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  關于我們  聯系我們
中文午夜乱理片无码,国产乱子伦精品免费无码专区 ,久久人人爽人人爽人人片av高清
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-KCNA5/APC Conjugated antibody (bs-1837R-APC)
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-1837R-APC
英文名稱 Rabbit Anti-KCNA5/APC Conjugated antibody
中文名稱 APC標記的鉀電壓閥門通道混合器相關亞家族成員5抗體
別    名 Potassium voltage-gated channel subfamily A member 5; MGC117058; MGC117059; HCK1; HK2; HPCN1; Kv1; KV1.5; MGC25248; PCN1; Potassium channel 1; Potassium channel insulinoma and islet cell; ATFB7; PCN1; KCNA5_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 神經生物學  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Rabbit, )
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 67kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KCNA5
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 represent the most complex class of voltage-gated ino channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, the function of which could restore the resting membrane potential of beta cells after depolarization and thereby contribute to the regulation of insulin secretion. This gene is intronless, and the gene is clustered with genes KCNA1 and KCNA6 on chromosome 12.

Function:
Mediates the voltage-dependent potassium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a potassium-selective channel through which potassium ions may pass in accordance with their electrochemical gradient. This channel displays rapid activation and slow inactivation. May play a role in regulating the secretion of insulin in normal pancreatic islets. Isoform 2 exhibits a voltage-dependent recovery from inactivation and an excessive cumulative inactivation.

Subunit:
Heterotetramer of potassium channel proteins. Interacts with DLG1, which enhances channel currents. Forms a ternary complex with DLG1 and CAV3 (By similarity). Interacts with UBE2I.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Pancreatic islets and insulinoma.

Post-translational modifications:
Sumoylated on Lys-221, and Lys-536, preferentially with SUMO3. Sumoylation regulates the voltage sensitivity of the channel.

DISEASE:
Familial atrial fibrillation 7 (ATFB7) [MIM:612240]: A familial form of atrial fibrillation, a common sustained cardiac rhythm disturbance. Atrial fibrillation is characterized by disorganized atrial electrical activity and ineffective atrial contraction promoting blood stasis in the atria and reduces ventricular filling. It can result in palpitations, syncope, thromboembolic stroke, and congestive heart failure. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the potassium channel family. A (Shaker) (TC 1.A.1.2) subfamily. Kv1.5/KCNA5 sub-subfamily.

Database links:

Entrez Gene: 3741 Human

Entrez Gene: 16493 Mouse

Entrez Gene: 25470 Rat

Omim: 176267 Human

SwissProt: P22460 Human

SwissProt: Q61762 Mouse

SwissProt: P19024 Rat

Unigene: 150208 Human

Unigene: 222831 Mouse

Unigene: 162789 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: 樱桃视频app在线网站| 久久精品国产96精品亚洲AV| 97久久久久亚洲vA无码区首页 | 一区二区三区视频观看传媒| 亚洲va久久久噜噜噜久久hh | 岛国高清中文字幕aV一区二区三区四区 | 久久人人97超碰精品888| 无遮挡国产高潮视频免费观看,天天曰天天操 | 国产一区三区三区成视频| 久久久久久人妻无码母乳| 婷婷五月深深久久精品|网站| 一区二区三区四区精品视频聊天| 阿v网站在线观看蜜臀av| 国产免费一区二区三区在线观看_| 亚洲色成人网一二三区在线看片| 99久久国产综合精品麻豆,国产A级.... | 99久久综合精品国产首员无码男同| 国产日本Av电影合集 | 亚洲制服丝袜人妻系列AV不卡| 久久久久国产免费网址| 欧美精品一在线发布| 免费一级做a爰片久久毛片潮斗破苍穹人 | 人人超碰人人爱超碰国产AV-av在线 | 午夜宅男在线永久免费观看网站视频| 国产高清一区二区三区四区变态 | 亚洲精品成人片在线播放43| 亚洲国产区男人本色在线观| 精品一区二区三区在线成人3d动漫 | 久久AV秘?一区二区三区水牛 | 东京热本道五月天| 亚洲草在线观看一线二线| 国产午夜精品理论片九九九九久久久九九久久久久久 | 中文字幕中出在线av| 狠狠躁日日躁夜夜躁2022麻豆_1上映时间 | 久久天天躁夜夜躁狠202 | 国产女m调教打屁股 | 国产大片在线播放高清av| 成人插视频小说网址夜| 18禁美女裸体无遮挡免费网站下载 | a级毛片无码视频AAAA流出91| 99精品久久99久久久久胖女人免费视频|