中文名稱： FUS 抗原（重組蛋白）

英文名稱： FUS Antigen (Recombinant Protein)

別名：FUS RNA binding protein; TLS; ALS6; ETM4; FUS1; POMP75; HNRNPP2

儲存：冷凍（-20℃）

相關(guān)類別：抗原

概述

Fusion protein corresponding to C terminal 77 amino acids of human FUS

技術(shù)規(guī)格

Full name:

FUS RNA binding protein

Synonyms:

TLS; ALS6; ETM4; FUS1; POMP75; HNRNPP2

Swissprot:

P35637

Gene Accession:

BC000402

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6.

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FUS 抗原（重組蛋白）說明書
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021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

細胞系

細胞庫

基礎(chǔ)培養(yǎng)基

完全培養(yǎng)基

原代細胞

細胞專用培養(yǎng)基

菌株

生化試劑

病理染色液

科研抗體

標準品

血清

形態(tài)病理檢測

分子病理

超微病理

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FUS 抗原（重組蛋白）

Full name:	FUS RNA binding protein
Synonyms:	TLS; ALS6; ETM4; FUS1; POMP75; HNRNPP2
Swissprot:	P35637
Gene Accession:	BC000402
Purity:	>85%, as determined by Coomassie blue stained SDS-PAGE
Expression system:	Escherichia coli
Tags:	His tag C-Terminus, GST tag N-Terminus
Background:	This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6.