| No | Size | Price | Availability | |
| ARP6662-61 | 50ul | 1500.00 | In Stock |  |
| ARP6662-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 6662 |
| Isotype: | IgG | Swiss Prot: | P48436 |
| purity: | Affinity purification |
| Background: |
| SOX9 Plays an important role in the normal skeletal development. May regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. Defects in SOX9 are the cause of campomelic dysplasia (CMD1). |
| Reactivity | Human, Mouse |
| Tested applications | WB IHC IF ICC |
| Clonality | Polyclonal Antibody |
| Calculated MW | 56 kDa |
| Recommended Dilutions |
WB 1:500-1:2000
IHC 1:50-1:200
IF 1:100-1:500
ICC 1:100-1:500
|
| Immunogen | A synthetic peptide derived from human SOX9 |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | CMD1, CMPD1, SOX9, SRA1, SRY (sex determining region Y)-box 9, SRY (sex-determining region Y)-box 9 protein, SRY-related HMG-box, gene 9, Transcription factor SOX-9, transcription factor SOX9 |
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