Mannose Receptor(CD206) Recombinant Rabbit Monoclonal Antibody [JF0953]
cat.: ET1702-04
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human, Mouse |
| Applications: | WB, IF-Cell, FC |
| Clonality: | Monoclonal |
| Clone number: | JF0953 |
| Form: | Liquid |
| Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term. |
| Storage buffer: | 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 166 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide within Human CD206 aa 1,407-1,456 / 1,456. |
| Positive control: | MOLT-4 cell lysate, Mouse lung tissue lysate, Human lung tissue lysate, HepG2 cell lysate, D3 cell lysate, HepG2. |
| Subcellular location: | Endosome membrane, Cell membrane. |
| Recommended Dilutions:
WB IF-Cell FC |
1:1,000-1:5,000 1:100 1:500-1:1,000 |
| Uniprot #: | SwissProt: P22897 Human | Q61830 Mouse |
| Alternative names: | bA541I19.1 C type lectin domain family 13 member D C-type lectin domain family 13 member D CD 206 CD206 CD206 antigen CLEC13D CLEC13DL Macrophage mannose receptor 1 Macrophage mannose receptor 1 like protein 1 Macrophage mannose receptor Mannose receptor C type 1 Mannose receptor C type 1 like 1 MMR MRC 1 MRC1 MRC1_HUMAN MRC1L1 OTTHUMP00000045206 |
Images
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Fig1:
Western blot analysis of Mannose Receptor(CD206) on different lysates with Rabbit anti-Mannose Receptor(CD206) antibody (ET1702-04) at 1/5,000 dilution. Lane 1: MOLT-4 cell lysate (20 µg/Lane) Lane 2: Mouse lung tissue lysate (40 µg/Lane) Predicted band size: 166 kDa Observed band size: 166 kDa Exposure time: 18 seconds; ECL: K1801; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1702-04) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
All lanes: Western blot analysis of CD206 with anti-CD206 antibody[JF0953] (ET1702-04) at 1:1,000 dilution. Lane 1: Wild-type HepG2 whole cell lysate (10 µg). Lane 2: CD206 knockdown HepG2 whole cell lysate (10 µg). Lane 3: CD206 knockdown HepG2 whole cell lysate (10 µg). ET1702-04 was shown to specifically react with CD206 in wild-type Hela cells. Weakened bands were observed when CD206 knockdown samples were tested. Wild-type and CD206 knockdown samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary antibody (ET1702-04, 1/1,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG-HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
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Fig3:
Western blot analysis of Mannose Receptor(CD206) on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1702-04, 1/1,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Human lung tissue lysate Lane 2: HepG2 cell lysate |
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Fig4:
Western blot analysis of Mannose Receptor(CD206) on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1702-04, 1/1,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Mouse lung tissue lysate Lane 2: D3 cell lysate |
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Fig5:
Immunocytochemistry analysis of HepG2 cells labeling Mannose Receptor(CD206) with Rabbit anti-Mannose Receptor(CD206) antibody (ET1702-04) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Mannose Receptor(CD206) antibody (ET1702-04) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. |
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Fig6:
Immunocytochemistry analysis of HepG2 cells labeling Mannose Receptor(CD206) with Rabbit anti-Mannose Receptor(CD206) antibody (ET1702-04) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Mannose Receptor(CD206) antibody (ET1702-04) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. |
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Fig7:
Flow cytometric analysis of HepG2 cells labeling Mannose Receptor(CD206). Cells were fixed and permeabilized. Then stained with the primary antibody (ET1702-04, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
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