Anti-SOX9 / SRY-box 9 Monoclonal Antibody (Clone: SOX9/2287R)
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.
Product Specifications
Product Name Alternative
Gene Name
SOX9
Gene ID
6662
UniProt
P48436
Host
Rabbit
Reactivity
Human
Immunogen
Recombinant human full-length SOX9 protein
Clonality
Monoclonal
Clone
SOX9/2287R
Applications
ELISA, WB
Components
Storage Conditions
Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous.
Applications Notes
ELISA (For coating, order antibody without BSA) ; , Western Blot (1-2ug/ml) ;
Isotype
Rabbit IgG
Explore Other Products
Browse additional items from our catalog