stem cell relevant signaling - TGFb/BMP signaling pathway (1)
- Stem cell relevant signaling - Wnt Signaling pathway (1)
- Transcription Factors (1)
- Transmembrane (1)
Pathways
- Chemokine signaling pathway (2)
- Acute myeloid leukemia (1)
- Bladder cancer (1)
- Cell cycle (1)
- Chronic myeloid leukemia (1)
- Colorectal cancer (1)
- Cytokine-cytokine receptor interaction (1)
- Endometrial cancer (1)
- ErbB signaling pathway (1)
- Fc epsilon RI signaling pathway (1)
- Fc gamma R-mediated phagocytosis (1)
- GnRH signaling pathway (1)
- Jak-STAT signaling pathway (1)
- MAPK signaling pathway (1)
- Neuroactive ligand-receptor interaction (1)
- Neurotrophin signaling pathway (1)
- Pathways in cancer (1)
- Small cell lung cancer (1)
- TGF-beta signaling pathway (1)
- Thyroid cancer (1)
- Tight junction (1)
- Type II diabetes mellitus (1)
- Vascular smooth muscle contraction (1)
- Wnt signaling pathway (1)
