FITC标记的磷脂酸磷酸酶LPIN2抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的磷脂酸磷酸酶LPIN2抗体

FITC标记的磷脂酸磷酸酶LPIN2抗体

商家询价

产品名称: FITC标记的磷脂酸磷酸酶LPIN2抗体

英文名称: Anti-Lipin 2/FITC

产品编号: HZ-18290R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

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 Rabbit Anti-Lipin 2/FITC Conjugated antibody

FITC标记的磷脂酸磷酸酶LPIN2抗体

 

英文名称 Anti-Lipin 2/FITC
中文名称 FITC标记的磷脂酸磷酸酶LPIN2抗体
别    名 KIAA0249; Lipin-2; Lipin2; LPIN 2; LPIN2; LPIN2_HUMAN; OTTHUMP00000162242; Phosphatidate phosphatase LPIN2.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  免疫学  激酶和磷酸酶  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 99kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Lipin 2
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
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]

Function:
Plays important roles in controlling the metabolism of fatty acids at differents levels. Acts as a magnesium-dependent phosphatidate phosphatase enzyme which catalyzes the conversion of phosphatidic acid to diacylglycerol during triglyceride, phosphatidylcholine and phosphatidylethanolamine biosynthesis in the reticulum endoplasmic membrane. Acts also as a nuclear transcriptional coactivator for PPARGC1A to modulate lipid metabolism.

Subcellular Location:
Nucleus. Cytoplasm > cytosol. Endoplasmic reticulum membrane. Translocates to endoplasmic reticulum membrane with increasing levels of oleate.

Tissue Specificity:
Expressed in liver, lung, kidney, placenta, spleen, thymus, lymph node, prostate, testes, small intestine, and colon.

DISEASE:
Defects in LPIN2 are the cause of Majeed syndrome (MAJEEDS) [MIM:609628]. An autosomal recessive syndrome characterized by chronic recurrent multifocal osteomyelitis that is of early onset with a lifelong course, congenital dyserythropoietic anemia that presents as hypochromic, microcytic anemia during the first year of life and ranges from mild to transfusion-dependent, and transient inflammatory dermatosis, often manifesting as Sweet syndrome (neutrophilic skin infiltration).

Similarity:
Belongs to the lipin family.

Database links:

Entrez Gene: 9663 Human

Entrez Gene: 64898 Mouse

Entrez Gene: 316737 Rat

Omim: 605519 Human

SwissProt: Q92539 Human

SwissProt: Q99PI5 Mouse

Unigene: 132342 Human

Unigene: 227924 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications
   

小鼠研究表明,该基因在正常脂肪组织发育过程中起作用,可能在人体甘油三酯代谢中发挥作用。该基因代表了人类脂肪营养不良的候选基因,特征是体脂肪丢失、脂肪肝、高甘油三酯血症和胰岛素抵抗。[ RefSeq,JUL 2008 ]