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TBX20 Antibody

  • 中文名称：
    TBX20兔多克隆抗体
  • 货号：
    CSB-PA234177
  • 规格：
    ￥1100
  • 图片：
    • Gel: 8%SDS-PAGE, Lysate: 40 μg, Lane: K562 cells, Primary antibody: CSB-PA234177(TBX20 Antibody) at dilution 1/500, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 40 seconds
  • 其他：

产品详情

  • Uniprot No.：
    Q9UMR3
  • 基因名：
    TBX20
  • 别名：
    T-box 20 antibody; T-box protein 20 antibody; T-box transcription factor TBX20 antibody; Tbox 20 antibody; tbx20 antibody; TBX20_HUMAN antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse
  • 免疫原：
    Fusion protein of Human TBX20
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated
  • 抗体亚型：
    IgG
  • 纯化方式：
    Antigen affinity purification
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA,WB
  • 推荐稀释比：
    Application Recommended Dilution
    ELISA 1:2000-1:5000
    WB 1:500-1:2000
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

产品评价

靶点详情

  • 功能：
    Acts as a transcriptional activator and repressor required for cardiac development and may have key roles in the maintenance of functional and structural phenotypes in adult heart.
  • 基因功能参考文献：
    1. TBX20 can be considered a KCNH2-modifying gene. PMID: 28049825
    2. This study firstly links TBX20 loss-of-function mutation to familial tetralogy of Fallot or sporadic persistent truncus arteriosus, providing novel insight into the molecular pathogenesis of Congenital heart disease. PMID: 28553164
    3. results showed that the TBX20 gene is not the major gene affecting nonsyndromic congenital heart disease development PMID: 28525297
    4. chromatin analysis reveals that endocardial TBX20 has roles in septation PMID: 27348591
    5. The current study associated TBX20 haploinefficiency with isolated Dilated cardiomyopathy (DCM), and expanded upon the mutational spectrum of TBX20 associated with DCM and congenital heart disease (CHD), which provides novel insight into the molecular mechanism of DCM and CHD, suggesting potential implications for early personalized treatment of these diseases. PMID: 27510170
    6. Silencing of TBX20 in rat myocardial and human embryonic kidney cells significantly inhibited cell proliferation, induced cell apoptosis and led to G2/M cell cycle arrest. PMID: 27572266
    7. rs3999950 may be associated with congenital heart disease, and TBX20 may predispose children to the defect. PMID: 27323105
    8. Among the 8 SNPs identified, 6 are in strong linkage disequilibrium and the minor alleles are associated with lower CHD risk. The minor alleles have lower transcriptional activity than major alleles in both human heart tissues and three cell lines. TBX20 minor alleles may exhibit higher binding affinity with certain transcription repressors. PMID: 27034249
    9. Cardiac TBX20 expression showed a negative correlation with LVEF and a positive correlation with left ventricular end-systolic volume. No significant difference in TBX20 CNVs and promoter methylation was observed between IDCM patients and control group PMID: 26895318
    10. The mutation markedly reduced the synergistic activation of TBX20 with NKX2-5 or GATA4. PMID: 26118961
    11. We report three missense mutations (Y309D, T370O, and M395R) within the transcriptional activator domain of human TBX20 that were associated with atrial septal defect PMID: 25834824
    12. Data showed that the TC genotype of SNP rs3999941 and AC genotype of the new SNP c.657A>C in the TBX20 gene may be risk factors for CHD. PMID: 25487630
    13. TBX20 loss-of-function mutation contributes to double outlet right ventricle PMID: 25625280
    14. A novel TBX20 mutation, c.526G>A (p.D176N), was identified and co-segregated in all affected members in this family of three generations with atrial septal defects. PMID: 25183037
    15. Tbx20 regulated PPAR-gamma expression and protected the vascular endothelial cells from oxidized low-density lipoprotein -induced injury. PMID: 24247152
    16. Tbx20 functions as an important regulator of estrogen-mediated cardiomyocyte protection during oxidative stress. PMID: 23871353
    17. Study identified one novel heterozygous sequence variant within the proximal promoter region of TBX20 gene in a ventricular septal defects patient, which inhibited transcriptional activities of TBX20 gene promoter; data provide new information to help understanding of genetic causes and molecular mechanisms of congenital heart disease. PMID: 22465533
    18. This novel interaction between TBX20b and MKLN1 may help elucidate new regulatory mechanisms within heart development. PMID: 21586270
    19. Found tertiary hydrophobic interactions within the mutant TBX20 T-box of Ostium secundum atrial septal defect subjects were significantly altered leading to a more dynamic structure of the protein. PMID: 19762328
    20. Our findings are the first to link TBX20 mutations to human pathology PMID: 17668378
    21. analysis of TBX20 in human hearts and its regulation by TFAP2 PMID: 18275040
    22. findings provide the first insight into TBX20 mutations for tetrology of fallot and anomalous pulmonary venous connection PMID: 18834961
    23. These data highlight unique features of Tbx20 and suggest mechanistic ways in which cardiac T-box factors might interact synergistically and/or competitively within the cardiac regulatory network. PMID: 19414016

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  • 相关疾病：
    Atrial septal defect 4 (ASD4)
  • 亚细胞定位：
    Nucleus.
  • 数据库链接：

    HGNC: 11598

    OMIM: 606061

    KEGG: hsa:57057

    STRING: 9606.ENSP00000386170

    UniGene: Hs.404167