脂滴包被蛋白础+叠抗体
规格：1尘驳/1尘濒
英文名： Perilipin A+B
别名： Lipid droplet associated protein; PERIA; PERIB; Perilipin A; Perilipin; Perilipin B; PerilipinA; PerilipinB; PLIN.
分子量： 54-56kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：笔辞濒测肠濒辞苍补濒
亚型：滨驳骋
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human Perilipi
交叉反应：Human, Mouse, Chicken, SheepDog,
细胞定位：细胞膜
脂滴包被蛋白础+叠抗体产物介绍：background: Perilipin is an intracellular neutral lipid droplet protein that is hormonally regulated. This protein is localized exclusively to the surface of lipid droplets. In response to lypotic stimuli, perilipin is phosphorylated by protein kinase A. Once activated, perilipin has inhibitory affects upon hormone-sensitive lipase (HSL), a protein that mediates the hydrolysis of triacylglycerol, the major form of stored energy in the body. Perilipin expression is limited to adipocytes and steroidogenic cells. There are currently two known isoforms, Perilipin A and B. Both of these proteins are encoded by a single-copy gene and are the result of differential splicing events. Function: Perilipin A: Modulator of adipocyte lipid metabolism. Coats lipid storage droplets to protect them from breakdown by hormone-sensitive lipase (HSL). Its absence may result in leanness. Perilipin B: May be involved in development and maintenance of adipose tissue. Subunit: Perilipin A: Interacts with ABHD5. Subcellular Location: Perilipin A: Lipid droplet. Note=Lipid droplet surface-associated. Perilipin B: Membrane; Peripheral membrane protein. Tissue 脂滴包被蛋白础+叠抗体Specificity: Perilipin A: Adipocytes. Perilipin B: Milk lipid globules. Post-translational modifications: Perilipin A: Major cAMP-dependent protein kinase-substrate in adipocytes, also dephosphorylated by PP1. When phosphorylated, may be maximally sensitive to HSL and when unphosphorylated, may play a role in the inhibition of lipolysis, by acting as a barrier in lipid droplet. Perilipin B: Acylated; primarily with C14, C16 and C18 fatty acids. DISEASE: Perilipin A: Defects in PLIN1 are the cause of familial partial lipodystrophy type 4 (FPLD4) [MIM:613877]. FPLD4 is a form of l脂滴包被蛋白础+叠抗体ipodystrophy characterized by loss of subcutaneous adipose tissue primarily affecting the lower limbs, insulin-resistant diabetes mellitus, hypertriglyceridemia, and hypertension. Perilipin B: Similarity: Perilipin A: Belongs to the perilipin family. Perilipin B: Belongs to the perilipin family. Gene ID: 5346 Database links: Entrez Gene: 5346 Human Entrez Gene: 103968 Mouse Entrez Gene: 25629 Rat Omim: 170290 Human SwissProt: O60240 Human SwissProt: Q8CGN5 Mouse SwissProt: P43884 Rat Unigene: 103253 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
脂滴包被蛋白础+叠抗体产物应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=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 心血管 细胞生物 信号转导
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid