吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
av无码在线,男人的好免费观看直播,精品无码国产自产拍在线观看蜜
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-phospho-AQP2(Ser264+261)/PE-Cy5.5 Conjugated antibody (bs-4610R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-4610R-PE-Cy5.5
英文名稱1 Rabbit Anti-phospho-AQP2(Ser264+261)/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的磷酸化水通道蛋白2抗體
別    名 Aquaporin 2 (phospho S261); p-Aquaporin 2 (phospho S261) ADH water channel; AQP 2; AQP CD; AQP2; AQPCD; Aquaporin 2 collecting duct; Aquaporin CD; Aquaporin2; Aquaporine 2; Collecting duct water channel protein; MGC34501; Water channel protein for renal collecting duct; WCH CD; WCHCD.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
產(chǎn)品類型 磷酸化抗體 
研究領域 腫瘤  細胞生物  信號轉(zhuǎn)導  通道蛋白  細胞粘附分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Dog,  (predicted: Human, Mouse, Rat, Chicken, Pig, Cow, Sheep, )
產(chǎn)品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 30kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthesised phosphopeptide derived from human AQP2 around the phosphorylation site of Ser264/261
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(chǎn)品介紹 background:
This gene encodes a water channel protein located in the kidney collecting tubule. It belongs to the MIP/aquaporin family, some members of which are clustered together on chromosome 12q13. Mutations in this gene have been linked to autosomal dominant, and recessive forms of nephrogenic diabetes insipidus. Belongs to the MIP/aquaporin (TC 1.A.8) family.

Function:
Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient.

Subcellular Location:
Apical cell membrane; Multi-pass membrane protein. Cytoplasmic vesicle membrane; Multi-pass membrane protein. Note=Shuttles from vesicles to the apical membrane.

Tissue Specificity:
Expressed in renal collecting tubules.

Post-translational modifications:
Ser-256 phosphorylation is necessary and sufficient for expression at the apical membrane. Endocytosis is not phosphorylation-dependent.

DISEASE:
Defects in AQP2 are the cause of diabetes insipidus nephrogenic autosomal (ANDI) [MIM:125800]; also known as diabetes insipidus nephrogenic type 2. ANDI is caused by the inability of the renal collecting ducts to absorb water in response to arginine vasopressin. It is characterized by excessive water drinking (polydypsia), excessive urine excretion (polyuria), persistent hypotonic urine, and hypokalemia. Inheritance can be autosomal dominant or recessive.

Similarity:
Belongs to the MIP/aquaporin (TC 1.A.8) family.

Database links:

Entrez Gene: 359 Human

Entrez Gene: 11827 Mouse

Entrez Gene: 25386 Rat

Omim: 107777 Human

SwissProt: P41181 Human

SwissProt: P56402 Mouse

SwissProt: P34080 Rat

Unigene: 130730 Human

Unigene: 20206 Mouse

Unigene: 90076 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
亚洲精品~无码抽插| 亚洲国产精久久久久久久| 人妻少妇精品久久久久久| 女人下边被添全过视频| SAO货撅起你的贱屁股来| 亚洲熟妇AV日韩熟妇在线| 国产精品一区二区久久| 最新中文字幕AV专区| 极品少妇xxxx精品少妇偷拍| 日韩精品久久久久久免费| 国产人妻久久精品二区三区特黄 | 精品久久久久久国产| 色噜噜AV亚洲色一区二区| 国产精品女同一区二区| H漫在线观看| 亚洲国产成人片在线观看无码 | 色婷婷av一区二区三区| 中文字日产幕码三区的做法大全 | 亚洲欧美一区二区三区在线 | 护士的小嫩嫩好紧好爽| 无码人妻久久一区二区三区不卡| 亚洲AV无码乱码在线观看| 羞羞漫画在线观看| 国产精品免费无遮挡无码永久视频| BL漫画网站| 黑人上司粗大拔不出来电影| 国产日韩精品中文字无码| 国内老熟妇对白HDXXXX| 美女露100%双奶头无遮挡| 国产老妇伦国产熟女老妇视频| 国自产拍偷拍精品啪啪| 久久人妻内射无码一区三区| 国产初高中精品无码专区| 乌克兰肥妇黑毛BBW| 亚洲精品国产熟女久久久| 精品亚洲一区二区三区四区五区| A片做爰片仑理片免费看午夜蝴蝶| A级毛片在线观看| 性VODAFONEWIFI另类| 亚洲国产精品无码成人片久久| 国产精品久久久久无码AV色戒 |