97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

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
爆乳大森しずか无码,久久久久一区二区三区,啪啪影视
首頁 > 產品中心 > 一抗 > 產品信息
SLC12A3 Rabbit pAb (bs-7694R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-7694R
英文名稱 SLC12A3 Rabbit pAb
中文名稱 鈉氯離子轉運蛋白抗體
別    名 Na Cl symporter; Na-Cl symporter; NaCl electroneutral thiazide sensitive cotransporter; NCCT; S12A3_HUMAN; slc12a3; Solute carrier family 12(sodium/chloride transporters) member 3; Solute carrier family 12 member 3; Thiazide sensitive Na Cl cotransporter; Thiazide sensitive sodium chloride cotransporter; Thiazide-sensitive sodium-chloride cotransporter; TSC.  
Specific References  (1)     |     bs-7694R has been referenced in 1 publications.
[IF=3.657] Matsubara, Ai. et al. Low-salt diet increases mRNA expression of aldosterone-regulated transporters in the intermediate portion of the endolymphatic sac. Pflug Arch Eur J Phy. 2022 Feb;:1-11  IHC ;  Rat.  
研究領域 腫瘤  心血管  細胞生物  通道蛋白  轉運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human (predicted: Mouse,Rat,Rabbit,Cow,Dog)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 113 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SLC12A3/NCCT: 951-1021/1021 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 Na-K-Cl cotransporters (NKCC) are channel proteins that aid in the transcellular movement of chloride across both secretory and absorptive epithelia. NKCC1 is expressed in muscle cells, neurons, and red blood cells. In the basolateral membrane of secretory epithelia, NKCC1 mediates active chloride secretion. The gene encoding human NKCC1 maps to chromosome 5q23.3. In mice, disruption of the NKCC1 gene leads to deafness and impaired balance. NKCC2 is specifically expressed in the kidney where it mediates active reabsorption of sodium chloride in the thick ascending limb of the loop of Henle. NKCC2 is sensitive to the clinically important diuretics furosemide and bumetanide. The gene encoding human NKCC2 maps to chromosome 15q15-q21 and mutations in this gene lead to Bartter’s syndrome, an inherited hypokalaemic alkalosis. NCCT is a thiazide-sensitive Na-Cl cotransporter that is primarily expressed in the distal convoluted tubule of the kidney where it accounts for a significant fraction of net renal sodium reabsorption. The gene for human NCCT map to chromosome 16q13. Mutations in the gene encoding NCCT cause Gitelman’s syndrome, a subset of Bartter’s syndrome.

Function:
Electrically silent transporter system. Mediates sodium and chloride reabsorption.

Subunit:
Interacts with KLHL3.

Subcellular Location:
Membrane.

Tissue Specificity:
Predominant in kidney.

Post-translational modifications:
Ubiquitinated; ubiquitination is essential for regulation of endocytosis (By similarity). May be ubiquitinated by the BCR(KLHL3) complex.

DISEASE:
Defects in SLC12A3 are the cause of Gitelman syndrome (GS). GS is an autosomal recessive disorder characterized by hypokalemic alkalosis in combination with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. Patients are often asymptomatic or present transient periods of muscular weakness and tetany, usually accompanied by abdominal pain, vomiting and fever. The phenotype is highly heterogeneous in terms of age at onset and severity. Cardinal features such as hypocalciuria and hypomagnesemia might also change during the life cycle of a given patient. GS has overlapping features with Bartter syndrome.

Similarity:
Belongs to the SLC12A transporter family.

SWISS:
P55017

Gene ID:
6559

Database links:

Entrez Gene: 6559 Human

Entrez Gene: 20497 Mouse

Entrez Gene: 54300 Rat

Omim: 600968 Human

SwissProt: P55017 Human

SwissProt: P59158 Mouse

SwissProt: P55018 Rat

Unigene: 669115 Human

Unigene: 25804 Mouse

Unigene: 10467 Rat



版權所有 2004-2026 www.kastlife.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: 日韩中文字幕手机在线观看 | 亚洲国产精品lv | 国产成人在线高清 | 国产成人午夜精华液 | 欧美一区二区三区在线看 | 国产精品222| av久久伊人精品中文字幕 | 欧美性猛交xxxx免费看德国 | 欧美成人免费全部观看天天性色 | giga特摄剧在线官网 | 成人免费A级毛片无码片2023 | 东京一本到熟无码免费视频 | 污污汅18禁在线无遮挡免费观看 | 麻豆乐园 | 蜜桃臀av | 国产精品嫩草影院99网站 | 亚洲人成无码网站在线观看 | 中国性感美女一级黄色影片 | 国产无遮挡无码视频免费软件 | 国产精品久久久亚洲一区 | 免费AV一区二区三区3ATV | 一级在线播放 | 欧美亚洲第一页 | 国产精品福利久久久 | 久久夜色精品亚洲 | 日韩精品123区 | 激情综合婷婷色五月蜜桃 | 午夜视频在线免费播放 | 欧美精品一本久久男人的天堂 | 91剧场在线观看 | 波多野结衣伦理在线观看 | 色婷婷五月天 | av国产精品 | 琪琪午夜成人理论福利片美容院 | 夜色资源网站ye321 | 亚洲成人综合网站 | 成人免费观看视频网站 | 亚洲一区二区三区色噜噜 | 亚洲免费一 | 成人在色线视频在线观看免费大全 | 亚洲婷婷六月的婷婷 |