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| Size | List Price | Price | Cart |
|---|---|---|---|
| 100 ug | $365.00 | Add to Cart |
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. It plays a role in the differentiation of lung epithelium. May also play a role in developing neural, gastrointestinal and cardiovascular tissues. Defects in FOXP2 are the cause of speech-language disorder 1 (SPCH1); also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Affected individuals have a severe impairment in the selection and sequencing of fine orofacial movements, which are necessary for articulation |
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FOXP2 (dilution: 2.5 µg/ml) staining of paraffin embedded Human Prostate. Steamed antigen retrieval with citrate buffer pH 6, AP-staining Protocol on Data-sheet.
FOXP2 (dilution: 2.5 µg/ml) staining of paraffin embedded Human Prostate. Steamed antigen retrieval with citrate buffer pH 6, AP-staining Protocol on Data-sheet.
FOXP2 (dilution: 0.3µg/ml) staining of Human Brain (cerebellum) lysate (35µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
FOXP2 (dilution: 0.3µg/ml) staining of Human Brain (cerebellum) lysate (35µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.