United States
Germany
Japan
United Kingdom
China
Rabbit anti-ACAT2 polyclonal antibody
| Applications | WB |
| Reactivities | Human, Rat, Sheep, Pig, Mouse |
Antibodies
Rabbit polyclonal anti CRF (ovine); neat antiserum
| Applications | ELISA |
| Reactivities | Sheep |
Rabbit Polyclonal Prion protein Antibody
| Applications | WB |
| Reactivities | Bovine, Sheep |
Rabbit Polyclonal Prion protein Antibody
| Applications | WB |
| Reactivities | Bovine, Sheep, Avian |
Rabbit Polyclonal Prion protein Antibody
| Applications | WB |
| Reactivities | Bovine, Sheep |
Rabbit polyclonal Hsp110 Antibody
| Applications | WB |
| Reactivities | Human, Monkey, Hamster, Rat, Mouse, Sheep, Yeast, Cow |
Rabbit polyclonal SOD (Mn) Antibody
| Applications | IHC |
| Reactivities | Human, Rat, Mouse, Bovine, Canine, Chicken, Gerbil, Guinea Pig, Pig, Hamster, Rabbit, Monkey, Sheep, Xenopus |
Rabbit Polyclonal Anti-Calnexin -CT Antibody
| Applications | WB |
| Reactivities | Human, Monkey, Mouse, Rat, Bovine, Dog, Hamster, Rabbit, Pig, Quail, Sheep, Xenopus (weak), Guinea Pig, Drosophila (weak), Chicken (weak) |
Goat Anti-C12orf29 (aa30-43) Antibody
| Applications | WB |
| Reactivities | Human (Expected from sequence similarity: Pig, Sheep, Cow) |
PTPH1 (PTPN3) pSer459 rabbit polyclonal antibody, Aff - Purified
| Applications | WB |
| Reactivities | Bovine, Canine, Human, Mouse, Primate, Sheep |
Sheep IgM (H+L chain) rabbit polyclonal antibody, Biotin
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry Paraffin Sections. Can be used in immunocytochemical and immunohistochemical staining for the detection of IgM 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, where IgM and IgG antibodies can be expected. 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: 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 | Biotin |
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 (H+L chain) rabbit polyclonal antibody, Biotin
| Applications | ELISA. Dot blot. Immunoblotting. Immunocytochemistry. Immunohistochemistry Paraffin Sections. 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 sheep 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: 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 | Biotin |
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 |
活动过滤器
优化搜索结果
Target Symbol
- CALNEXIN (3)
- COL2A1 (3)
- GFAP (3)
- PRION PROTEIN PRP (3)
- FSHB (2)
- H2A.Z (2)
- LUTEINIZING HORMONE BETA (2)
- PRL (2)
- SOD2 (2)
- ACAT2 (1)
- AQUAPORIN 2 (1)
- ARF5 (1)
- BETA ACTIN (1)
- C-MYC (1)
- C12ORF29 (1)
- CALRETICULIN (1)
- CAVEOLIN 2 (1)
- CHCHD3 (1)
- CHRM3 (1)
- CNPASE (1)
- COLLAGEN I (1)
- CPN10 (1)
- CRH (1)
- CRHR1 (1)
- CXCL8 (1)
- CXCR4 (1)
- DGAT1 (1)
- DOPA DECARBOXYLASE (1)
- EG5 (1)
- FABP2 (1)
- FBXL3 (1)
- FH (1)
- FOXO3 (1)
- GATA3 (1)
- GRP78 (1)
- HCRTR1 (1)
- HIF1 BETA (1)
- HSP105 (1)
- HSP40 (1)
- HSP70-1A (1)
- IDH1 (1)
- IGFBP6 (1)
- IL1B (1)
- IL6 (1)
- INHIBIN BETA A (1)
- ITGA6 (1)
- LACTOPEROXIDASE (1)
- MADH7 (1)
- MAPK3 (1)
- MUSCARINIC ACETYLCHOLINE RECEPTOR M3 (1)
- P38 (1)
- PDGF BETA (1)
- PERILIPIN-1 (1)
- PRNP (1)
