Nt5c3a (GeneName), Cytosolic 5'-nucleotidase 3A (ProteinName), 5NT3A_MOUSE.
Mouse Nt5c3a/ Cytosolic 5'-nucleotidase 3A ELISA Kit
7-methylguanosine phosphate-specific 5'-nucleotidase, 7-methylguanosine nucleotidase, Cytosolic 5'-nucleotidase 3, Cytosolic 5'-nucleotidase III, cN-III, Lupin, Pyrimidine 5'-nucleotidase 1, P5'N-1, Nt5c3
Natural and recombinant mouse Cytosolic 5'-nucleotidase 3A
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Nucleotidase which shows specific activity towards cytidine monophosphate (CMP) and 7-methylguanosine monophosphate (m(7)GMP). CMP seems to be the preferred substrate.
MDRAAVARVG | AVASASVCAV | VAGVVLAQYI | FTLKRKTGRK | TKIIEMMPEF |
QKSSVRIKNP | TRVEEIICGL | IKGGAAKLQI | ITDFDMTLSR | FSYNGKRCPT |
CHNIIDNCKL | VTDECRRKLL | QLKEQYYAIE | VDPVLTVEEK | FPYMVEWYTK |
SHGLLIEQGI | PKAKLKEIVA | DSDVMLKEGY | ENFFGKLQQH | GIPVFIFSAG |
IGDVLEEVIR | QAGVYHSNVK | VVSNFMDFDE | NGVLKGFKGE | LIHVFNKHDG |
ALKNTDYFSQ | LKDNSNIILL | GDSQGDLRMA | DGVANVEHIL | KIGYLNDRVD |
ELLEKYMDSY | DIVLVKEESL | EVVNSILQKT | L
This product has not yet been referenced specifically in any publications.
"Human erythrocyte pyrimidine 5-nucleotidase, PN-I, is identical to p36, a protein associated to lupus inclusion formation in response to alpha-interferon."
"Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutations."
"Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemia."
"Molecular characterization of six unrelated Italian patients affected by pyrimidine 5'-nucleotidase deficiency."
"Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency."
"Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells."
"Purification, microsequencing, and immunolocalization of p36, a new interferon-alpha-induced protein that is associated with human lupus inclusions."
"Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression."
"Cytosolic 5'-nucleotidase III (NT5C3): gene sequence variation and functional genomics."
"Evidence for essential catalytic determinants for human erythrocyte pyrimidine 5'-nucleotidase."
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