91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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  關(guān)于我們  聯(lián)系我們
嫩BBB槡BBBB槡BBBB电影,国产成人AV无码一区二区三区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-SLC27A4/PE-Cy5 Conjugated antibody (bs-20458R-PE-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-20458R-PE-Cy5
英文名稱 Rabbit Anti-SLC27A4/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5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.rvdoil.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
人人妻人人澡人人爽久久av | 欧美丰满少妇猛烈进入A片蜜桃 | 精品国产熟女AV | 亚洲精品成a人在线观看 | 午夜精品视频在线观看 | 日本在线观看免费 | 丰满岳乱妇毛片高清码成人 | 亚洲一二三中文字幕 | 无码人妻精品秘 入口 | A∨色狠狠一区二区三区 | 无码人妻精品一区二区蜜桃av | 无码人妻精品一区二区蜜桃漫画 | 欧美浓毛大BBB免费视频 | 少妇做爰免费视频播放 | 国产激情久久久久影院老熟女AV | 特大黑人巨交吊性XXXX视频 | 无码少妇一级A片在线观看 9l视频自拍蝌蚪9l成人 | 黄色视频免费在线观看 | 国产精品国产三级国产 | 超碰人人操人人干 | 亚洲日韩人妻中文字幕 | 狂揉小泬少妇精品无码 | 天天躁日日躁狠狠躁AV | 人妻少妇精品久久久久久久 | 亚洲一区二区五十路激情中出自拍 | 美国一级毛片在线观看 | 男人天堂高清无码 | 国产美女白丝喷水在线观看 | 国产欧美在线观看不卡高清 | 一级 a一级 a 免费观看免免黄 | 欧美性受XXXX黑人XX | 国产欧美一区二区精品性 | 亚洲一区在线入口 | 综合一区中文字幕 | 中文字幕一区二区三区伦理影院 | 久久人人爽A片国产传媒 | 亚洲一区二区影院 | 81人妻精品无码视频 | 精品黑人一区二区三区国语馆 | 国产精品在线久久三级片 | 7777色情网黄A片免费看蜜臀 |