XPNPEP1 recombinant monoclonal antibody, clone SAIC-07E-1
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Specification
Product Description
Rabbit recombinant monoclonal antibody raised against synthetic peptide corresponding to peptide "TLSLDEVYLIDSGAQYK" derived from Xaa-Pro aminopeptidase 1 conjugated to KLH.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against recombinant protein corresponding to peptide "TLSLDEVYLIDSGAQYK" derived from Xaa-Pro aminopeptidase 1 conjugated to KLH.
Sequence
TLSLDEVYLIDSGAQYK
Reactivity
Human
Form
Liquid
Isotype
IgG kappa
Recommend Usage
ELISA
Flow cytometry
Immunofluorescence
Immuno-MRM
Western Blot
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.02% Proclin 300)
Storage Instruction
Store at 4°C for 3 months. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing. -
Applications
Western Blot
Western blot analysis of HeLa, Jurkat, MCF7, HepG2, A549, HEK293 cell lysates using anti-XPNPEP1 recombinant monoclonal antibody, clone SAIC-07E-1 (Cat # RAB03971).Immunofluorescence
Immunofluorescence analysis of XPNPEP1 (green) in HeLa cells using human anti-XPNPEP1 recombinant monoclonal antibody, clone SAIC-07E-1 (Cat # RAB03971), and DAPI(blue).Enzyme-linked Immunoabsorbent Assay
Flow Cytometry
Flow-cytometry analysis of XPNPEP1 in HeLa cells using human anti-XPNPEP1 recombinant monoclonal antibody, clone SAIC-07E-1 (Cat # RAB03971).Immuno-MRM (multiple reaction monitoring)
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Gene Info — XPNPEP1
Entrez GeneID
7511Protein Accession#
Q9NQW7Gene Name
XPNPEP1
Gene Alias
SAMP, XPNPEP, XPNPEPL, XPNPEPL1
Gene Description
X-prolyl aminopeptidase (aminopeptidase P) 1, soluble
Omim ID
602443Gene Ontology
HyperlinkGene Summary
X-prolyl aminopeptidase (EC 3.4.11.9) is a proline-specific metalloaminopeptidase that specifically catalyzes the removal of any unsubstituted N-terminal amino acid that is adjacent to a penultimate proline residue. Because of its specificity toward proline, it has been suggested that X-prolyl aminopeptidase is important in the maturation and degradation of peptide hormones, neuropeptides, and tachykinins, as well as in the digestion of otherwise resistant dietary protein fragments, thereby complementing the pancreatic peptidases. Deficiency of X-prolyl aminopeptidase results in excretion of large amounts of imino-oligopeptides in urine (Blau et al., 1988 [PubMed 3141711]).[supplied by OMIM
Other Designations
OTTHUMP00000020457|OTTHUMP00000058856|X-prolyl aminopeptidase (aminopeptidase P) 1, soluble (SAMP, XPNPEP, XPNPEPL)|X-prolyl aminopeptidase (aminopeptidase P)-like
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Interactome
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Disease
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