- PROTEASOME SUBUNIT ALPHA TYPE 6 (1)
- PTPN3 (1)
- RHOC (1)
- ROR BETA (1)
- SMAD6 (1)
- SORD (1)
- SOX2 (1)
- SUPEROXIDE DISMUTASE 1 (1)
- TPX2 (1)
- TRH RECEPTOR (1)
- WNT2 (1)
Applications
Antibody Hosts
Assay Types
Families
- Druggable Genome (37)
- Transmembrane (12)
- ES Cell Differentiation/IPS (10)
- Transcription Factors (10)
- Stem cell - Pluripotency (8)
- Secreted Protein (7)
- Adult stem cells (3)
- Cancer stem cells (3)
- GPCR (3)
- Embryonic stem cells (2)
- Induced pluripotent stem cells (2)
- Stem cell relevant signaling - JAK/STAT signaling pathway (2)
- Stem cell relevant signaling - Wnt Signaling pathway (2)
- Nuclear Hormone Receptor (1)
- Protease (1)
- Protein Kinase (1)
- Stem cell relevant signaling - TGFb/BMP signaling pathway (1)
Pathways
- Antigen processing and presentation (6)
- Prion diseases (6)
- Pathways in cancer (5)
- Focal adhesion (4)
- MAPK signaling pathway (4)
- Metabolic pathways (4)
- Neuroactive ligand-receptor interaction (4)
- TGF-beta signaling pathway (4)
- Cytokine-cytokine receptor interaction (3)
- GnRH signaling pathway (3)
- Leukocyte transendothelial migration (3)
- Regulation of actin cytoskeleton (3)
- Renal cell carcinoma (3)
- Amyotrophic lateral sclerosis (ALS) (2)
- Calcium signaling pathway (2)
- Chemokine signaling pathway (2)
- Endocytosis (2)
- Endometrial cancer (2)
- Huntington's disease (2)
- Neurotrophin signaling pathway (2)
- Systemic lupus erythematosus (2)
- Tryptophan metabolism (2)
- Wnt signaling pathway (2)
- Acute myeloid leukemia (1)
- Adherens junction (1)
- Arrhythmogenic right ventricular cardiomyopathy (ARVC) (1)
- Axon guidance (1)
- Basal cell carcinoma (1)
- Bladder cancer (1)
- Butanoate metabolism (1)
- Cell cycle (1)
- Chronic myeloid leukemia (1)
- Citrate cycle (TCA cycle) (1)
- Colorectal cancer (1)
- Dilated cardiomyopathy (1)
- ECM-receptor interaction (1)
- Epithelial cell signaling in Helicobacter pylori infection (1)
- ErbB signaling pathway (1)
- Fatty acid metabolism (1)
- Fc epsilon RI signaling pathway (1)
- Gap junction (1)
- Glioma (1)
- Glycerolipid metabolism (1)
- Hedgehog signaling pathway (1)
- Histidine metabolism (1)
- Hypertrophic cardiomyopathy (HCM) (1)
- Jak-STAT signaling pathway (1)
- Lysine degradation (1)
- Melanogenesis (1)
- Melanoma (1)
- NOD-like receptor signaling pathway (1)
- Non-small cell lung cancer (1)
- PPAR signaling pathway (1)
- Pathogenic Escherichia coli infection (1)
- Phenylalanine metabolism (1)
- Progesterone-mediated oocyte maturation (1)
- Propanoate metabolism (1)
- Prostate cancer (1)
- Proteasome (1)
- Pyruvate metabolism (1)
- RIG-I-like receptor signaling pathway (1)
- Retinol metabolism (1)
- Small cell lung cancer (1)
- Spliceosome (1)
- Synthesis and degradation of ketone bodies (1)
- T cell receptor signaling pathway (1)
- Terpenoid backbone biosynthesis (1)
- Thyroid cancer (1)
- Tight junction (1)
- Toll-like receptor signaling pathway (1)
- Tyrosine metabolism (1)
- VEGF signaling pathway (1)
- Valine (1)
- Vibrio cholerae infection (1)
- Viral myocarditis (1)
- leucine and isoleucine degradation (1)
