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首页  >  重组蛋白  >  Mouse Aaas Recombinant Protein
Aaas (基因名), Aladin (蛋白名), AAAS_MOUSE.
产品名称:

Mouse Aaas/ Aladin Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Adracalin

来源:
E.coli
种属:
Mouse
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.
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:
-
Mouse Aaas Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


通用注释


Sub Unit:
Interacts with NDC1, the interaction is required for nuclear pore localization.


Function:
Plays a role in the normal development of the peripheral and central nervous system.


Subcellular Location:
Nucleus Nuclear pore complex


该产品尚未在任何出版物中被引用。

[1].
"Mutant WD-repeat protein in triple-A syndrome."

[2].
"The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope."

[3].
"Molecular cloning and characterization of AAAS-V2, a novel splice variant of human AAAS."

[4].
"Proteomic analysis of the mammalian nuclear pore complex."

[5].
"Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene."

[6].
"Triple A or Allgrove syndrome. A case report with ophthalmic abnormalities and a novel mutation in the AAAS gene."

[7].
"Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome."

[8].
"The transmembrane nucleoporin NDC1 is required for targeting of ALADIN to nuclear pore complexes."

[9].
"Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism."

[10].
"A novel AAAS gene mutation (p.R194X) in a patient with triple A syndrome."
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