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Pgap3 (基因名), Post-GPI attachment to proteins factor 3 (蛋白名), PGAP3_MOUSE.
产品名称:

Mouse Pgap3/ Post-GPI attachment to proteins factor 3 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 Pgap3 Peptide
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Mouse Pgap3 Peptide
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R&D 技术数据
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该产品尚未在任何出版物中被引用。

[1].
"PER1 is required for GPI-phospholipase A2 activity and involved in lipid remodeling of GPI-anchored proteins."

[2].
"MGC9753 gene, located within PPP1R1B-STARD3-ERBB2-GRB7 amplicon on human chromosome 17q12, encodes the seven-transmembrane receptor with extracellular six-cystein domain."

[3].
"Identification of the CAB2/hCOS16 gene required for the repair of DNA double-strand breaks on a core amplified region of the 17q12 locus in breast and gastric cancers."

[4].
"Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation."

[5].
"Fatty acid remodeling of GPI-anchored proteins is required for their raft association."

[6].
"HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer."

[7].
"Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries."

[8].
"Evolutionary recombination hotspot around GSDML-GSDM locus is closely linked to the oncogenomic recombination hotspot around the PPP1R1B-ERBB2-GRB7 amplicon."

[9].
"The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment."

[10].
"PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation."
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