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XPNPEP2 (基因名), Xaa-Pro aminopeptidase 2 (蛋白名), xpp2_human.
产品名称:

Human XPNPEP2/ Xaa-Pro aminopeptidase 2 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Aminoacylproline aminopeptidase, Membrane-bound aminopeptidase P, X-Pro aminopeptidase 2, Membrane-bound APP

序列号:
O43895
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Cell Biology
Human XPNPEP2 Protein
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Human XPNPEP2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


基因位点
Cytogenetic band: Xq26.1 by HGNC Xq26.1 by Entrez Gene Xq26.1 by Ensembl
XPNPEP2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Homotrimer.


功能:
Membrane-bound metalloprotease which catalyzes the removal of a penultimate prolyl residue from the N-termini of peptides, such as Arg-Pro-Pro. May play a role in the metabolism of the vasodilator bradykinin.


亚细胞位置:
Cell membrane Lipid-anchor GPI-anchor


该产品尚未在任何出版物中被引用。

[1].
"Cloning and tissue distribution of human membrane-bound aminopeptidase P."

[2].
"Sex-dependent and race-dependent association of XPNPEP2 C-2399A polymorphism with angiotensin-converting enzyme inhibitor-associated angioedema."

[3].
"A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors."

[4].
"Assignment of the membrane-bound human aminopeptidase P gene (XPNPEP2) to chromosome Xq25."

[5].
"A functional XPNPEP2 promoter haplotype leads to reduced plasma aminopeptidase P and increased risk of ACE inhibitor-induced angioedema."

[6].
"Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema."

[7].
"The DNA sequence of the human X chromosome."

[8].
"Human recombinant membrane-bound aminopeptidase P: production of a soluble form and characterization using novel, internally quenched fluorescent substrates."

[9].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[10].
"Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene."
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