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AGRN (基因名), Agrin (蛋白名), agrin_human.
产品名称:

Human AGRN/ Agrin Recombinant Protein
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货号:

R1303h

商标:
EIAab®
监管等级:
别名:

AGRIN

序列号:
O00468
来源:
E.coli
种属:
Human
标签:
His
序列:
311-459aa
预估分子量:
16.39 kDa (monomer)
纯度:
Greater than 92% 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:
Neurosciences
Human AGRN Protein
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Human AGRN 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 AGRN Protein
Recombinant human AGRN protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 1p36.33 by HGNC 1p36.33 by Entrez Gene 1p36.33 by Ensembl
AGRN 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:
Monomer (By similarity). Interacts (N-terminal subunit) with TGF-beta family members, BMP2 AND BMP4; the interactions inhibit the activity of these growth factors. Interacts with TGFB1; the interaction enhances the activity of TGFB1 (By similarity). Component of the AGRN-LRP4 complex that consists of a tetramer of two AGRN-LRP4 heterodimers. Interacts (via the laminin G-like 3 domain) directly with LRP4; the interaction is required for activation of MUSK and clustering of AChR and requires the 'z8' insert present in the z(+8) isoforms. Interacts with DAG1; the interaction is influenced by cell surface glycosaminoglycans and by alternative splicing of AGRN.


功能:
Agrin C-terminal 22 kDa fragment: this released fragment is important for agrin signaling and to exert a maximal dendritic filopodia-inducing effect. All 'z' splice variants (z+) of this fragment also show an increase in the number of filopodia.


亚细胞位置:
Isoform 2 Cell junction Synapse Cell membrane Single-pass type II membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Identification of an agrin mutation that causes congenital myasthenia and affects synapse function."

[2].
"Primary structure and high expression of human agrin in basement membranes of adult lung and kidney."

[3].
"Agrin binds to the nerve-muscle basal lamina via laminin."

[4].
"Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy."

[5].
"LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin."

[6].
"Proteomics characterization of extracellular space components in the human aorta."

[7].
"Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome."

[8].
"Agrin and CD34 immunohistochemistry for the discrimination of benign versus malignant hepatocellular lesions."

[9].
"Amyloid beta induces cellular relocalization and production of agrin and glypican-1."

[10].
"Agrin signalling contributes to cell activation and is overexpressed in T lymphocytes from lupus patients."
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