SOX9/SRY-box 9

SOX9/SRY-box 9

• Gene Name: [SOX9]
• NCBI Gene ID: 6662
• Reactivity: Human
• Storage Conditions: Antibody with azide: store at 2 to 8 degree C.
  Antibody without azide: store at -20 to -80 degree C.
  Antibody is stable for 24 months. Non-hazardous. No MSDS required.
• Specificity: The specificity of this monoclonal antibody to its intended target was validated by HuProtTM Array, containing more than 19,000, full-length human proteins. 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. Nucleus (Potential). Campomelic dysplasia (CMD1) [MIM:114290]: Rare, often lethal, dominantly inherited, congenital osteo-chondrodysplasia, associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones, unusually small scapulae, deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate, micrognathia, flat face and hypertelorism are common.
• Other Gene Names: [SOX9; SOX9; CMD1; SRA1; CMPD1; SRXX2; SRXY10]
• Short Name: [SOX9/SRY-box 9]
• Other Product Names: [transcription factor SOX-9; Transcription factor SOX-9; transcription factor SOX-9; SRY-box transcription factor 9]
• NCBI GI Number: 4557853
• NCBI Accession Number: NP_000337.1
• NCBI GB Accession Number: NP_000337.1
• Uniprot Accession Number: P48436