| No | Size | Price | Availability | |
| AMM145873-61 | 50ul | 1500.00 | In Stock |  |
| AMM145873-61 | 100ul | 2000.00 | In Stock | |
| Source: | Mouse | Gene Id: | 145873 |
| Isotype: | IgG1 | Swiss Prot: | Q0VG99 |
| purity: | Affinity chromatography |
| Background: |
| This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02). |
| Reactivity | Human |
| Tested applications | WB ELISA |
| Clonality | Monoclonal Antibody |
| Calculated MW | 42 kDa |
| Recommended Dilutions |
WB 1:500-1:2000
|
| Immunogen | A purified recombinant fragment of human MESP2 expressed in E. Coli |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | SCDO2, bHLHc6 |
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