ELISA試劑盒

PCR試劑盒

生化試劑盒

農(nóng)殘檢測(cè)試劑盒

細(xì)胞庫(kù)

基礎(chǔ)培養(yǎng)基

完全培養(yǎng)基

原代細(xì)胞

細(xì)胞專用培養(yǎng)基

細(xì)胞系

菌株

生化試劑

病理染色液

科研抗體

形態(tài)病理檢測(cè)

GM2A抗原（重組蛋白）

規(guī)格：

價(jià)格：￥

品牌 : 通蔚生物
目錄號(hào) : TW11238
應(yīng)用 : 僅供科研使用
貨期 : 現(xiàn)貨
規(guī)格：1mg/100ug

中文名稱：GM2A 抗原（重組蛋白）

英文名稱：GM2A Antigen (Recombinant Protein)

別名：GM2 ganglioside activator; SAP-3; GM2-AP

相關(guān)類別：抗原

儲(chǔ) 存：冷凍（-20℃）

概述

Fusion protein corresponding to a region derived from 34-193 amino acids of human GM2A

技術(shù)規(guī)格

Full name:

GM2 ganglioside activator

Synonyms:

SAP-3; GM2-AP

Swissprot:

P17900

Gene Accession:

BC009273

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 small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.

021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

農(nóng)殘檢測(cè)試劑盒

細(xì)胞庫(kù)

基礎(chǔ)培養(yǎng)基

完全培養(yǎng)基

原代細(xì)胞

細(xì)胞專用培養(yǎng)基

細(xì)胞系

菌株

生化試劑

病理染色液

科研抗體

標(biāo)準(zhǔn)品

血清

形態(tài)病理檢測(cè)

分子病理

超微病理

細(xì)胞凋亡與檢測(cè)

產(chǎn)品中心

最新產(chǎn)品

相關(guān)文章

GM2A抗原（重組蛋白）

Full name:	GM2 ganglioside activator
Synonyms:	SAP-3; GM2-AP
Swissprot:	P17900
Gene Accession:	BC009273
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 small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.