亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  聯系我們
菠萝蜜视频在线观看,无码a级毛片日韩精品,成人毛片一区二区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ETFA/APC Conjugated antibody (bs-0494R-APC)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-0494R-APC
英文名稱 Rabbit Anti-ETFA/APC Conjugated antibody
中文名稱 APC標記的電子轉移黃素蛋白α抗體
別    名 ETF-alpha; Electron transfer flavoprotein subunit alpha; electron-transfer-flavoprotein, alpha polypeptide; mitochondrial; Alpha ETF; Alpha-ETF; Electron transfer flavoprotein alpha polypeptide; Electron transfer flavoprotein alpha subunit; Electron transfer flavoprotein subunit alpha; Electron transfer flavoprotein subunit alpha mitochondrial; Electron transfer flavoprotein subunit alpha, mitochondrial; Electron transferring flavoprotein alpha polypeptide; EMA; ETFA; ETFA_HUMAN; GA2.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  信號轉導  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, Xenopuslaevis)
產品應用 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 37kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ETFA
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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.
產品介紹 background:
ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

Function:
The electron transfer flavoprotein serves as a specific electron acceptor for several dehydrogenases, including five acyl-CoA dehydrogenases, glutaryl-CoA and sarcosine dehydrogenase. It transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase).

Subunit:
Heterodimer of an alpha and a beta subunit.

Subcellular Location:
Mitochondrion matrix.

Post-translational modifications:
The N-terminus is blocked

DISEASE:
Defects in ETFA are the cause of glutaric aciduria type 2A (GA2A) [MIM:231680]; also known as glutaricaciduria IIA. GA2A is an autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It is characterized by multiple acyl-CoA dehydrogenase deficiencies resulting in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids.

Similarity:
Belongs to the ETF alpha-subunit/FixB family.

Database links:

Entrez Gene: 2108 Human

Entrez Gene: 110842 Mouse

Entrez Gene: 300726 Rat

Omim: 608053 Human

SwissProt: P13804 Human

SwissProt: Q99LC5 Mouse

SwissProt: P13803 Rat

Unigene: 39925 Human

Unigene: 290853 Mouse

Unigene: 32496 Rat



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

Involvement in disease:Defects in ETFA are the cause of glutaric aciduria type 2A (GA2A); also known as glutaricaciduria IIA. GA2A is an autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It is characterized by multiple acyl-CoA dehydrogenase deficiencies resulting in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids.
版權所有 2004-2026 www.www.chomd.com.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         京公網安備110107000727號
主站蜘蛛池模板: 色婷婷国产传媒综合久久| 亚洲中文久久精品无码|2020最新... | 日韩人妻无码一区二区三区久久99-久久. 日韩人 | 国产女主播在线视频| 中国护士18XXXXHD少妇| 色综合久久久久综合9999| 精品国产一二三产品价格新新影院| 香蕉久久综合深夜福利诱惑站| 亚洲精品老司机在线观看资源| 久久夜色精品国产噜噜亚洲SV|国产成人精品 | 99久久精品国产麻豆free| 无码乱人伦一区二区亚洲 - 无敌| 亚洲精品国产手机A| 无码国产精成人午夜96 | 四虎影视在线视频大全免费观看HD在线观看 | 中文人妻一区二区无码久久| 日本综合伊人色鬼久久| 成人H免费观看| 三上悠亚日韩精品一曲| 岛国不卡视频一区在线播放| 午夜精品一区二区三区免费视频刘涛激情大战 | 中文字幕综合亚洲国语对白| 男人的天堂无码动漫0V| 91偷拍一区二区三区精品| 日韩一区二区三区免费播放国| 丰满的奶水边做边喷白浆| 91久久国产综合久久91精品网站 | 亚洲中文字幕久久精品无码喷水是亚州最全的网站之一 | 亚洲综合国产成人丁香五月激情免费高清精品av| 三级毛片在线播放品善网| 99精品国产在热久久婷婷-久久婷婷五| 无码午夜福利片透明人系列| 国产成人无码18禁午夜福利网址木青| 岛国成人无码视频在现| 色婷婷777国产AMSR| 中文字幕一区二区三匹在线观看 | 人人模人人樉| 一区二区三区在线观看免费视频视频 | japanese在线播放jav 6park| 男人女人做爽爽视频国产91Prom| 中文字幕日韩高清无码4页|