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  人才招聘  關于我們  聯系我們
亚洲不卡av不卡一区二区,97超级碰碰碰碰久久久久,精品乱码久久久久久中文字幕
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Claudin 16/PE-Cy7 Conjugated antibody (bs-13752R-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-13752R-PE-Cy7
英文名稱1 Rabbit Anti-Claudin 16/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標記的緊密連接蛋白16抗體
別    名 Claudin 16; Claudin-16; CLD16_HUMAN; CLDN 16; Cldn16; Paracellin 1; Paracellin-1; PCLN-1; PCLN 1; PCLN1.  
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  信號轉導  細胞粘附分子  內皮細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Cow, Rabbit, Sheep, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 34kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Claudin 16
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:
Tight junctions mediate the regulation of the paracellular pathway between epithelial and endothelial cells. They form close connections to eliminate the extracellular space and regulate the flow of solutes between cells. The human gene PCLN-1 (paracellin-1) is related to the claudin family of integral membrane proteins, which localize to tight junctions. PCLN-1 contains four transmembrane domains and intracellular amino and carboxy termini, characteristic of the other claudin family members, and is detected only at the tight junctions of kidney tissue. PCLN-1 forms an intercellular pore and controls the resorption of magnesium and calcium in the thick ascending limb of Henle (TAL). Mutations in PCLN-1 cause renal magnesium wasting, which may contribute to a rare autosomal recessive disease, renal hypomagnesemia with hypercalciuria and nephrocalcinosis.

Function:
Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Involved in paracellular magnesium reabsorption. Required for a selective paracellular conductance. May form, alone or in partnership with other constituents, an intercellular pore permitting paracellular passage of magnesium and calcium ions down their electrochemical gradients. Alternatively, it could be a sensor of magnesium concentration that could alter paracellular permeability mediated by other factors.

Subcellular Location:
Cell junction; tight junction. Cell membrane.

Tissue Specificity:
Kidney-specific, including the thick ascending limb of Henle (TAL).

DISEASE:
Defects in CLDN16 are the cause of hypomagnesemia type 3 (HOMG3) [MIM:248250]; also known as familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC). HOMG3 is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis. Recurrent urinary tract infections and kidney stones are often observed. In spite of hypercalciuria, patients do not show hypocalcemia.

Similarity:
Belongs to the claudin family.

Database links:

Entrez Gene: 10686 Human

Entrez Gene: 114141 Mouse

Entrez Gene: 155268 Rat

Omim: 603959 Human

SwissProt: Q9Y5I7 Human

SwissProt: Q14BW2 Mouse

SwissProt: Q925N4 Mouse

SwissProt: Q91Y55 Rat

Unigene: 251391 Human

Unigene: 275205 Mouse

Unigene: 43852 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: 欧美性猛交久久久久四虎| 久久精品国产亚洲精品国产亚洲一区二区电影片 | 不卡中文字幕在线观看的av软件 | 日日摸夜夜满无码AⅤ| 精品亚洲一区二区三区在线观看影院 | 草莓黄瓜蜜桃视频app下载成人 | 中文字幕免费视频不卡| 午夜精品久久久久久毛片HD2LINODE中国成熟 | 中文综合久久88久久香港女星孙禾颐 | 久久久久久午夜精品五码| 岛国不卡视频成| 亚洲电影在线播放列表| 精品国产人成亚洲区_一区二区三区不卡| 99精品久久精品一区二区黑牛影视 | 成人免费久久久66| 无码精品人妻一区二区三区ap小说| 精品人妻一二三四区在交换视频| 中文字幕不卡亚洲精品免费观看| 日本孕妇孕交videostv| 岛国无码在线播放蜜臀hd | 一本色道久久88综合亚洲精品|欧美| 人妻过夜无删减版在线看| 成人午夜精品国产情侣一区二三四| 一区二区三区观看男同| 久久精品视频9191| 亚洲一区二区三区香蕉Av网站 | 波多野结衣在线资源ctxl| 色欲久久久天天天综合网| 超碰欧美日韩99| 免费一毛片自拍的| 中文无码精品一区二区三区神马影院午夜视频 | 无码中文字幕日韩专区,亚 | acg里番全彩侵犯本子福利吧0| 丝袜美腿一区二区三区三区三区三区| 高潮喷水AV一区二区同人漫画 | 久久国产护士视频| 亚洲精品无码AV中文永久在线| 国产三级久久精品一区| 少妇精品久久久一区二区三区肉大捧一进一出| 东北妇女精品视频在线播放| 人妻久久久久久|