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  人才招聘  關于我們  聯系我們
人妻少妇被猛烈进入中文字幕,在线视频精品一区,国产精品高清在线观看93
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Slc22a5/PE-Cy7 Conjugated antibody (bs-8149R-PE-Cy7)
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-8149R-PE-Cy7
英文名稱1 Rabbit Anti-Slc22a5/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標記的溶質載體家族蛋白22成員5抗體
別    名 High-affinity sodium-dependent carnitine cotransporter; OCTN2; Organic cation/carnitine transporter 2; S22A5_HUMAN; Slc22a5; Solute carrier family 22 member 5.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  免疫學  信號轉導  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Dog, Pig, Cow, Horse, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 58kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Slc22a5
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:
Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. [provided by RefSeq, Jul 2008].

Function:
Sodium-ion dependent, high affinity carnitine transporter. Involved in the active cellular uptake of carnitine. Transports one sodium ion with one molecule of carnitine. Also transports organic cations such as tetraethylammonium (TEA) without the involvement of sodium. Also relative uptake activity ratio of carnitine to TEA is 11.3.

Subunit:
Interacts with PDZK1.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Strongly expressed in kidney, skeletal muscle, heart and placenta. Highly expressed in intestinal cell types affected by Crohn disease, including epithelial cells. Expressed in CD68 macrophage and CD43 T-cells but not in CD20 B-cells.

DISEASE:
Defects in SLC22A5 are the cause of systemic primary carnitine deficiency (CDSP) [MIM:212140]. CDSP is an autosomal recessive disorder of fatty acid oxidation caused by defective carnitine transport. Present early in life with hypoketotic hypoglycemia and acute metabolic decompensation, or later in life with skeletal myopathy or cardiomyopathy.

Similarity:
Belongs to the major facilitator (TC 2.A.1)

Database links:

Entrez Gene: 6584 Human

Entrez Gene: 29726 Rat

Omim: 603377 Human

SwissProt: O76082 Human

SwissProt: O70594 Rat

Unigene: 443572 Human

Unigene: 8844 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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: 无遮挡无码视频在线观看免费播放漫画| 久久不见久久见免费视频粉色视频| 精品国产女同脚脚毛片| 国产日韩精品一区二区三区在线观看婷欧美日韩 | 国产在线观看网页版入口线路一| av一本久道久久波多野结衣粉| 亚洲精品一卡2卡3卡三卡四卡免费| 麻豆短视频在线观看成人| 非洲AV无码内射| 午夜精品久久久久久99热蜜桃,香蕉| 精品无码综合一区网 | 国产最新av海角| 亚洲一区二区三区香蕉一本道| 日本动漫资源免费观看| 岛国不卡视频一区在线播放| 亚洲国产成人片在线观看喷水| 韩国美女vip福利一区二区在线| 一级做a爰性色毛片永| 久久人人爽人人人人片男男| 18果冻传媒视频入口秘?| 人妻无码Av大芭蕉伊人| 99精品久久精品一区二区黑牛影视| 色噜噜狠狠色综合日日麻| 成人午夜看片在线观看,欧美| 色婷婷国产传媒综合久久| 东北老妇露脸BBBBBBBXXXXXXXHD| 无码人妻精一区二区三区四季 | 亚洲综合久久综合激情久久综合 | 亚洲乱码av中文一区二区蜜臀男同| 久久久久久久久久96久久| 97国产超薄黑色肉色丝袜无码| 日本精品三区 av| 制服丝袜快播变态另类99热在线播放第三页| 免费AV网站在线观看| 一区二区三区无码在观看线国产| 精品无码一级毛片免费| 亚洲不卡av影片在线播放视频| 暴力av中文在线观看网站| 久久夜色精品国产噜噜亚洲AV岳母 | 一级毛片私人影院免费 亚洲红桃 一级毛片一级毛片一级毛片AAAB 一级毛片一级毛片一级毛片二十五 | 亚洲国产一区在线张津|