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FITC標(biāo)記的溶(róng)血磷脂酸(suān)酰(xiān)基轉移酶β抗體(tǐ)

文字(zì):[大][中(zhōng)][小(xiǎo)] 2017-5-3    瀏(liú)覽(lǎn)次數:1510    

                                   FITC標記的溶血磷脂酸(suān)酰(xiān)基(jī)轉(zhuǎn)移酶β抗(kàng)體(tǐ)                                                                                                                                                
英(yīng)文名稱(chēng)Anti-Agpat2/FITC
中文(wén)名稱(chēng):FITC標記(jì)的(dí)溶(róng)血(xiě)磷(lín)脂(zhī)酸酰基轉(zhuǎn)移(yí)酶β抗體(tǐ)
別    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 AGP acyltransferase 2; 1 AGPAT2 antibody Berardinelli Seip congenital lipodystrophy.PLCB_HUMAN  

詳(xiáng)細(xì)介紹:


規格:100ul 
說(shuō) 明(míng) 書(shū)100ul  
研究領域腫瘤(liú)  細胞生(shēng)物  免疫(yì)學(xué)  轉錄(lù)調(tiáo)節因子  
抗(kàng)體(tǐ)來源Rabbit
克隆(lóng)類型(xíng)Polyclonal
交(jiāo)叉反應 Human, Mouse, Rat, Dog, Pig, Cow, Horse, 
產品應(yīng)用IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子(zǐ) 量(liáng)30kDa
細(xì)胞(bāo)定(dìng)位細(xì)胞膜 
性(xìng)    狀(zhuàng)Lyophilized or Liquid
濃    度(dù)1mg/ml
免 疫 原(yuán)KLH conjugated synthetic peptide derived from human LPAAB
亞(yà)    型IgG
純化(huà)方(fāng)法affinity purified by Protein A
儲 存(cún) 液(yè)0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保(bǎo)存(cún)條件(jiàn)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.

相關資料(liào):


產(chǎn)品介紹(shào)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.

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