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MNX1 Antibody

  • 货号：
    CSB-PA014692LA01HU
  • 规格：
    ￥440
  • 促销：
    小规格抗体限时一口价
  • 图片：
    • Western Blot
      Positive WB detected in: HEK293 whole cell lysate
      All lanes: MNX1 antibody at 2µg/ml
      Secondary
      Goat polyclonal to rabbit IgG at 1/50000 dilution
      Predicted band size: 41, 21 kDa
      Observed band size: 50 kDa
  • 其他：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) MNX1 Polyclonal antibody
  • Uniprot No.：
    P50219
  • 基因名：
    MNX1
  • 别名：
    HB 9 antibody; HB9 antibody; HLXB 9 antibody; HLXB9 antibody; Homeo box HB9 antibody; Homeobox HB9 antibody; Homeobox protein HB9 antibody; HOXHB9 antibody; MNX1 antibody; MNX1_HUMAN antibody; Motor neuron and pancreas homeobox 1 antibody; Motor neuron and pancreas homeobox protein 1 antibody; Sacral agenesis autosomal dominant (Currarino triad) antibody; SCRA 1 antibody; SCRA1 antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Recombinant Human Motor neuron and pancreas homeobox protein 1 protein (50-99AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated

    本页面中的产品，MNX1 Antibody (CSB-PA014692LA01HU)，的标记方式是Non-conjugated。对于MNX1 Antibody，我们还提供其他标记。见下表：

    可提供标记
    标记方式 货号 产品名称 应用
    HRP CSB-PA014692LB01HU MNX1 Antibody, HRP conjugated ELISA
    FITC CSB-PA014692LC01HU MNX1 Antibody, FITC conjugated
    Biotin CSB-PA014692LD01HU MNX1 Antibody, Biotin conjugated ELISA
  • 克隆类型：
    Polyclonal
  • 抗体亚型：
    IgG
  • 纯化方式：
    >95%, Protein G purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA, WB
  • 推荐稀释比：
    Application Recommended Dilution
    WB 1:500-1:5000
  • 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：
    Putative transcription factor involved in pancreas development and function.
  • 基因功能参考文献：
    1. MNX1 may directly regulate TrkB expression, which may increase their metastatic potential via suppression of anoikis and enhanced adhesion to the ECM. PMID: 30066929
    2. Pathogenic variants in MNX1 were detected in 28% of all CS cases and 25% of sporadic cases. The clinical phenotype was variable in patients with and without pathogenic variants; no significant genotype-phenotype correlation was observed. PMID: 29401559
    3. Findings identify RGS12 as a candidate tumor-suppressor gene in AA prostate cancer, which acts by decreasing expression of AKT and MNX1, establishing a novel oncogenic axis in this disparate disease setting. PMID: 28611045
    4. MNX1 as a novel targetable oncogene increased in African-American (AA) prostate cancer that is associated with aggressive disease. PMID: 27578002
    5. Findings demonstrated for the first time that lncRNA MNX1-AS1 functions as an oncogene in ovarian cancer. PMID: 28414551
    6. The results illustrated miR-200a and miR-141 could inhibit the expression of Hlxb9 by binding to its mRNA 3'UTR. Furthermore, the expression of miR-200a and miR-141 was almost reciprocal to that of Hlxb9. Overexpression of miR-200a and miR-141 downregulated the expression of pancreatic progenitor cell markers Hlxb9 PMID: 26801823
    7. The nuclear positioning of the HLXB9 gene was monitored at different stages. PMID: 25136833
    8. study reports the results of MNX1 mutational screening in a series of 28 cases suspected having Currarino Syndrome and characterization of 10 novel mutations PMID: 24095820
    9. NKX2-2 and MNX1 are etiological genes for neonatal diabetes. PMID: 24411943
    10. Both pHLXB9 and active GSK-3beta are elevated in beta cells with menin knockdown, in MEN1-associated beta cell tumors (insulinomas) PMID: 24425879
    11. study describes a Norwegian family with typical Currarino syndrome in which a heterozygous deletion removes the entire MNX1 gene but no other known genes; also report MNX1 mutations in 3other Norwegian families and confirm that the GCC12 repeat (c.373_375[12]) is a normal allelic variant PMID: 23370340
    12. HB9 binds to the prostaglandin E receptor 2 promoter and inhibits intracellular cAMP mobilization in leukemic cells. PMID: 23048027
    13. a new HLXB9 gene mutation identified in a Chinese family with members suffering from Currarino syndrome PMID: 21960426
    14. two novel mutations in the MNX1 gene in cases with Currarino syndrome PMID: 22820079
    15. 2 previously described mutations, 1 de novo nonsense mutation (p.Gln212X) & 1 maternally inherited frameshift mutation (p.Pro18ProfsX38)were found among 14 Currarino syndrome patients with presacral tumors. PMID: 21763840
    16. Hypermethylation of HLXB9 results in loss of expression and is associated with acute lymphoblastic leukemia. PMID: 21069786
    17. HLXB9 is overexpressed in patients with infantile acute myeloid leukemia. PMID: 19446746
    18. Incomeplete Curarino syndrome with more advantageous prognosis with autosomal domiant pattern homebox gene HLXBV9 mutation. PMID: 20146075
    19. study reports on the MNX1 mutations in a family segregating Currarino syndrome (CS) & 3 sporadic CS patients & on clinical characteristics of the affected individuals PMID: 19853743
    20. mutation in the HLXB9 transcription factor causes an autosomal dominant form of sacral agenesis PMID: 11940082
    21. The chromosomal rearrangements of the HLXB9 protein locus at 7q36 were not detected in Hodgkin lymphoma cells unlike acute myeloid leukemia subsets expressing HLXB9. PMID: 15772702
    22. High incidence of t(7;12)(q36;p13) in infant myeloid leukemia is associated with ectopic expression of HLXB9. PMID: 16646086
    23. This study confirms that familial Currarino syndrome (CS) patients in Korea have the same genetic background as other ethnicities and reaffirms the phenotype variability among CS patients with the same mutation. PMID: 17612791
    24. report 23 novel mutations in 26 patients among a series of 50 index cases with Currarino syndrome PMID: 18449898
    25. MNX1-ETV6 fusion gene in an acute megakaryoblastic leukemia. PMID: 18940475
    26. Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias PMID: 19212340

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  • 相关疾病：
    Currarino syndrome (CURRAS)
  • 亚细胞定位：
    Nucleus.
  • 组织特异性：
    Expressed in lymphoid and pancreatic tissues.
  • 数据库链接：

    HGNC: 4979

    OMIM: 142994

    KEGG: hsa:3110

    STRING: 9606.ENSP00000252971

    UniGene: Hs.37035