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产品名称: 溶血磷脂酸?;泼甫驴固?/span>
产品型号: Agpat2
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

溶血磷脂酸?;泼甫驴固逵τ糜贗HC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。溶血磷脂酸酰基转移酶β抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


溶血磷脂酸?;泼甫驴固?/strong>  的详细介绍

溶血磷脂酸?;泼甫驴固?/strong>

规格:1mg/1ml

英文名: Agpat2

别名: LPAAB; BSCL; BSCL1; EC 2.3.1.51; LPAAB; LPAAT beta; Lysophosphatidic acid acyltransferase beta; 1 acyl sn glycerol 3 phosphate acyltransferase beta; 1 acylglycerol 3 phosphate O acyltransferase 2; 1 A

分子量: 30kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

溶血磷脂酸?;泼甫驴固?/strong>**原:KLH conjugated synthetic peptide derived from human LPAAB

交叉反应:Human, Mouse, Rat, Dog, Pig, Cow, Horse,

细胞定位:细胞膜

产品介绍:background: Agpat2 is a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. It is located within the endoplasmic reticulum membrane and converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. Mutations in its have been associated with congenital generalized lipodystrophy (CGL), or Berardinelli-Seip syndrome, a disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. Function: Converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone. Subcellular Location: Membrane; Multi-pass membrane protein Tissue Specificity: Expressed predominantly in heart and溶血磷脂酸酰基转移酶β抗体 liver. DISEASE: Defects in AGPAT2 are the cause of congenital generalized lipodystrophy type 1 (CGL1) [MIM:608594]; also known as Berardinelli-Seip congenital lipodystrophy type 1 (BSCL1) or Berardinelli-Seip syndrome. CGL1 is an autosomal recessive disorder characterized by marked paucity of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of溶血磷脂酸?;泼甫驴固?/strong> diabetes. Similarity: Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family. Gene ID: 10555 Database links: Entrez Gene: 10555 Human Entrez Gene: 67512 Mouse Entrez Gene: 311821 Rat Omim: 603100 Human SwissProt: O15120 Human SwissProt: Q8K3K7 Mouse Unigene: 320151 Human Unigene: 24244 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

溶血磷脂酸?;泼甫驴固?/strong>产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:肿瘤  细胞生物  **学  转录调节因子  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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