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LPIN2 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN2338
产品名称
LPIN2 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
LPIN2 KIAA0249
蛋白名称
Phosphatidate phosphatase LPIN2 (EC 3.1.3.4) (Lipin-2)
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
9663
Human Swissprot No.
Q92539
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q92539/entry
Mouse Swissprot No.
Q99PI5
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q99PI5
免疫原
Synthesized peptide derived from human protein . at AA range: 220-300
特异性
LPIN2 Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500-2000 ELISA 1:5000-20000
预测分子量
98kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
Mouse studies suggest that this gene functions during normal adipose tissue development and may play a role in human triglyceride metabolism. This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. [provided by RefSeq, Jul 2008],
组织表达
Expressed in liver, lung, kidney, placenta, spleen, thymus, lymph node, prostate, testes, small intestine, and colon.
细胞定位
Nucleus . Cytoplasm, cytosol . Endoplasmic reticulum membrane . Translocates to endoplasmic reticulum membrane with increasing levels of oleate. .
功能
disease:Defects in LPIN2 are the cause of Majeed syndrome [MIM:609628]. Majeed syndrome is an autosomal recessive disorder combining features of chronic recurrent multifocal osteomyelitis [MIM:259680], congenital dyserythropoietic anemia and inflammatory dermatosis.,online information:Repertory of FMF and hereditary autoinflammatory disorders mutations,similarity:Belongs to the lipin family.,tissue specificity:Expressed in liver, lung, kidney, placenta, spleen, thymus, lymph node, prostate, testes, small intestine, and colon.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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