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OTX2 (基因名), Homeobox protein OTX2 (蛋白名), otx2_human.
产品名称:

Human OTX2/ Homeobox protein OTX2 Recombinant Protein
同源异形盒蛋白OTX2

货号:

R14438h

商标:
EIAab®
监管等级:
别名:

Orthodenticle homolog 2

序列号:
P32243
来源:
E.coli
种属:
Human
标签:
His
序列:
37-116aa
预估分子量:
8.8 kDa (monomer)
纯度:
Greater than 95% 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:
Development Biology
  • Human OTX2 Protein
  • Human OTX2 Protein
  • Human OTX2 Protein
规格 & 价格: cart
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Human OTX2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human OTX2 Protein
The PCR product of human OTX2 gene was determined by 1% Agarose stained with EB.
Human OTX2 Protein
Recombinant human OTX2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 14q22.3 by HGNC 14q22.3 by Entrez Gene 14q22.3 by Ensembl
OTX2 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:
Probably plays a role in the development of the brain and the sense organs. Can bind to the BCD target sequence (BTS): 5'-TCTAATCCC-3'.


亚细胞位置:
Nucleus


该产品尚未在任何出版物中被引用。

[1].
"A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency."

[2].
"Expression of the homeobox genes PAX6, OTX2, and OTX1 in the early human fetal retina."

[3].
"Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma."

[4].
"A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency."

[5].
"Polymorphisms in the homeobox gene OTX2 may be a risk factor for bipolar disorder."

[6].
"Chromosome locations of human EMX and OTX genes."

[7].
"OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium."

[8].
"OTX2 mutations contribute to the otocephaly-dysgnathia complex."

[9].
"A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve."

[10].
"Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype."
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