GAA (Human) Recombinant Protein (Q01)
产品名称： GAA (Human) Recombinant Protein (Q01)
英文名称： GAA (Human) Recombinant Protein (Q01)
产品编号： H00002548-Q01
产品价格： 0
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围： null
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
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- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Human GAA partial ORF ( AAH40431, 851 a.a. - 952 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- GEARGELFWDDGESLEVLERGAYTQVIFLARNNTIVNELVRVTSEGAGLQLQKVTVLGVATAPQQVLSNGVPVSNFTYSPDTKVLDICVSLLMGEQFLVSWC
- Theoretical MW (kDa):
- 36.96
- Preparation Method:
- in vitro wheat germ expression system
- Purification:
- Glutathione Sepharose 4 Fast Flow
- Storage Buffer:
- 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
- Storage Instruction:
- Store at -80°C. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- 12.5% SDS-PAGE Stained with Coomassie Blue.
- Note:
- Best use within three months from the date of receipt of this protein.
- MSDS:
Download
- Application Image
- Enzyme-linked Immunoabsorbent Assay
- Western Blot (Recombinant protein)
- Antibody Production
- Protein Array
- Entrez GeneID:
- 2548
- GeneBank Accession#:
- BC040431
- Protein Accession#:
- AAH40431
- Gene Name:
- GAA
- Gene Alias:
- LYAG
- Gene Description:
- glucosidase, alpha; acid
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq
- Other Designations:
- acid alpha-glucosidase,acid maltase,alpha-glucosidase,glycogen storage disease type II,lysosomal alpha-glucosidase