Aspartylglucosaminidase/AGA Protein, Human, Recombinant (His)

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SPR兼容缓冲液

Aspartylglucosaminidase/AGA Protein, Human, Recombinant (His)

产品编号 TMPY-03972

AGA (Aspartylglucosaminidase) is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins. This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. Diseases associated with AGA include Aspartylglucosaminuria and Lysosomal Storage Disease. An important paralog of this gene is ASRGL1.

Aspartylglucosaminidase/AGA Protein, Human, Recombinant (His)

一键复制产品信息

SPR兼容缓冲液

产品编号 TMPY-03972

规格	价格	库存
5 μg	¥ 683	6-8日内发货
10 μg	¥ 1,130	6-8日内发货
20 μg	¥ 1,930	5日内发货
50 μg	¥ 4,430	5日内发货

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产品信息

生物活性	Measured by its ability to hydrolyze the AspAMC. The specific activity is >300 pmol/min/μg.
产品描述	AGA (Aspartylglucosaminidase) is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins. This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. Diseases associated with AGA include Aspartylglucosaminuria and Lysosomal Storage Disease. An important paralog of this gene is ASRGL1.
种属	Human
表达系统	HEK293 Cells
标签	C-His
蛋白编号	CAA39029.1
别名	GA,ASRG,aspartylglucosaminidase,AGU
蛋白构建	A DNA sequence encoding the human AGA (CAA39029.1) (Met1-Ile346) was expressed with a C-terminal polyhistidine tag. Predicted N terminal: Ser 24
蛋白纯度	> 95 % as determined by SDS-PAGE
分子量	36.1 kDa (predicted); 47, 29, 23 and 20 kDa (reducing condition, due to glycosylation)
内毒素	< 1.0 EU/μg of the protein as determined by the LAL method.
蛋白性状	Lyophilized powder
缓冲液	Lyophilized from a solution filtered through a 0.22 μm filter, containing PBS, pH 7.4. Typically, a mixture containing 5% to 8% trehalose, mannitol, and 0.01% Tween 80 is incorporated as a protective agent before lyophilization.
复溶方法	A Certificate of Analysis (CoA) containing reconstitution instructions is included with the products. Please refer to the CoA for detailed information.
存储	It is recommended to store recombinant proteins at -20°C to -80°C for future use. Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.
运输方式	In general, Lyophilized powders are shipping with blue ice.
研究背景	AGA (Aspartylglucosaminidase) is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins. This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. Diseases associated with AGA include Aspartylglucosaminuria and Lysosomal Storage Disease. An important paralog of this gene is ASRGL1.