| Объем | 50 мкл | 
| Синонимы | CD99 antigen, 12E7, E2 antigen, Protein MIC2, T-cell surface glycoprotein E2, CD99, CD99, MIC2, MIC2X, MIC2Y | 
| Тип антител | Recombinant Antibody | 
| Species | Human | 
| UniProt ID | P14209 | 
| Иммуноген | A synthesized peptide | 
| Видовая специфичность | Human | 
| Применение | ELISA, WB, IHC, FC, Recommended dilution: WB:1:500-1:5000, IHC:1:50-1:500 | 
| Клональность | Monoclonal | 
| Изотип | Rabbit IgG | 
| Коньюгат | Non-conjugated | 
| Буффер | Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. | 
| Форма | Liquid | 
| Хранение | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. | 
| Метод очистки | Affinity-chromatography | 
| Области исследований | Immunology | 
| Аббревиатура | CD99 antigen | 
| Примечание | Involved in T-cell adhesion processes and in spontaneous rosette formation with erythrocytes. Plays a role in a late step of leukocyte extravasation helping leukocytes to overcome the endothelial basement membrane. Acts at the same site as, but independently of, PECAM1. Involved in T-cell adhesion processes (By similarity). | 
| Ссылка на страницу на сайте производителя | ссылка | 
Western Blot 
Positive WB detected in:Jurkat whole cell lysate 
All lanes:CD99 antibody at 0.8µg/ml 
Secondary 
Goat polyclonal to rabbit IgG at 1/50000 dilution 
Predicted band size: 28 KDa 
Observed band size: 28 KDa
 
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IHC image of CSB-RA004973A0HU diluted at 1:100 and staining in paraffin-embedded human pancreatic tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
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Overlay histogram showing Jurkat cells stained with CSB-RA004973A0HU (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min.The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4?.The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4?. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
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