产品货号：
JN1754
中文名称：
重组人XPNPEP3
英文名称：
Recombinant Human Probable Xaa-Pro Aminopeptidase 3
产品规格：
10μg|50μg|500μg|1mg
发货周期：
1～3天
产品价格：
询价
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Ser507在N端、C端都带有His标签。
XPNPEP3质量控制：＞95%(还原性SDS-PAGE)
XPNPEP3制剂：液体
XPNPEP3保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于XPNPEP3：
Probable Xaa-Pro Aminopeptidase 3 (XPNPEP3) is a member of the peptidase M24B family. XPNPEP3 has two isoforms and both are widely expressed. XPNPEP3 is localized in the Mitochondrion. XPNPEP3 catalyzes the release of any N-terminal amino acid, including proline, that is linked to proline, even from a dipeptide or tripeptide. Defects in XPNPEP3 are the cause of nephronophthisis-like nephropathy type 1 which is a disorder with features of nephronophthisis, a cystic kidney disease leading to end-stage renal failure.
相关搜索：重组人XPNPEP3
XPNPEP3质量控制：＞95%(还原性SDS-PAGE)
XPNPEP3制剂：液体
XPNPEP3保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于XPNPEP3：
Probable Xaa-Pro Aminopeptidase 3 (XPNPEP3) is a member of the peptidase M24B family. XPNPEP3 has two isoforms and both are widely expressed. XPNPEP3 is localized in the Mitochondrion. XPNPEP3 catalyzes the release of any N-terminal amino acid, including proline, that is linked to proline, even from a dipeptide or tripeptide. Defects in XPNPEP3 are the cause of nephronophthisis-like nephropathy type 1 which is a disorder with features of nephronophthisis, a cystic kidney disease leading to end-stage renal failure.
相关搜索：重组人XPNPEP3