我和丰满岳疯狂做爰,久久久久亚洲AV片无码,亚洲色欲一区二区三区在线观看,疯狂做受XXXX高潮欧美日本

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
白嫩少妇激情无码,精品久久香蕉国产线看观看亚洲,国产精品日本一区二区不卡视频
首頁 > 產品中心 > 一抗 > 產品信息
Polycystin 2 Rabbit pAb (bs-24450R)  
訂購熱線:400-901-9800
訂購郵箱:sales@www.ssxsbs.com
訂購QQ:  400-901-9800
技術支持:techsupport@www.ssxsbs.com
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產品編號 bs-24450R
英文名稱 Polycystin 2 Rabbit pAb
中文名稱 多囊腎蛋白2抗體
別    名 polycystic kidney disease 2; TRPP2; APKD2, C030034P18RIK, MGC138466, MGC138468, PC2, PKD2(includes EG:5311), PKD4, POLYCISTIN-2, POLYCYSTIN 2, RGD1559992, TRPP2; Polycystic kidney disease 2 protein homolog; PC2.  
研究領域 腫瘤  發育生物學  信號轉導  生長因子和激素  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human (predicted: Mouse,Rat,Rabbit,Pig,Cow,Zebrafish,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 106 kDa
檢測分子量
細胞定位 細胞漿 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Polycystin 2: 41-140/968 <Cytoplasmic>
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 This gene encodes a member of the polycystin protein family. The encoded protein is a multi-pass membrane protein that functions as a calcium permeable cation channel, and is involved in calcium transport and calcium signaling in renal epithelial cells. This protein interacts with polycystin 1, and they may be partners in a common signaling cascade involved in tubular morphogenesis. Mutations in this gene are associated with autosomal dominant polycystic kidney disease type 2. [provided by RefSeq, Mar 2011].

Function:
Involved in fluid-flow mechanosensation by the primary cilium in renal epithelium. PKD1 and PKD2 may function through a common signaling pathway that is necessary for normal tubulogenesis. Acts as a regulator of cilium length, together with PKD1. The dynamic control of cilium length is essential in the regulation of mechanotransductive signaling. The cilium length response creates a negative feedback loop whereby fluid shear-mediated deflection of the primary cilium, which decreases intracellular cAMP, leads to cilium shortening and thus decreases flow-induced signaling. Functions as a calcium permeable cation channel.

Subunit:
Forms homooligomers. Isoform 1 interacts with PKD1 while isoform 3 does not. PKD1 requires the presence of PKD2 for stable expression. Interacts with CD2AP. Interacts with HAX1. Interacts with NEK8. Part of a complex containing AKAP5, ADCY5, ADCY6 and PDE4C.

Subcellular Location:
Membrane; Multi-pass membrane protein (Potential). Endoplasmic reticulum. Cell projection, cilium.

Tissue Specificity:
Strongly expressed in ovary, fetal and adult kidney, testis, and small intestine. Not detected in peripheral leukocytes.

DISEASE:
Polycystic kidney disease 2 (PKD2) [MIM:613095]: A disorder characterized by progressive formation and enlargement of cysts in both kidneys, typically leading to end-stage renal disease in adult life. Cysts also occurs in the liver and other organs. It represents approximately 15% of the cases of autosomal dominant polycystic kidney disease. PKD2 is clinically milder than PKD1 but it has a deleterious impact on overall life expectancy. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the polycystin family.
Contains 1 EF-hand domain.

SWISS:
Q13563

Gene ID:
5311

Database links:

Entrez Gene: 5311 Human

Entrez Gene: 353503 Rat

Omim: 173910 Human

SwissProt: Q13563 Human

SwissProt: O35245 Mouse

Unigene: 181272 Human

Unigene: 483692 Mouse

Unigene: 6442 Mouse



多囊腎(polycystic kidney disease)為遺傳性疾病,是腎臟一種先天性異常。雙側腎臟皮髓質均可累及,但在程度上可不同。在遺傳方式上表現為常染色體顯性和常染色體隱性遺傳兩種。
囊內上皮細胞異常增殖是ADPKD的顯著特特之一,處于一種成熟不完全或重發育狀態,高度提示為細胞的發育成熟調控出現障礙,使細胞處于一種未成熟狀態,從而顯示強增殖性。表現為細胞轉運密切相關的Na+-K+-ATP ase的亞單位組合,分布及活性表達的改變;細胞信號傳導異常以及離子轉運通道的變化。細胞外基質異常增生是ADPKD第三種顯著特征。目前許多研究已證明:這些異常均有與細胞生長有關的活性因子的參與。但關鍵的異常環節和途徑尚未明了。因基因缺陷而致的細胞生長改變和間質形成異常,是本病的重要發病機制之一。
產品圖片
Sample: Lane 1: Panc-1 (Human) Cell Lysate at 30 ug Lane 2: A549 (Human) Cell Lysate at 30 ug Lane 3: Huvec (Human) Cell Lysate at 30 ug Lane 4: Siha (Human) Cell Lysate at 30 ug Primary: Anti-Polycystin 2 (bs-24450R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 110 kD Observed band size: 110 kD
版權所有 2004-2026 www.www.ssxsbs.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