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- Bioss
- bs-15435R-BF594
- 2025年09月30日
- 产品信息以Bioss网站为准
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100ul
| 产品编号 | bs-15435R-BF594 |
| 英文名称 | HDX Rabbit pAb, BF594 conjugated |
| 中文名称 | BF594标记的高度发散同源异型盒蛋白抗体 |
| 英文别名 | CXorf43; D030011N01Rik; FLJ30678; Hdx; HDX_HUMAN; Highly divergent homeobox; MGC126769; MGC126771; OTTHUMP00000062139. |
| 产品应用 | ICC/IF=1:50-200, IF=1:100-500 Not yet tested in other applications. |
| 抗体来源 | Rabbit |
| 免疫原 | KLH conjugated synthetic peptide derived from human HDX |
| 亚型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 克隆类型 | Polyclonal |
| 浓度 | 1mg/ml |
| 储存液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 亚细胞定位 | Nucleus. |
| 相似性 | Contains 2 homeobox DNA-binding domains. |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 背景资料 | HDX (highly divergent homeobox) is a 690 amino acid nuclear protein that contains two homeobox DNA-binding domains. Existing as two alternatively spliced isoforms, the gene encoding HDX maps to the human X chromosome, which consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome leads to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. |
| 应用 | 推荐稀释比例 |
| {ICC/IF} | {1:50-200} |
| {IF} | {1:100-500} |
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HDX Rabbit pAb, BF594 conjugated(bs-15435R-BF594)-100ul
￥2980
