麻豆av资源_日本三级一区_www.狠狠艹_国产精妇在线观看第一区_成人性生交大片免费看中国A片_日本一本久久

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
夜色亚洲,色眯眯av,扒开粉嫩小泬舌头伸进去视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CLCN2/BF647 Conjugated antibody (bs-6470R-BF647)
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-6470R-BF647
英文名稱 Rabbit Anti-CLCN2/BF647 Conjugated antibody
中文名稱 BF647標記的氯離子通道蛋白2抗體
別    名 Chloride Channel 2; Chloride channel protein 2; Chloride channel, voltage sensitive 2; CIC 2; CIC2; ClC-2; CLC2; Clcn2; CLCN2_HUMAN; ECA2; ECA3; EG13; EGI11; EGMA; EJM6; EJM8.  
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  神經生物學  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, Chicken, Dog, Pig, Cow, Horse, Rabbit, .)
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 99kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CLCN2/CLC-2
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:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterized by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent’s disease, a renal disorder characterized by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.

Function:
Voltage-gated chloride channel. Chloride channels have several functions including the regulation of cell volume; membrane potential stabilization, signal transduction and transepithelial transport.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Ubiquitously expressed. Moderately expressed in aortic and coronary vascular smooth muscle cells and expressed at a low level in aortic endothelial cells.

DISEASE:
Defects in CLCN2 are associated with susceptibility to epilepsy, idiopathic generalized type 11 (EIG11) [MIM:607628]. A disorder characterized by recurring generalized seizures in the absence of detectable brain lesions and/or metabolic abnormalities. Generalized seizures arise diffusely and simultaneously from both hemispheres of the brain.
Defects in CLCN2 are associated with juvenile absence epilepsy type 2 (JAE2) [MIM:607628]. JAE is a subtype of idiopathic generalized epilepsy (IGE) characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening and myoclonic seizures.
Defects in CLCN2 are associated with juvenile myoclonic epilepsy type 8 (EJM8) [MIM:607628]. A subtype of idiopathic generalized epilepsy. Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.

Similarity:
Belongs to the chloride channel (TC 2.A.49) family. ClC-2/CLCN2 subfamily.
Contains 2 CBS domains.

Database links:

Entrez Gene: 1181 Human

Entrez Gene: 12724 Mouse

Entrez Gene: 29232 Rat

Omim: 600570 Human

SwissProt: P51788 Human

SwissProt: Q6IPA9 Human

SwissProt: Q9R0A1 Mouse

SwissProt: P35525 Rat

Unigene: 436847 Human

Unigene: 177761 Mouse

Unigene: 11073 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.jywcc.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: 人人妻人人爽人人澡欧美一区 | 巨茎中出肉欲人妻在线视频 | 黑人一区二区三区四区五区 | 色亚洲成人 | 国产毛片18片毛一级特黄 | 九九热综合 | 国产三级农村妇女在线播放 | 成人黄色片在线观看 | 午夜写真福利视频在线观看 | 国产精品亚洲精品一区二区三区 | 51久久成人国产精品麻豆 | 99国产亚洲| 久久久久久久婷婷 | 日本一区二区三区免费在线观看 | 日日摸夜夜添狠狠添欧美 | 久草网视频在线观看 | 免费超级淫片日本高清视频 | 137肉体写真日本裸交 | 少妇欲求不满和邻居在线播放 | 午夜香港三级A三级三点 | 欧美日韩国产精品久久久久 | 老师夹震蛋上课出白浆 | 九一在线| 久热这里只精品国产8 | 中国产一级a毛片四川女 | 日本十八禁视频无遮挡尤物 | 国产综合视频在线 | 99久久伊人精品综合观看 | 成人免费网站在线 | 欧美性生交XXXXX久久久缅北 | 精品视频在线看 | a毛片视频免费观看 | 无码中文字幕色专区 | 久久久经典视频 | 成人天堂视频第一网站 | 中文字幕在线不卡精品视频99 | 91.久久| 色婷婷成人做爰视频免费 | 国产99视频精品免视看7 | 色婷婷综合久久久久中文字幕小说 | 激情综合婷婷色五月蜜桃 |