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
中国产公妇仑在线观看,国产永久在线,mm1313亚洲国产精品一区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ROM-K/Kcnj1/APC Conjugated antibody (bs-2960R-APC)
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-2960R-APC
英文名稱 Rabbit Anti-ROM-K/Kcnj1/APC Conjugated antibody
中文名稱 APC標記的ATP調節鉀離子通道ROM K抗體
別    名 ROM K; ROM-K; inwardly rectifying subfamily J member 1; ATP regulated potassium channel ROM K; ATP sensitive inward rectifier potassium channel 1; ATP-regulated potassium channel ROM-K; ATP-sensitive inward rectifier potassium channel 1; Inward rectifier K(+) channel Kir1.1; inwardly rectifying K+ channel; IRK1_HUMAN; KCNJ 1; KCNJ; Kcnj1; Kir 1.1; Kir1.1; Potassium channel; Potassium channel inwardly rectifying subfamily J member 1; potassium inwardly-rectifying channel J1; ROMK 1; ROMK 2; ROMK; ROMK1; ROMK2.  
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  信號轉導  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
產品應用 Flow-Cyt=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 45kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ROM-K/KCNJ1
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:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

Function:
In the kidney, probably plays a major role in potassium homeostasis. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. This channel is activated by internal ATP and can be blocked by external barium.

Subunit:
Interacts with SGK1 and SLC9A3R2/NHERF2.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
In the kidney and pancreatic islets. Lower levels in skeletal muscle, pancreas, spleen, brain, heart and liver.

Post-translational modifications:
Phosphorylation at Ser-44 by SGK1 is necessary for its expression at the cell membrane.

DISEASE:
Defects in KCNJ1 are the cause of Bartter syndrome type 2 (BS2) [MIM:241200]; also termed hyperprostanglandin E syndrome 2. BS refers to a group of autosomal recessive disorders characterized by impaired salt reabsorption in the thick ascending loop of Henle with pronounced salt wasting, hypokalemic metabolic alkalosis, and varying degrees of hypercalciuria. BS2 is a life-threatening condition beginning in utero, with marked fetal polyuria that leads to polyhydramnios and premature delivery. Another hallmark of BS2 is a marked hypercalciuria and, as a secondary consequence, the development of nephrocalcinosis and osteopenia.

Similarity:
Belongs to the inward rectifier-type potassium channel (TC 1.A.2.1) family. KCNJ1 subfamily.

Database links:

Entrez Gene: 3758 Human

Entrez Gene: 56379 Mouse

Entrez Gene: 24521 Rat

Omim: 600359 Human

SwissProt: P48048 Human

SwissProt: O88335 Mouse

SwissProt: P35560 Rat

Unigene: 527830 Human

Unigene: 390168 Mouse

Unigene: 22609 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: 中国黄色一片 | 美女视频黄免费观看 | 他掀开裙子舌头伸进去在线观看 | 国产精品666tv成人影院 | 国产精品s | 欧美极品色午夜在线视频 | 国产成人亚洲精品无码综合原创 | 欧洲一卡2卡三卡4卡乱码毛1 | 美国经典三级 | 国产精品美女久久久久久久久久久 | 91精品一区二区三区蜜臀 | 美日欧激情AV大片免费观看 | 另类在线视频 | www深夜成人| 99热都是精品久久久久久 | 婷婷色综合久久 | 人妻系列无码中文字幕专区 | 黄色免费观看视频 | 公车上玩弄白嫩少妇 | 久久嫩草 | 亚洲宅男网av | 日韩码有限公司在线观看 | 欧美成人看片黄a免费看 | 想看一级黄色 | 欧美一级播放 | 任你操这里只有精品 | 国产精品亚洲综合一区二区三区 | 人与禽性视频77777交片 | 最近2019年日本中文免费字幕 | 香蕉成人国产精品免费看网站 | 国产一区二区三区久久20p | 香港a毛片免费全部播放 | VIDEOS日本熟妇人妻多毛 | 久久久久人妻精品一区蜜桃 | 一级一毛片a级毛片 | 国产91视频在线 | 4虎永久 | 亚洲春色Aⅴ无码专区在线播放 | 新白娘子传奇免费50集 | 欧美精品九九99久久 | 在线超碰免费 |