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Rabbit Polyclonal STT3A Antibody

  • 中文名: STT3A抗体
  • 别    名: Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A, Oligosaccharyl transferase subunit STT3A, STT3-A, 2.4.99.18, B5, Integral membrane protein 1, Transmembrane protein TMC, STT3A, ITM1, TMC
货号: IPDX34329
Price: ¥1180
数量:
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验证与应用

应用及物种
WB 1/2000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 咨询技术 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesDolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A, Oligosaccharyl transferase subunit STT3A, STT3-A, 2.4.99.18, B5, Integral membrane protein 1, Transmembrane protein TMC, STT3A, ITM1, TMC
Entrez GeneID3703
WB Predicted band size80.5kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman, Mouse
ImmunogenThis STT3A antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 476-507 amino acids from the Central region of human STT3A.

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参考文献

以下是关于STT3A抗体的3篇示例参考文献(注:文献为虚构示例,实际文献请通过学术数据库查询):

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1. **文献名称**:*STT3A-mediated N-glycosylation of PD-L1 promotes immune evasion in melanoma*

**作者**:Chen L, et al.

**摘要**:本研究通过STT3A抗体进行免疫沉淀和蛋白质印迹分析,发现STT3A通过调控PD-L1的N-糖基化修饰增强其稳定性,从而抑制T细胞抗肿瘤活性,为靶向STT3A的癌症免疫治疗提供依据。

2. **文献名称**:*STT3A regulates apoptosis via glycosylation of BCL-2 family proteins*

**作者**:Wang X, et al.

**摘要**:利用STT3A抗体敲低实验发现,STT3A缺失导致内质网应激相关蛋白(如BAX)糖基化异常,进而诱导细胞凋亡,提示其在神经退行性疾病中的潜在作用。

3. **文献名称**:*High STT3A expression correlates with poor prognosis in gastric cancer*

**作者**:Tanaka R, et al.

**摘要**:通过免疫组化(使用STT3A抗体)分析胃癌组织样本,发现STT3A高表达与肿瘤转移和患者生存期缩短显著相关,表明其作为预后标志物的潜力。

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**建议**:如需真实文献,可通过PubMed或Google Scholar搜索关键词“STT3A antibody”、“STT3A function”或结合具体研究领域(如癌症、糖基化)进一步筛选。

背景信息

The STT3A antibody targets the STT3A protein, a catalytic subunit of the oligosaccharyltransferase (OST) complex located in the endoplasmic reticulum (ER). The OST complex mediates N-linked glycosylation, a critical post-translational modification where oligosaccharides are attached to asparagine residues of nascent polypeptides. This process is essential for protein folding, quality control, and cellular interactions. STT3A, along with its paralog STT3B, represents one of two major OST isoforms in mammals. While STT3A primarily acts co-translationally during protein synthesis, STT3B facilitates post-translational glycosylation of skipped sites. Dysregulation of STT3A is implicated in diseases such as cancer, congenital disorders of glycosylation (CDGs), and neurodegenerative conditions. Antibodies against STT3A are widely used in research to study ER-associated glycosylation mechanisms, protein trafficking, and disease pathogenesis. They enable detection of STT3A expression levels, subcellular localization via immunofluorescence or immunohistochemistry, and functional studies through knockdown or inhibition. Commercial STT3A antibodies are typically validated in Western blotting, immunoprecipitation, and ELISA, with applications spanning cell biology, oncology, and biomarker discovery. Recent studies also explore its role in immune evasion by pathogens and therapeutic targeting of glycosylation pathways.

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