E2A Monoclonal Antibody

    • 货号:YM0204
    • 应用:WB;FCM;ELISA
    • 种属:Human
      • 靶点:
      • E2A
      • 简介:
      • >>Signaling pathways regulating pluripotency of stem cells;>>Human T-cell leukemia virus 1 infection;>>Transcriptional misregulation in cancer
      • 基因名称:
      • TCF3
      • 蛋白名称:
      • Transcription factor E2-alpha
      • Human Gene Id:
      • 6929
      • Human Swiss Prot No:
      • P15923
      • Mouse Swiss Prot No:
      • P15806
      • 免疫原:
      • Purified recombinant fragment of human E2A expressed in E. Coli.
      • 特异性:
      • E2A Monoclonal Antibody detects endogenous levels of E2A protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Monoclonal, Mouse
      • 稀释:
      • WB 1:500 - 1:2000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
      • 纯化工艺:
      • Affinity purification
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • TCF3;BHLHB21;E2A;ITF1;Transcription factor E2-alpha;Class B basic helix-loop-helix protein 21;bHLHb21;Immunoglobulin enhancer-binding factor E12/E47;Immunoglobulin transcription factor 1;Kappa-E2-binding factor;Transcription facto
      • 分子量:
      • 68kD
      • 背景:
      • This gene encodes a member of the E protein (class I) family of helix-loop-helix transcription factors. E proteins activate transcription by binding to regulatory E-box sequences on target genes as heterodimers or homodimers, and are inhibited by heterodimerization with inhibitor of DNA-binding (class IV) helix-loop-helix proteins. E proteins play a critical role in lymphopoiesis, and the encoded protein is required for B and T lymphocyte development. Deletion of this gene or diminished activity of the encoded protein may play a role in lymphoid malignancies. This gene is also involved in several chromosomal translocations that are associated with lymphoid malignancies including pre-B-cell acute lymphoblastic leukemia (t(1;19), with PBX1), childhood leukemia (t(19;19), with TFPT) and acute leukemia (t(12;19), with ZNF384). Alternatively spliced transcript variants encoding multiple isoforms have bee
      • 功能:
      • disease:Chromosomal aberrations involving TCF3 are cause of forms of pre-B-cell acute lymphoblastic leukemia (B-ALL). Translocation t(1;19)(q23;p13.3) with PBX1; Translocation t(17;19)(q22;p13.3) with HLF. Inversion inv(19)(p13;q13) with TFPT.,function:Heterodimers between TCF3 and tissue-specific basic helix-loop-helix (bHLH) proteins play major roles in determining tissue-specific cell fate during embryogenesis, like muscle or early B-cell differentiation. Dimers bind DNA on E-box motifs: 5'-CANNTG-3'. Binds to the kappa-E2 site in the kappa immunoglobulin gene enhancer.,PTM:Phosphorylated following NGF stimulation.,similarity:Contains 1 basic helix-loop-helix (bHLH) domain.,subunit:Efficient DNA binding requires dimerization with another bHLH protein. Forms a heterodimer with ASH1 and TWIST2. Isoform E12 interacts with GRIPE and FIGLA (By similarity). Interacts with PTF1A and TGFB1I1.
      • 细胞定位:
      • Nucleus .
      • 组织表达:
      • Lymphoma,Muscle,PCR rescued clones,
      • 产品图片
      • Western Blot analysis using E2A Monoclonal Antibody against A549 (1), A431 (2), HeLa (3), PANC-1 (4) and PC-3 (5) cell lysate.
      • Flow cytometric analysis of A549 cells using E2A Monoclonal Antibody (green) and negative control (purple).