at 1/500 dilution. Positive control: Lane1: NCCIT Lane2: MEF Lane3: HES
Fig2: ICC staining FPR1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig3: ICC staining FPR1 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig4: ICC staining FPR1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig5: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-FPR1 antibody. Counter stained with hematoxylin.
Fig6: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-FPR1 antibody. Counter stained with hematoxylin.
Fig7: Flow cytometric analysis of MCF-7 cells with FPR1 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black).
Product Name | FPR1 |
---|---|
Antibody Type | Primary Antibodies |
Product description |
|
Immunogen | Peptide |
Clonality | Polyclonal |
---|---|
Isotype | IgG |
Host Species | Rabbit |
Tested Applications | |
WB:1:500 ICC:1:50-1:200 IHC:1:50-1:100 FC:1:50-1:100 |
|
Species Reactivity | |
Concentration | 1 mg/mL. |
Alternative Names | fMet Leu Phe receptor antibody
fMet-Leu-Phe receptor antibody
FMLP antibody
fMLP receptor antibody
FMLPR antibody
Formyl peptide receptor 1 antibody
FPR 1 antibody
FPR antibody
FPR receptor antibody
FPR1 antibody
FPR1_HUMAN antibody
N formyl peptide chemoattractant receptor antibody
N formyl peptide receptor antibody
N formylpeptide chemoattractant receptor antibody
N-formyl peptide receptor antibody
N-formylpeptide chemoattractant receptor antibody
|
---|---|
Molecular Weight(MW) | 38 kDa |
Cellular Localization | Cell membrane. |
SwissProt ID | P21462 |
---|
at 1/500 dilution. Positive control: Lane1: NCCIT Lane2: MEF Lane3: HES
Fig2: ICC staining FPR1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig3: ICC staining FPR1 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig4: ICC staining FPR1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig5: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-FPR1 antibody. Counter stained with hematoxylin.
Fig6: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-FPR1 antibody. Counter stained with hematoxylin.
Fig7: Flow cytometric analysis of MCF-7 cells with FPR1 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black).
Positive Control | NCCIT, MEF, HES, Hela, HepG2, MCF-7, human tonsil tissue, human spleen tissue. |
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Application Notes | WB:1:500 ICC:1:50-1:200 IHC:1:50-1:100 FC:1:50-1:100 |
Form | Liquid |
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Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage Buffer | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
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