超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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
欧美精品一区二区三区免费视频 ,久操福利,美女粉嫩极品国产在线2020
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@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.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 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.ggggww.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: 中文字幕乱在线伦视频中文字幕乱码在线 | 国产一区二区看久久 | 午夜影院伦理片 | 久久精品视频导航 | 欧美xxxx喷水 | 欧美久久一级片 | 国产美女被遭高潮免费网站 | 在线免费视频日韩 | 亚洲天堂成人网 | 粉嫩av一区二区 | 91杏吧在线观看 | 久久久久久久尹人综合网亚洲 | 大狼拘与少妇牲交 | 女人被狂躁高潮啊的视频在线看 | 国产精品久久久久77777丨 | 欧美午夜无码大片免费看 | 欧美aaaa高清乱码视频 | 日本成a人片在线观看日本 久久婷婷五月综合色国产免费观看 | 国产无遮挡18禁无码网站免费 | 日韩卡一卡二无线乱码新区仙踪林 | 天天干天天射天天操天天摸 | 老司机深夜福利视频 | 在线观看AV片永久免费 | wc凹凸撒尿间谍女厕hd | 久久久亚洲精品无码 | 国产成人精品999在线观看 | 欧美日韩久久久精品A片妖精 | 黄色a三级| 日韩成人极品在线内射3p蜜臀 | 在线免费视频一区二区 | 黄色国产免费看 | 精品久久久久久久久久久久久久久久 | 春色校园亚洲愉拍自拍 | 亚洲国产aa | 大学生寝室白袜自慰gay网站 | 亚洲成av人片在线观看麦芽 | 欧美日国产 | 亚洲精品一区二区三区四区高清 | 伊人亚洲精品 | 成人超碰在线观看 | 99久久人妻无码精品系列蜜桃 |