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- Bioss
- bs-13379P
- 2026年10月10日
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- 技术资料
- 规格：
500ug
| 产品编号 | bs-13379P |
| 英文名称 | GLT25D2 Antibody Blocking Peptide |
| 中文名称 | 糖基转移酶25结构域2/前胶原半乳糖基转移酶2封闭多肽 |
| 英文别名 | C1orf17; Glt25d2; Glycosyltransferase 25 family member 2; GT252_HUMAN; Hydroxylysine galactosyltransferase 2; Procollagen galactosyltransferase 2; RP11-498P10.2. |
| 纯化方法 | HPLC |
| 研究领域 | Signal Transduction > Metabolism > Amino Acids Signal Transduction > Protein Trafficking > ER Proteins |
| 亚细胞定位 | Endoplasmic reticulum lumen. |
| 组织特异性 | Expressed in brain and skeletal muscle. |
| 相似性 | Belongs to the glycosyltransferase 25 family. |
| 功能 | Has a beta-galactosyltransferase activity; transfers beta-galactose to hydroxylysine residues on collagen. |
| 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 | GLT25D2 is a 626 amino acid protein that localizes to endoplasmic reticulum lumen and belongs to the glycosyltransferase 25 family. Possessing beta-galactosyltransferase activity, GLT25D2 transports beta-galactose to hydroxylysine residues on collagen but lacks glucosyltransferase activity. GLT25D2 is expressed in skeletal muscle and brain, and is encoded by a gene located on human chromosome 1q25.3, a region associated with the hereditary prostate cancer (HPC1) locus. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes, comprises nearly 8% of the human genome and houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. |
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COLGALT2 | GLT25D2 Ab Blocking Peptide(bs-13379P)-500ug
￥880
