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
亚洲成a∨人片在线观看无码,欧美性xxxx禁忌,亚洲色婷婷综合久久
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-SCN1B/PE-Cy7 Conjugated antibody (bs-6687R-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-6687R-PE-Cy7
英文名稱 Rabbit Anti-SCN1B/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標記的鈉離子通道β1抗體
別    名 GEFSP1; SCN1B_HUMAN; sodium channel beta 1 subunit; Sodium channel subunit beta 1; Sodium channel subunit beta-1; Sodium channel voltage gated type I beta.  
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  信號轉導  通道蛋白  細胞膜受體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, )
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 22kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SCN1B
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:
Crucial in the assembly, expression, and functional modulation of the heterotrimeric complex of the sodium channel. The subunit beta-1 can modulate multiple alpha subunit isoforms from brain, skeletal muscle, and heart. Its association with neurofascin may target the sodium channels to the nodes of Ranvier of developing axons and retain these channels at the nodes in mature myelinated axons.
Tissue specificity; Abundantly expressed in skeletal muscle, heart and brain.

Function:
Crucial in the assembly, expression, and functional modulation of the heterotrimeric complex of the sodium channel. The subunit beta-1 can modulate multiple alpha subunit isoforms from brain, skeletal muscle, and heart. Its association with neurofascin may target the sodium channels to the nodes of Ranvier of developing axons and retain these channels at the nodes in mature myelinated axons.

Subunit:
The voltage-sensitive sodium channel consists of an ion conducting pore forming alpha-subunit regulated by one or more beta-1, beta-2 and beta-3. Beta-1 and beta-3 are non-covalently associated with alpha, while beta-2 is covalently linked by disulfide bonds. Beta-1 or beta-3 subunits associate with neurofascin. Associates with SCN10A (By similarity).

Subcellular Location:
Membrane; Single-pass type I membrane protein.

Tissue Specificity:
The overall expression of isoforms 1 and 2 is very similar. Isoform 1 is abundantly expressed in skeletal muscle, heart and brain. Isoform 2 is highly expressed in brain and skeletal muscle and present at a very low level in heart, placenta, lung, liver, kidney and pancreas. In brain, isoform 2 is most abundant in the cerebellum, followed by the cerebral cortex and occipital lobe, while isoform 1 levels are higher in the cortex compared to the cerebellum. Isoform 2 is expressed in many regions of the brain, including cerebellar Purkinje cells, cortex pyramidal neurons and many of the neuronal fibers throughout the brain (at protein level). Also detected in dorsal root ganglion, in fibers of the spinal nerve and in cortical neurons and their processes (at protein level).

DISEASE:
Defects in SCN1B are the cause of generalized epilepsy with febrile seizures plus type 1 (GEFS+1) [MIM:604233]. Generalized epilepsy with febrile seizures-plus refers to a rare autosomal dominant, familial condition with incomplete penetrance and large intrafamilial variability. Patients display febrile seizures persisting sometimes beyond the age of 6 years and/or a variety of afebrile seizure types. GEFS+ is a disease combining febrile seizures, generalized seizures often precipitated by fever at age 6 years or more, and partial seizures, with a variable degree of severity.
Defects in SCN1B are the cause of Brugada syndrome type 5 (BRGDA5) [MIM:612838]. A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs (called ventricular fibrillation), the individual will faint and may die in a few minutes if the heart is not reset.

Similarity:
Belongs to the sodium channel auxiliary subunit SCN1B (TC 8.A.17) family.
Contains 1 Ig-like C2-type (immunoglobulin-like) domain.

Database links:

Entrez Gene: 6324 Human

Entrez Gene: 20266 Mouse

Entrez Gene: 29686 Rat

Omim: 600235 Human

SwissProt: Q07699 Human

SwissProt: P97952 Mouse

SwissProt: Q00954 Rat

Unigene: 436646 Human

Unigene: 1418 Mouse

Unigene: 4958 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: 久久久久久久综合狠狠综合国模无码一区二区| 国产成人久久精品激情日韩电影免费| 草莓视频在线在线播放黄| 一本色道久久综合亚洲精品酒店| 中文字幕乱码人妻一区二区三区,99精品久久久久久 | 亚洲国产一二三精品无码不卡 站长工具| 亚洲伊人久久综合影院五月天美传媒 | 一本无码在线观看免费九九| 亚洲精品资源在线播| 日本人妻中文字幕视频| 黄色蜜桃网站黄色| 77777亚洲午夜久久多人_狠狠色噜噜 | 国产剧情高颜值极品在线视频| 狠狠躁日日躁夜夜躁2022麻豆_1上映时间| 国产自啪精品视频网站丝袜app | 7777久久亚洲中文字幕水蜜桃| 艳妇乳欲伦岳| 日日摸夜夜添夜夜添牛牛| 精品视频一区二区三区免费观看视频在线 | 99人妻人人做人碰人人爽| 亚洲中文字阿阿| 亚洲m码 欧洲s码sss222岁| 国产在线精品二区另类| 亚洲色欲综合网网曝热点| 精品久久久久久无码国产免费网站| 制服丝袜在线亚洲1| 久久精品无码中文字幕_中文无码日| 中文字幕在线视频第一页制服丝袜 | 久久久受WWW免费人成| 中文国产成人精品久久久久久精品国产 | 五月天婷婷在线播放综合| 国产V亚洲V天堂无码卡通| 无码国内精品人妻少妇蜜桃视频|亚洲| 国产亚洲一区二区三区在线MV| 亚洲国产婷婷综合在线精品_亚洲国产综合精品 | 中文精品一卡2卡3卡4卡三卡四卡 中文久久字幕波多希岛观看 | 美女粉嫩AV视频| 一本在线不卡视频一二区| 喝尿变态重口小说| 无遮挡又黄又刺激的视频视频| 粉嫩AV四季AV绯色AV第一区|