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A1CF (基因名), APOBEC1 complementation factor (蛋白名), A1CF_HUMAN.
产品名称:

Human A1CF/ APOBEC1 complementation factor Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

APOBEC1-stimulating protein, ACF, ASP

序列号:
Q9NQ94
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 A1CF Protein
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Human A1CF Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


基因位点
Cytogenetic band: 10q11.23 by HGNC 10q11.23 by Entrez Gene 10q11.23 by Ensembl
A1CF 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:
Part of the apolipoprotein B mRNA editing complex with APOBEC1. Interacts with TNPO2; TNPO2 may be responsible for transport of A1CF into the nucleus. Interacts with SYNCRIP. Interacts with CELF2/CUGBP2.


功能:
Essential component of the apolipoprotein B mRNA editing enzyme complex which is responsible for the postranscriptional editing of a CAA codon for Gln to a UAA codon for stop in APOB mRNA. Binds to APOB mRNA and is probably responsible for docking the catalytic subunit, APOBEC1, to the mRNA to allow it to deaminate its target cytosine. The complex also protects the edited APOB mRNA from nonsense-mediated decay.


亚细胞位置:
Nucleus Endoplasmic reticulum Cytoplasm Predominantly nuclear where it localizes to heterochromatin. Also cytoplasmic where it is found at the outer surface of the endoplasmic reticulum (By similarity). Shuttles between the nucleus and cytoplasm. May be transported into the nucleus by the nuclear import protein TNPO2/TRN2 or by APOBEC1.


该产品尚未在任何出版物中被引用。

[1].
"The apolipoprotein B mRNA editing complex performs a multifunctional cycle and suppresses nonsense-mediated decay."

[2].
"A novel nuclear localization signal in the auxiliary domain of apobec-1 complementation factor regulates nucleocytoplasmic import and shuttling."

[3].
"Two proteins essential for apolipoprotein B mRNA editing are expressed from a single gene through alternative splicing."

[4].
"Identification of domains in apobec-1 complementation factor required for RNA binding and apolipoprotein-B mRNA editing."

[5].
"Isolation, characterization and developmental regulation of the human apobec-1 complementation factor (ACF) gene."

[6].
"Molecular cloning of apobec-1 complementation factor, a novel RNA-binding protein involved in the editing of apolipoprotein B mRNA."

[7].
"Targeted deletion of the murine apobec-1 complementation factor (acf) gene results in embryonic lethality."

[8].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[9].
"The DNA sequence and comparative analysis of human chromosome 10."

[10].
"Identification of GRY-RBP as an apolipoprotein B RNA-binding protein that interacts with both apobec-1 and apobec-1 complementation factor to modulate C to U editing."
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