WB
Various whole cell lysates were separated by 4-8% SDS-PAGE, and the membrane was blotted with anti-CD206/MRC1 antibody. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody. Lane 1: Mouse liverWB
Western blot analysis of lysates from MUTZ-3 WT and knockdown cell. Cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with CD206/MRC1 PT0527R PT Rabbit mAb. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.IHC
Human colon was stained with anti-CD206/MRC1 rabbit antibody| Product Name | CD206/MRC1 Rabbit mAb |
|---|---|
| Antibody Type | Primary Antibodies |
| Immunogen | Synthesized peptide derived from human N-ternal CD206 |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | IHCWB |
| WB:1:5000-1:20000 IHC:1:200-1:1000 |
|
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Purification | Affinity purified |
| Gene Symbol | MRC1 |
|---|---|
| Gene Synonyms | MMR hMR CD206 MRC1L1 CLEC13D CLEC13DL bA541I19.1 |
| Gene Full Name | mannose receptor C-type 1 |
| Gene Summary | The recognition of complex carbohydrate structures on glycoproteins is an important part of several biological processes, including cell-cell recognition, serum glycoprotein turnover, and neutralization of pathogens. The protein encoded by this gene is a type I membrane receptor that mediates the endocytosis of glycoproteins by macrophages. The protein has been shown to bind high-mannose structures on the surface of potentially pathogenic viruses, bacteria, and fungi so that they can be neutralized by phagocytic engulfment.[provided by RefSeq, Sep 2015] |
| Alternative Names | MRC1 CLEC13D CLEC13DL MRC1L1 Macrophage mannose receptor 1 MMR C-type lectin domain family 13 member D C-type lectin domain family 13 member D-like Macrophage mannose receptor 1-like protein 1 CD206 |
| Molecular Weight(MW) | 190kDa (Observed band size: 190kDa) |
| Cellular Localization | Membrane |
WB
Various whole cell lysates were separated by 4-8% SDS-PAGE, and the membrane was blotted with anti-CD206/MRC1 antibody. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody. Lane 1: Mouse liver
WB
Western blot analysis of lysates from MUTZ-3 WT and knockdown cell. Cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with CD206/MRC1 PT0527R PT Rabbit mAb. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
IHC
Human colon was stained with anti-CD206/MRC1 rabbit antibody| Application Notes | WB:1:5000-1:20000 IHC:1:200-1:1000 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | -15°C to -25°C/1 year(Do not lower than -25°C) |
| Storage Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA |
