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AGPAT2 (基因名), 1-acyl-sn-glycerol-3-phosphate acyltransferase beta (蛋白名), PLCB_HUMAN.
产品名称:

Human AGPAT2/ 1-acyl-sn-glycerol-3-phosphate acyltransferase beta Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Human
序列:
预估分子量:
31kDa (monomer)
应用:
WB
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human AGPAT2 Peptide
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Human AGPAT2 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].
"Cloning and expression of two human lysophosphatidic acid acyltransferase cDNAs that enhance cytokine-induced signaling responses in cells."

[2].
"Enzymatic activity of naturally occurring 1-acylglycerol-3-phosphate-O-acyltransferase 2 mutants associated with congenital generalized lipodystrophy."

[3].
"AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34."

[4].
"Human lysophosphatidic acid acyltransferase. cDNA cloning, expression, and localization to chromosome 9q34.3."

[5].
"Human 1-acylglycerol-3-phosphate O-acyltransferase isoforms 1 and 2: biochemical characterization and inability to rescue hepatic steatosis in Agpat2(-/-) gene lipodystrophic mice."

[6].
"Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome."

[7].
"Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy."

[8].
"Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instability."

[9].
"Talon cusps, macrodontia, and aberrant tooth morphology in Berardinelli-Seip syndrome."

[10].
"Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients."
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