货号 | BAF3075 |
别名 | campomelic dysplasia, autosomal sex-reversal; CMD 1; CMD1; CMPD1; SRA1SRY (sex-determining region Y)-box 9 protein; SRY (sex determining region Y)-box 9; SRY-related HMG-box, gene 9; transcription factor SOX-9 | 全称 | Transcription Factor SOX9 |
反应种属 | Human |
应用 | Western Blot(0.1 µg/mL) Immunocytochemistry(5-15 µg/mL) |
目标/特异性 | In Western blots, approximately 5% cross-reactivity with recombinant human (rh) SOX10 is observed and less than 2% cross-reactivity with rhSOX2, rhSOX3, rhSOX7, rhSOX14, rhSOX17, and rhSOX21 is observed. |
使用方法 | Western Blot: 0.1 µg/mL Immunocytochemistry: 5-15 µg/mL |
来源 | Reconstitute at 0.2 mg/mL in sterile PBS. |
产品组分 |
供应商 | R&D Systems |
Entrez Gene IDs | 6662 (Human) |
纯化方式 | Antigen Affinity-purified |
免疫原 | E. coli-derived recombinant human SOX9 Met1-Lys151 Accession # P48436 |
生物活性 | Human |
标记 | Biotin |
溶解方法 | Reconstitute at 0.2 mg/mL in sterile PBS. |
背景 | Members of the large SOX family of transcription factors are widely conserved and at least 20 are found in mammals. Structurally SOX proteins exhibit a high mobility group (HMG) motif that binds the DNA minor groove. SOX family members are often found in multiprotein complexes that regulate their ability to affect transcription. SOX proteins play important roles in early development and are often used as markers to assess the differentiation of specific cell lineages. SRY (Sex determining Region Y)-box 9 (SOX9) belongs to the SOX (SRY-like HMG box) family of transcription factors with diverse roles in development. SOX9 is expressed in mesenchymal progenitors that give rise to chondrocytes and osteoblasts. SOX9 is also expressed in the central nervous system, neural crest, intestine, pancreas, and testis. Mutations in SOX9 are associated with defects in sex determination, cartilage and bone development, as well as abnormalities of the heart, kidneys, brain, gut, and pancreas. |
运输条件 | Blue Ice |
存放说明 | -20℃ |
参考文献 |
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