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MNX1 (基因名), Motor neuron and pancreas homeobox protein 1 (蛋白名), MNX1_HUMAN.
产品名称:

Human MNX1/ Motor neuron and pancreas homeobox protein 1 Recombinant Protein
运动神经元和胰腺同源异型盒蛋白1

货号:

R14435h

商标:
EIAab®
监管等级:
别名:

Homeobox protein HB9, HLXB9

序列号:
P50219
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human MNX1 Protein
规格 & 价格: cart
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Human MNX1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 7q36.3 by HGNC 7q36.3 by Entrez Gene 7q36.3 by Ensembl
MNX1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Putative transcription factor involved in pancreas development and function.


亚细胞位置:
Nucleus


该产品尚未在任何出版物中被引用。

[1].
"MNX1 (HLXB9) mutations in Currarino patients."

[2].
"Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene."

[3].
"A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis."

[4].
"A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues."

[5].
"Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype."

[6].
"Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias."

[7].
"Three-way complex translocations in infant acute myeloid leukemia with t(7;12)(q36;p13): the incidence and correlation of a HLXB9 overexpression."

[8].
"Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation."

[9].
"Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome."

[10].
"HLXB9 homeobox gene and caudal regression syndrome."
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