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Nt5c3a (基因名), Cytosolic 5'-nucleotidase 3A (蛋白名), 5NT3A_MOUSE.
产品名称:

Mouse Nt5c3a/ Cytosolic 5'-nucleotidase 3A Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

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

来源:
E.coli
种属:
Mouse
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.
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:
-
Mouse Nt5c3a Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


通用注释


Sub Unit:
Monomer.


Function:
Nucleotidase which shows specific activity towards cytidine monophosphate (CMP) and 7-methylguanosine monophosphate (m(7)GMP). CMP seems to be the preferred substrate.


Subcellular Location:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Human erythrocyte pyrimidine 5-nucleotidase, PN-I, is identical to p36, a protein associated to lupus inclusion formation in response to alpha-interferon."

[2].
"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."

[3].
"Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemia."

[4].
"Molecular characterization of six unrelated Italian patients affected by pyrimidine 5'-nucleotidase deficiency."

[5].
"Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency."

[6].
"Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells."

[7].
"Purification, microsequencing, and immunolocalization of p36, a new interferon-alpha-induced protein that is associated with human lupus inclusions."

[8].
"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."

[9].
"Cytosolic 5'-nucleotidase III (NT5C3): gene sequence variation and functional genomics."

[10].
"Evidence for essential catalytic determinants for human erythrocyte pyrimidine 5'-nucleotidase."
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