强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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
精品人妻无码一区二区三区蜜桃一,四川少扫搡BBw搡BBBB,日韩AV一区二区三区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-KCNA5/PE-Cy5.5 Conjugated antibody (bs-1837R-PE-Cy5.5)
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-1837R-PE-Cy5.5
英文名稱 Rabbit Anti-KCNA5/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5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(guī)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 m.nmgps.com 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(yī)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
打开双腿扒开自慰喷水网站 | 国产精品人妻久久久久厨房 | 亚洲综合在线免费 | 日韩欧美精品在线观看 | 不卡的在线免费视频 | 日本无码熟人中文字幕 | 看国产熟妇乱子伦 | 亚洲精品一区杨思敏 | 国产欧美综合一区二区三区 | 东北少妇不戴套对白第一次 | 777琪琪午夜理论片在线观看 | 精品一区二区三区视频 | 国产在线观看免费无码 | 欧美一区二区三区啪啪啪啪 | 国产三级一区二区三区 | 欧美老熟妇乱大交XXXXX动漫 | 日本人妻系列中文字幕 | 百国产乱婬AV免费 | 99久久无码一区人妻贼王 | 91精品人妻互换一区二区 | 无码精品人妻一区二区三区影院 | av免费在线观看免费在线观看 | 日产AAAA一级毛片 | 8x国产AV三区久久久 | 白丝紧致爆乳自慰喷水 | 少妇精品偷拍高潮白浆 | 免费一级婬片A片AAA小说软件 | 无码 精品 国产19 | 国产高清无码在线 | 日韩精品无码人妻第一页 | 国产裸体免费无遮挡 | 国产精品久久久久久久久久不10 | 在线视频2018二页 | 国产一区二区丝袜高跟 | 黑人泄欲一区二区三区 | 成人在线免费观看视频 | 国产寡妇亲子伦一区二区三区四区 | 肉丝祙做爰在线播放无码 | 美女被 又爽 又黄视频免费观看 | 欧一美一色一伦一A片 | 一级A片无码人妻久久久玉蒲团 |