日日操日日操,亚洲日本午夜激情,人妻内射精品一区二区,国产一区北条麻妃

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
美女日逼视視,欧美熟女人妻a
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-LCAT/Gold Conjugated antibody (bs-1972R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-1972R-Gold
英文名稱 Rabbit Anti-LCAT/Gold Conjugated antibody
中文名稱 膠體金標記的卵磷酯膽固醇?;D移酶抗體
別    名 LCAT; LCAT_HUMAN; Lecithin cholesterol acyltransferase; Lecithin-cholesterol acyltransferase; Phosphatidylcholine sterol acyltransferase; Phosphatidylcholine-sterol acyltransferase; Phospholipid cholesterol acyltransferase; Phospholipid-cholesterol acyltransferase.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  心血管  免疫學  神經(jīng)生物學  信號轉導  激酶和磷酸酶  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
產(chǎn)品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 47kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human LCAT
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
This gene encodes the extracellular cholesterol esterifying enzyme, lecithin-cholesterol acyltransferase. The esterification of cholesterol is required for cholesterol transport. Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency. [provided by RefSeq, Jul 2008]

Function:
Central enzyme in the extracellular metabolism of plasma lipoproteins. Synthesized mainly in the liver and secreted into plasma where it converts cholesterol and phosphatidylcholines (lecithins) to cholesteryl esters and lysophosphatidylcholines on the surface of high and low density lipoproteins (HDLs and LDLs). The cholesterol ester is then transported back to the liver. Has a preference for plasma 16:0-18:2 or 18:O-18:2 phosphatidylcholines. Also produced in the brain by primary astrocytes, and esterifies free cholesterol on nascent APOE-containing lipoproteins secreted from glia and influences cerebral spinal fluid (CSF) APOE- and APOA1 levels. Together with APOE and the cholesterol transporter ABCA1, plays a key role in the maturation of glial-derived, nascent lipoproteins. Required for remodeling high-density lipoprotein particles into their spherical forms.

Subcellular Location:
Secreted. Note=Secreted into blood plasma. Produced in astrocytes and secreted into cerebral spinal fluid (CSF).

Tissue Specificity:
Expressed mainly in brain, liver and testes. Secreted into plasma and cerebral spinal fluid. Expressed in Hep-G2 cell line.

Post-translational modifications:
O- and N-glycosylated. O-glycosylation on Thr-431 and Ser-433 consists of sialylated galactose beta 1-->3N-acetylgalactosamine structures. N-glycosylated sites contain sialylated triantennary and/or biantennary complex structures.

DISEASE:
Lecithin-cholesterol acyltransferase deficiency (LCATD) [MIM:245900]: A disorder of lipoprotein metabolism characterized by inadequate esterification of plasmatic cholesterol. Two clinical forms are recognized: complete LCAT deficiency and fish-eye disease. LCATD is generally referred to the complete form which is associated with absence of both alpha and beta LCAT activities resulting in esterification anomalies involving both HDL (alpha-LCAT activity) and LDL (beta-LCAT activity). It causes a typical triad of diffuse corneal opacities, target cell hemolytic anemia, and proteinuria with renal failure. Note=The disease is caused by mutations affecting the gene represented in this entry.
Fish-eye disease (FED) [MIM:136120]: A disorder of lipoprotein metabolism due to partial lecithin-cholesterol acyltransferase deficiency that affects only alpha-LCAT activity. FED is characterized by low plasma HDL and corneal opacities due to accumulation of cholesterol deposits in the cornea ('fish-eye'). Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the AB hydrolase superfamily. Lipase family.

Database links:

Entrez Gene: 3931 Human

Entrez Gene: 16816 Mouse

Entrez Gene: 24530 Rat

Omim: 606967 Human

SwissProt: P04180 Human

SwissProt: P16301 Mouse

SwissProt: P18424 Rat

Unigene: 387239 Human

Unigene: 1593 Mouse

Unigene: 10481 Rat



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

LCAT是參與體內(nèi)脂質代謝的主要成份之一,是一種在高密度脂蛋白(HDL)代謝和動脈粥樣硬化(AS)發(fā)展中的關鍵酶。LCAT需要經(jīng)載脂蛋白ApoAI、載脂蛋白D(ApoD)作為輔助因子并經(jīng)ApoE活化來發(fā)揮作用。
版權所有 2004-2026 m.bklrv.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網(wǎng)安備110107000727號
久久的一级黄色片| 大香蕉大香蕉最新视频| 国产3P在线播放| 91japanesefree国产| 国产性五月| 欧美日韩一区五月天| 人妻人人人| 熟女精品成人| 久久久999不卡| 411精品中出一区二区| 嫩草aV无码| 亚洲AV午夜精品一二三| 国产激情天天干| 黑水县| 久久高清免费AV| 日本欧美久久精品免费| 欧美日韩高清久久| 日韩日韩和欧美一区二区| 欧美激情综合一区| 亚洲在线 porn| 97无码精品人妻一区二区下载| 这里只有精品 在线| 大黑屌好舒服啊| 亚洲v国产v| 国产一二区麻豆东北| 日韩精品一极二极久久久久久久| 国产精品干bb视频| 啊啊啊嗯嗯嗯嗯嗯网址| 日本久热中文字幕精品| 阿根廷人妻无码专区| 天天爽日日爽精品综合网| 亚洲动作av伦理小说在线观看| 宅男av影视| 字幕无码一区| 超碰在线免费 (C Porn| 97超碰一区二区| 美欧一二三区麻豆| 全球成人综合在线| 不卡区一区免费观看| 婷婷欧美国产一区| 亚洲成人久久肉肉|