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  • ALS2 抗原(重組蛋白)

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    • 品牌 : 通蔚生物
    • 目錄號(hào) : TW15887
    • 應(yīng)用 : 僅限于科研使用
    • 保存條件 : 低溫保存
    • 貨期 : 現(xiàn)貨
    • 商品庫(kù)存:90
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中文名稱:ALS2 抗原(重組蛋白)

英文名稱: ALS2 Antigen (Recombinant Protein)

別      名: amyotrophic lateral sclerosis 2 (juvenile); ALSJ; PLSJ; IAHSP; ALS2CR6

儲(chǔ)      存: 冷凍(-20℃)

相關(guān)類別: 抗原

概  述:

Fusion protein corresponding to C terminal 250 amino acids of human ALS2

   
技術(shù)規(guī)格:

Full name:

amyotrophic lateral sclerosis 2 (juvenile)

Synonyms:

ALSJ; PLSJ; IAHSP; ALS2CR6

Swissprot:

Q96Q42

Gene Accession:

BC029174

Purity:

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

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene.