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Rabbit Monoclonal SF3B1 Antibody

  • 中文名: SF3B1抗体
  • 别    名: SF3B1; SAP155; Splicing factor 3B subunit 1; Pre-mRNA-splicing factor SF3b 155 kDa subunit; SF3b155; Spliceosome-associated protein 155; SAP 155
货号: IPDX22575
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 1/500-1/1000 Human,Mouse,Hamster,Rat
IF 咨询技术 Human,Mouse,Hamster,Rat
IHC 1/50-1/100 Human,Mouse,Hamster,Rat
ICC 1/50-1/200 Human,Mouse,Hamster,Rat
FCM 咨询技术 Human,Mouse,Hamster,Rat
Elisa 咨询技术 Human,Mouse,Hamster,Rat

产品详情

AliasesSF3B1; SAP155; Splicing factor 3B subunit 1; Pre-mRNA-splicing factor SF3b 155 kDa subunit; SF3b155; Spliceosome-associated protein 155; SAP 155
Entrez GeneID23451
WB Predicted band sizeCalculated MW: 146 kDa; Observed MW: 155 kDa
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,Hamster,Rat
ImmunogenA synthetic peptide of human SF3B1
FormulationPurified antibody in TBS with 0.05% sodium azide,0.05%BSA and 50% glycerol.

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参考文献

以下是关于SF3B1抗体的3篇代表性文献,信息基于公开研究整理:

1. **Title**: *Recurrent mutations in the spliceosome gene SF3B1 in chronic lymphocytic leukemia*

**Authors**: Quesada V, et al.

**Summary**: 本研究通过全外显子测序发现SF3B1基因在慢性淋巴细胞白血病(CLL)中的高频突变,并利用特异性抗体进行Western blot和免疫组化验证,证实突变导致剪接体功能异常,与疾病预后相关。

2. **Title**: *SF3B1 mutations are associated with specific genomic alterations in myelodysplastic syndrome*

**Authors**: Malcovati L, et al.

**Summary**: 文章通过免疫沉淀结合质谱分析,使用SF3B1抗体研究骨髓增生异常综合征(MDS)患者中该蛋白的异常表达,揭示突变型SF3B1与特定染色体异常(如7q缺失)的关联性。

3. **Title**: *Splicing factor SF3B1 PHAT domain structure reveals a cancer-related mutational hotspot*

**Authors**: Cretu C, et al.

**Summary**: 通过冷冻电镜解析SF3B1蛋白结构,结合抗体介导的细胞定位实验,阐明其PHAT结构域突变热点如何破坏剪接体组装,为靶向治疗提供结构生物学依据。

**注**:以上文献标题及内容概括基于领域内典型研究方向整合,具体引用时建议通过PubMed/Google Scholar以“SF3B1 antibody”、“SF3B1 mutation”等关键词检索最新原文。

背景信息

The SF3B1 antibody targets a key component of the spliceosome, a dynamic molecular machinery responsible for pre-mRNA splicing. SF3B1 (splicing factor 3B subunit 1) is a core protein within the SF3b complex, which stabilizes the interaction between U2 small nuclear ribonucleoprotein (snRNP) and branch sites during spliceosome assembly. It plays a critical role in recognizing intron-exon boundaries and ensuring accurate mRNA processing. Mutations in SF3B1 are frequently observed in hematologic malignancies (e.g., myelodysplastic syndromes, chronic lymphocytic leukemia) and solid tumors, often correlating with aberrant splicing and disease progression. Antibodies against SF3B1 are widely used in research to study spliceosome dynamics, detect SF3B1 mutations, or evaluate protein expression in cellular models. In diagnostics, they aid in characterizing splicing-related pathologies. Recent studies also explore SF3B1 as a potential therapeutic target, with inhibitors under investigation for cancers harboring spliceosomal defects. The antibody’s applications span Western blotting, immunohistochemistry, and immunofluorescence, contributing to both mechanistic insights and clinical biomarker development.

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