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- bs-16228P
- 2025年10月16日
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500ug
| 产品编号 | bs-16228P |
| 英文名称 | GALNTL5 Antibody Blocking Peptide |
| 中文名称 | GalNAc-TL5蛋白封闭多肽 |
| 英文别名 | GalNAc-T15; GALNACT19; GALNT15; GALNTL5; GLTL5_HUMAN; Polypeptide GalNAc transferase 15; pp-GaNTase 15; Protein-UDP acetylgalactosaminyltransferase 15; Putative polypeptide N-acetylgalactosaminyltransferase-like protein 5; UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase 15; UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5. |
| 纯化方法 | HPLC |
| 亚细胞定位 | Golgi apparatus membrane. |
| 组织特异性 | Expressed in testis. |
| 相似性 | Belongs to the glycosyltransferase 2 family. GalNAc-T subfamily. |
| 功能 | May catalyze the initial reaction in O-linked oligosaccharide biosynthesis, the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor. |
| 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 | GalNAc-TL4 utilizes manganese and calcium as cofactors and is expressed in testis. GalNAc-TL5 may assist with the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on protein receptors and likely catalyzes the initial reaction in O-linked oligosaccharide biosynthesis. Unlike other members of the GalNAc-T subfamily, GalNAc-TL5 does not contain a C-terminal ricin B-type lectin domain. GalNAc-TL5 contains two conserved domains located in its glycosyltransferase region. The N-terminal domain, also known as domain A or GT1 motif, may be involved in manganese coordination and substrate binding while the C-terminal domain, also known as domain B or Gal/GalNAc-T motif, is likely involved in catalytic reactions and UDP-Gal binding. GalNAc-TL5 exists as two alternatively spliced isoforms. |
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文献和实验or from the literature are missing. In this article, processing parameters for DNA, peptide, antibody, and carbohydrate microarrays are outlined. The applicability of the model experiments is demonstrated and described in detail on the example of short oligonucleotides.
Synthesis and Probing of Membrane-bound Peptide Arrays
the stringency of the blocking conditions and make sure that the primary binding partner and detection reagent (e.g., antibody) are of high purity and are used in the highest possible dilution. Stage
Mapping Protein‐Protein Interactions with Phage‐Displayed Combinatorial Peptide Libraries
. Fack, F., Deroo, S., Kreis, S., and Muller, C.P. 2000. Heteroduplex mobility assay (HMA) pre‐screening: An improved strategy for the rapid identification of inserts selected from phage‐displayed peptide
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