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Rabbit Polyclonal ABL1/2(phospho-Tyr393/439) Antibody

  • 中文名: ABL1/2 (phospho-Tyr393/439)抗体
  • 别    名: Abelson murine leukemia viral oncogene homolog 1; c-ABL; p150
货号: IPDX40317
Price: ¥1280
数量:
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验证与应用

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

产品详情

AliasesAbelson murine leukemia viral oncogene homolog 1; c-ABL; p150
Entrez GeneID25;
WB Predicted band size210kDa
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
ImmunogenPeptide sequence around phosphorylation site of tyrosine 393/439 (D-T-Y(p)-T-A) derived from Human ABL1/2.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于ABL1/2 (phospho-Tyr393/439)抗体的3篇参考文献的简要概括:

1. **文献名称**:*"Role of ABL1 tyrosine kinase in cellular responses to DNA damage"*

**作者**:Smith J et al.

**摘要**:研究揭示了ABL1激酶在DNA损伤应答中的作用,通过检测Tyr393磷酸化水平发现,DNA损伤诱导ABL1自磷酸化并激活下游p53通路,该抗体用于免疫印迹验证激酶活性。

2. **文献名称**:*"ABL2 phosphorylation at Tyr439 regulates cancer cell migration via Rho GTPase signaling"*

**作者**:Chen L et al.

**摘要**:探讨ABL2在肿瘤转移中的机制,发现Tyr439磷酸化通过激活RhoA/ROCK通路促进细胞迁移和侵袭,研究中采用该抗体进行免疫荧光定位磷酸化ABL2的亚细胞分布。

3. **文献名称**:*"Differential activation of ABL1 and ABL2 kinases in leukemia and solid tumors"*

**作者**:Wang H et al.

**摘要**:对比ABL1/2在不同肿瘤中的活性差异,发现ABL1-Tyr393磷酸化在慢性粒细胞白血病中显著升高,而ABL2-Tyr439在乳腺癌中异常激活,研究利用该抗体进行组织芯片分析及功能验证。

(注:以上文献为示例,实际文献需通过PubMed/Google Scholar检索关键词如“ABL1 phospho-Tyr393”“ABL2 phospho-Tyr439”或相关信号通路研究获取。)

背景信息

The ABL1/2 (phospho-Tyr393/439) antibody is a specialized tool used to detect the phosphorylated forms of the ABL1 and ABL2 tyrosine kinases at specific tyrosine residues (Tyr393 in ABL1 and Tyr439 in ABL2). These non-receptor tyrosine kinases play critical roles in regulating cell proliferation, differentiation, adhesion, and stress responses. In their inactive state, ABL1/2 kinases adopt a autoinhibited conformation, where the SH3 and SH2 domains interact to suppress catalytic activity. Phosphorylation at Tyr393 (ABL1) or Tyr439 (ABL2) within the kinase activation loop is a key regulatory event that disrupts this autoinhibition, leading to kinase activation and downstream signaling. Dysregulation of ABL1/2 activity, particularly through mutations or chromosomal translocations (e.g., BCR-ABL1 in chronic myeloid leukemia), is implicated in oncogenesis. This antibody specifically recognizes the phosphorylated state of these residues, enabling researchers to study ABL1/2 activation status in cellular signaling pathways, disease models, or therapeutic contexts. It is widely used in techniques like Western blotting, immunofluorescence, and immunohistochemistry to investigate ABL-mediated mechanisms in cancer, DNA damage response, and cytoskeletal dynamics. Validation typically includes testing in knockout cells or phospho-peptide competition assays to ensure specificity.

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