85-6260-55　LYAG Rabbit Polyclonal Antibody 50ul　BT-AP03502

特徴

• 背景：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.

仕様

• サイズ：50ul
• 抗原：Synthesized peptide derived from human LYAG
• 免疫動物：Rabbit
• 交差性：Human, Mouse, Rat
• 適用：WB
• クラス：IgG
• クロナリティ：Polyclonal
• 濃度：1 mg/ml
• 別名：LYAG; Lysosomal alpha-glucosidase; EC 3.2.1.20; Acid maltase; Aglucosidase alfa; 76 kDa lysosomal alpha-glucosidase; 70 kDa lysosomal alpha-glucosidase;
• この商品は法規制を確認しておりません。（法規制によって販売できない場合もございます）

• 【試薬に関するお問合せ】
• アズワン株式会社 試薬・プロセス材料グループ
• TEL：06-6447-8641
• FAX：06-6447-8642
• E-mail：[email protected]