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GAA Rabbit pAb
货号: DPA03046
GAA Rabbit pAb
反应种属:
HumanMouseRat
应用:
WB
¥ 960
/ 50μl
库存充足
50μl100μl
产品详情
推荐稀释比
产品特性
反应种属
HumanMouseRat
应用
WB
纯化方式
Affinity Purification
免疫源
A synthetic peptide of human GAA
来源
Rabbit
克隆性
Polyclonal
Background
This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
预测分子量
105 kDa
GeneID
2548
Uniprot
P10253
Isotype
IgG
分子量
76 kDa
标记类型
Un-conjugated
产品别名
LYAG
货号: DPA03046
GAA Rabbit pAb
反应种属:
HumanMouseRat
应用:
WB
¥ 960
/ 50μl
库存充足
50μl100μl
产品详情
推荐稀释比
产品特性
反应种属
HumanMouseRat
应用
WB
纯化方式
Affinity Purification
免疫源
A synthetic peptide of human GAA
来源
Rabbit
克隆性
Polyclonal
Background
This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
预测分子量
105 kDa
GeneID
2548
Uniprot
P10253
Isotype
IgG
分子量
76 kDa
标记类型
Un-conjugated
产品别名
LYAG
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