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