| Catalog_no | AP1503 |
| Product_name | Sox2 (phospho-Ser250/Ser251) rabbit pAb |
| Category | 抗原抗体 |
| Applications | WB |
| Reactivity | Human,Mouse |
| Size | 100μg/50μg/20μg |
| Price | 2200.00/1200.00/560.00 |
| Gene_name | SOX2 |
| Protein_name | Sox2 (Ser250/Ser251) |
| Human swiss prot no | 6657 |
| Human swiss prot no | P48431 |
| Mouse gene id | 20674 |
| Mouse swiss prot no | P48432 |
| immunogen | Synthesized phosho peptide around human Sox2 (Ser250 and Ser251) |
| Specificity | This antibody detects endogenous levels of Human Mouse Sox2 (phospho-Ser250 or Ser251) |
| Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
| Source | Rabbit |
| Dilution | WB 1:1000-2000 |
| Purification | The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. |
| Concentration | 1 mg/ml |
| Storage_stability | -20°C/1 year |
| othername | Transcription factor SOX-2 |
| Observed_band | 35KD |
| Background | SRY-box 2(SOX2) Homo sapiens This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008], |
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