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SOX9/SRY-box 9

CAT: 0544-MBS4381260-01Size: 0.02 mg (With BSA & Azide at 0.2mg/mL)Dry Ice: NoHazardous: No
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CAT#:0544-MBS4381260-01Size:0.02 mg (With BSA & Azide at 0.2mg/mL)
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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

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