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Pgap2 (基因名), Post-GPI attachment to proteins factor 2 (蛋白名), PGAP2_MOUSE.
产品名称:

Mouse Pgap2/ Post-GPI attachment to proteins factor 2 Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Mouse
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Mouse Pgap2 Peptide
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Mouse Pgap2 Peptide
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该产品尚未在任何出版物中被引用。

[1].
"Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability."

[2].
"Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer."

[3].
"PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome."

[4].
"PGAP2 is essential for correct processing and stable expression of GPI-anchored proteins."

[5].
"A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers."

[6].
"Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing."

[7].
"Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis--The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes."

[8].
"A human interactome in three quantitative dimensions organized by stoichiometries and abundances."

[9].
"A proteome-scale map of the human interactome network."

[10].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."
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