MNX1 Antibody, HRP conjugated
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中文名稱：MNX1兔多克隆抗體, HRP偶聯
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貨號：CSB-PA014692LB01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) MNX1 Polyclonal antibody
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Uniprot No.：
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基因名：MNX1
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別名：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
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human Motor neuron and pancreas homeobox protein 1 protein (50-99AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：HRP
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Protein G purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產品提供形式：Liquid
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應用范圍：ELISA
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Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：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.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：Putative transcription factor involved in pancreas development and function.
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基因功能參考文獻：
- MNX1 may directly regulate TrkB expression, which may increase their metastatic potential via suppression of anoikis and enhanced adhesion to the ECM. PMID: 30066929
- 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
- 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
- MNX1 as a novel targetable oncogene increased in African-American (AA) prostate cancer that is associated with aggressive disease. PMID: 27578002
- Findings demonstrated for the first time that lncRNA MNX1-AS1 functions as an oncogene in ovarian cancer. PMID: 28414551
- 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
- The nuclear positioning of the HLXB9 gene was monitored at different stages. PMID: 25136833
- 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
- NKX2-2 and MNX1 are etiological genes for neonatal diabetes. PMID: 24411943
- Both pHLXB9 and active GSK-3beta are elevated in beta cells with menin knockdown, in MEN1-associated beta cell tumors (insulinomas) PMID: 24425879
- 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
- HB9 binds to the prostaglandin E receptor 2 promoter and inhibits intracellular cAMP mobilization in leukemic cells. PMID: 23048027
- a new HLXB9 gene mutation identified in a Chinese family with members suffering from Currarino syndrome PMID: 21960426
- two novel mutations in the MNX1 gene in cases with Currarino syndrome PMID: 22820079
- 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
- Hypermethylation of HLXB9 results in loss of expression and is associated with acute lymphoblastic leukemia. PMID: 21069786
- HLXB9 is overexpressed in patients with infantile acute myeloid leukemia. PMID: 19446746
- Incomeplete Curarino syndrome with more advantageous prognosis with autosomal domiant pattern homebox gene HLXBV9 mutation. PMID: 20146075
- 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
- mutation in the HLXB9 transcription factor causes an autosomal dominant form of sacral agenesis PMID: 11940082
- 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
- High incidence of t(7;12)(q36;p13) in infant myeloid leukemia is associated with ectopic expression of HLXB9. PMID: 16646086
- 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
- report 23 novel mutations in 26 patients among a series of 50 index cases with Currarino syndrome PMID: 18449898
- MNX1-ETV6 fusion gene in an acute megakaryoblastic leukemia. PMID: 18940475
- Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias PMID: 19212340
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相關疾?。?/div>Currarino syndrome (CURRAS)亞細胞定位：Nucleus.組織特異性：Expressed in lymphoid and pancreatic tissues.數據庫鏈接：
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