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XPNPEP2 Anticuerpo, Mabs de conejo

  • XPNPEP2 Antibody, Rabbit MAb, Immunohistochemistry
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Humano XPNPEP2 Información de producto de anticuerpo
Inmunogen:Recombinant Human XPNPEP2 protein (Catalog#11903-H08H)
Clone ID:020
Tipo de Ig:Rabbit IgG
Concentración:
Endotoxina:
Formulación:0.2 μm filtered solution in PBS with 5% trehalose
Preparación:This antibody was obtained from a rabbit immunized with purified, recombinant Human XPNPEP2 (rh XPNPEP2; Catalog#11903-H08H; O43895; Met1-Ala650).
Humano XPNPEP2 Guía de uso de anticuerpo
Especificidad:Human XPNPEP2
Aplicación:IHC-P

IHC-P: 1-10 μg/mL

Almacenamiento:
Humano XPNPEP2 Antibody IHC Application Image
XPNPEP2 Antibody, Rabbit MAb, Immunohistochemistry
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Caption:
Immunochemical staining of human XPNPEP2 in human kidney with rabbit monoclonal antibody (10 µg/mL, formalin-fixed paraffin embedded sections).
Other XPNPEP2 Antibody Products
XPNPEP2 Fondo

Aminopeptidase P (APP) is a hydrolase specific for N-terminal imido bonds, which are common to several collagen degradation products, neuropeptides, vasoactive peptides, and cytokines. A membrane-bound and soluble form of this enzyme (XPNPEP2) have been identified as products of two separate genes. XPNPEP2, the X-linked gene that encodes membranous aminopeptidase P (APP), has been reported to associate with APP activity. The membrane aminopeptidase P (XPNPEP2) is largely limited in distribution to endothelia and brush border epithelia. APP and XPNPEP2 contain homologous blocks of sequence common to members of the "pita bread-fold" protein family, of which Escherichia coli methionine aminopeptidase is the prototype. The C-2399A variant in XPNPEP2 is associated with reduced APP activity and a higher incidence of AE-ACEi. XPNPEP2 mRNA was detected in fibroblasts that carry the translocation, suggesting that this gene at least partially escapes X inactivation. XPNPEP2 is a candidate gene for premature ovarian failure (POF).

Humano XPNPEP2 Referencias
  • Sprinkle TJ, et al. (2000) Cloning, chromosomal sublocalization of the human soluble aminopeptidase P gene (XPNPEP1) to 10q25.3 and conservation of the putative proton shuttle and metal ligand binding sites with XPNPEP2. Arch Biochem Biophys. 378(1): 51-6.
  • Prueitt RL, et al. (2000) Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene. Cytogenet Cell Genet. 89(1-2): 44-50.
  • Duan QL, et al. (2005) A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors. Am J Hum Genet. 77(4): 617-26.
  • Woodard-Grice AV, et al. (2010) Sex-dependent and race-dependent association of XPNPEP2 C-2399A polymorphism with angiotensin-converting enzyme inhibitor-associated angioedema. Pharmacogenet Genomics. 20(9): 532-6.
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    Size / Price
    Catálogo: 11903-R020-50
    Precio de lista: 
    Precio:      (You Save: )
    Tamaño:
    50 µg
    100 µg
    Cantidad:+-
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    Datasheet & Documentation

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