- ￥880
- Bioss
- bs-14995P
- 2025年10月16日
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- 详细信息
- 技术资料
- 规格：
500ug
| 产品编号 | bs-14995P |
| 英文名称 | TENT5A Antibody Blocking Peptide |
| 中文名称 | FAM46A蛋白封闭多肽 |
| 英文别名 | C6orf37; Chromosome 6 open reading frame 37; D930050G01Rik; FA46A_HUMAN; FAM46A; Family with sequence similarity 46, member A; FLJ20037; FLJ31495; HBV X-transactivated gene 11 protein; HBV XAg-transactivated protein 11; Hypothetical protein LOC55603; OTTHUMP00000016782; Protein FAM46A; Retinal expressed gene C6orf37; RGD1311381; XTP11. |
| 纯化方法 | HPLC |
| 组织特异性 | Widely expressed, with preferential expression observed in the retina compared to other ocular tissues. |
| 相似性 | Belongs to the FAM46 family. |
| 保存条件 | Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 背景资料 | Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The FAM46A gene product has been provisionally designated FAM46A pending further characterization. |
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TENT5A Antibody Blocking Peptide(bs-14995P)-500ug
￥880
