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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
详见官方网站
- 亚型:
详见官方网站
- 形态:
冻干粉/浓缩液
- 保存条件:
-20℃
- 克隆性:
多克隆
- 标记物:
详见说明书
- 适应物种:
详见说明书
- 宿主:
详见官方网站
- 应用范围:
详见官方网站
- 浓度:
1mg/ml
- 抗体英文名:
Alpha-N-acetylgalactosaminidase
- 规格:
100ug,200ug,1mg
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文献和实验Biochemical Characterization of a Testis-Predominant Isoform of N-Alpha Acetyltransferase
N-alpha protein acetylation, catalyzed by N-alpha acetyltransferase complex, is a common protein �modification process in eukaryotic cells. Despite its widespread occurrence, the biological significance of this modification process
A Fluorescence-Based Assay for Core 1 3Galactosyltransferase (T-Synthase) Activity
hydrolyzed by endo-α-N -acetylgalactosaminidase (O-glycosidase) releasing free 4-MU. Free 4-MU is highly fluorescent at pH 9.6–10 and can be easily measured by a fluorescent detector (Ex: 355 nm; Em: 460 nm). This fluorescence-based T-synthase assay is simple
that requires TNF receptor–1 (TNFR1) activity to stimulate c-Jun N-terminal kinase (JNK) activity and hence to activate AP-1 (Fig. 1). Direct treatment of macrophages with TNF-{alpha} also promoted the accumulation of miR-155, but this factor appeared
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