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Product Name Recombinant Rabbit Anti-MAPRE3 Monoclonal Antibody Cat No. SLA1880M Chinese Name MAPRE3重组兔单抗 Alias MARE3_HUMAN; MAPRE3; EB1 protein family member 3 (EBF3); End-binding protein 3 (EB3); RP3; EB3; EBF3; EBF3-S; microtubule associated protein RP/EB family member 3 Host Species Rabbit Isotype IgG Clonality Monoclonal Clone No. 2A12 React Species Human,Mouse,Rat Applications WB (1:500-2000)
IHC-P (1:100-500)
IHC-F (1:100-500)
IF (1:100-500)
Flow-Cyt (1:50-100)
ICC/IF (1:50-200)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.Immunogen A synthesized peptide derived from human MAPRE3 Purification affinity purified by Protein A Predicted MW. 32 kDa Observed MW. 32 kDa Subcellular Location N/A Gene ID 22924 Swiss-Prot Q9UPY8 Storage 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.Background Plus-end tracking protein (+TIP) that binds to the plus-end of microtubules and regulates the dynamics of the microtubule cytoskeleton.Promotes microtubule growth.May be involved in spindle function by stabilizing microtubules and anchoring them at centrosomes. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Validation Images
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Figure 1. 25 ug total protein per lane of various lysates (see on figure) probed with MAPRE3 monoclonal antibody, unconjugated (SLA1880M) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r.t. for 60 min
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Figure 2. Paraformaldehyde-fixed, paraffin embedded Mouse Testicles; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with MAPRE3 Monoclonal Antibody, Unconjugated (SLA1880M) at 1:200 overnight at 4°C, followed by conjugation to the SL0295G-HRP and DAB (C-0010) staining
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Figure 3. Paraformaldehyde-fixed, paraffin embedded Rat Testicles; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with MAPRE3 Monoclonal Antibody, Unconjugated (SLA1880M) at 1:200 overnight at 4°C, followed by conjugation to the SL0295G-HRP and DAB (C-0010) staining
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Figure 4. Paraformaldehyde-fixed, paraffin embedded Mouse Cerebellum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with MAPRE3 Monoclonal Antibody, Unconjugated (SLA1880M) at 1:200 overnight at 4°C, followed by conjugation to the SL0295G-HRP and DAB (C-0010) staining
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Figure 5. Paraformaldehyde-fixed, paraffin embedded Rat Cerebellum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with MAPRE3 Monoclonal Antibody, Unconjugated (SLA1880M) at 1:200 overnight at 4°C, followed by conjugation to the SL0295G-HRP and DAB (C-0010) staining
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Figure 6. Paraformaldehyde-fixed, paraffin embedded Human Glioma; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with MAPRE3 Monoclonal Antibody, Unconjugated (SLA1880M) at 1:200 overnight at 4°C, followed by conjugation to the SL0295G-HRP and DAB (C-0010) staining
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Figure 7. Paraformaldehyde-fixed, paraffin embedded Human Cerebrum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with MAPRE3 Monoclonal Antibody, Unconjugated (SLA1880M) at 1:200 overnight at 4°C, followed by conjugation to the SL0295G-HRP and DAB (C-0010) staining
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Figure 8. The SH-SY5Y (H) cells were fixed with 4% PFA (10 min at r.t.) and then permeabilized with 90% ice-cold methanol for 20 min at -20℃,the cells then were incubated in 5%BSA to block non-specific protein-protein interactions (30 min at r.t.), followed by secondary antibody incubation for 40 min at room temperature. Primary Antibody (green):Rabbit Anti-MAPRE3 antibody (SLA1880M,1:100); Isotype Control (orange): Rabbit IgG (SL0295P). Blank control (black): PBS. Acquisition of 20,000 events was performed
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Figure 9. 4% Paraformaldehyde-fixed SH-SY5Y (H) cell; Triton X-100 at r.t. for 20 min; Antibody incubation with (MAPRE3) monoclonal Antibody, unconjugated (SLA1880M) 1:100, 90 min at 37°C; followed by conjugated Goat Anti-Rabbit IgG antibody (green, SL60295G-BF488) at 37°C for 90 min, DAPI (blue, C02-04002) was used to stain the cell nuclei. PBS instead of the primary antibody was used as the blank control
FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.
+86 571 56623320
[email protected]
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