吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
亚洲精品无码AV人在线观看国产,特级BBBBBBBBB视频,乱码丰满人妻一二三区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-SLC27A4/BF594 Conjugated antibody (bs-20458R-BF594)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-20458R-BF594
英文名稱1 Rabbit Anti-SLC27A4/BF594 Conjugated antibody
中文名稱 BF594標記的長鏈脂肪酸轉(zhuǎn)運蛋白4抗體
別    名 ACSVL 4; ACSVL-4; ACSVL4; EC 6.2.1; FATP 4; FATP4; Fatty acid transport protein 4; Fatty acid transport protein4; IPS; Long chain fatty acid transport protein 4; Long chain fatty acid transport protein4; OTTHUMP00000022264; S27A4; SLC27 A4; SLC27A 4; Solute carrier family 27 (fatty acid transporter) member 4; Solute carrier family 27 member 4; Solute carrier family 27 member4; S27A4_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 腫瘤  心血管  神經(jīng)生物學(xué)  信號轉(zhuǎn)導(dǎo)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse,  (predicted: Human, Rat, Pig, Rabbit, )
產(chǎn)品應(yīng)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 72kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SLC27A4
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(chǎn)品介紹 background:
This gene encodes a member of a family of fatty acid transport proteins, which are involved in translocation of long-chain fatty acids cross the plasma membrane. This protein is expressed at high levels on the apical side of mature enterocytes in the small intestine, and appears to be the principal fatty acid transporter in enterocytes. Clinical studies suggest this gene as a candidate gene for the insulin resistance syndrome. Mutations in this gene have been associated with ichthyosis prematurity syndrome. [provided by RefSeq, Apr 2010]

Function:
nvolved in translocation of long-chain fatty acids (LFCA) across the plasma membrane. Appears to be the principal fatty acid transporter in small intestinal enterocytes. Plays a role in the formation of the epidermal barrier. Required for fat absorption in early embryogenesis. Has acyl-CoA ligase activity for long-chain and very-long-chain fatty acids

Subcellular Location:
Membrane; Multi-pass membrane protein

Tissue Specificity:
Expressed at highest levels in brain, testis, colon and kidney. Expressed at medium levels in heart and liver, small intestine and stomach. Expressed at low levels in peripheral leukocytes, bone marrow, skeletal muscle and aorta. Expressed in adipose tissue.

DISEASE:
Defects in SLC27A4 are the cause of ichthyosis prematurity syndrome (IPS) [MIM:608649]. A keratinization disorder characterized by complications in the second trimester of pregnancy resulting from polyhydramnion, with premature birth of a child with thick caseous desquamating epidermis, respiratory complications and transient eosinophilia. After recovery during the first months of life, the symptoms are relatively benign and the patients suffer from a lifelong non-scaly ichthyosis with atopic manifestations.

Similarity:
Belongs to the ATP-dependent AMP-binding enzyme family.

Database links:

Entrez Gene: 10999 Human

Entrez Gene: 26569 Mouse

Omim: 604194 Human

SwissProt: Q6P1M0 Human

SwissProt: Q91VE0 Mouse

Unigene: 656699 Human

Unigene: 330113 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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
亚洲狠狠婷婷综合久久久久图片| 波多野结衣456| JAPANESEHD熟女熟妇伦| 亚洲AV无一区二区三区久久| 国产精品ⅴ无码大片在线看| 亚洲精品久久久久69影院 | 亚洲国产成人精品无码区在线观看 | 宝宝好涨水快流出来免费视频| 国产特级毛片AAAAAAA高清| 久久精品99国产精品日本| 拔萝卜视频免费观看高清下载| 日本工囗漫画H无遮挡全彩| 久久精品国产精品国产精品污| 人体内射精一区二区三区| 无码少妇高潮浪潮AV久久| 夜里十大禁用直播APP| 亚洲AV午夜国产精品无码中文字| 亚洲精品无码精品MV在线观看| 中文字幕一区二区三区日韩精品| 粉嫩XB粉嫩XB粉嫩XB| 中文乱码人妻系列一区二区| 天天爽夜夜爽人人爽| 被背叛的田川的忧郁| 国产成人A亚洲精V品无码| 国产一区二区三区| 色欲AV无码一区二区三区| 三级黄色视频| 伊人久久精品一区二区三区| 国产A国产片国产| 亚洲国产精品日韩AV不卡在线| 人妻少妇精品视频一区二区三区| av片在线观看免费| 国产精品99久久久久久WWW| 18禁网站| 亚洲AV无码精品色午夜果冻不卡 | 丰满少妇作爱视频免费观看| 国内精品国产成人国产三级| 女人被强╳到高潮喷水在线观看 | 亚洲熟女乱综合一区二区| 国产+日韩+另类+视频一区| 亚洲色无码A片一区二区麻豆|