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FIGURE: 1 / 2
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Positive control: Mouse embryonic brain
Cellular location: Nuclear.
This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: HMG box transcription factor SOX-14; SOX14; SRY (sex determining region Y)-box 14; SRY box 14; SRY-box 14; SRY-box containing gene 14; unnamed protein product
Gene Aliases: SOX28
UniProt ID: (Human) O95416, (Mouse) Q04892
Entrez Gene ID: (Human) 8403, (Rat) 300954, (Mouse) 20669
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