mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
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  關(guān)于我們  聯(lián)系我們
最近中文字幕视频2019,久久综合久色综合欧美,亚洲欧美综合中文字幕
首頁(yè) > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
STRA6 Rabbit pAb (bs-12351R)  
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@www.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@www.p2b3.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)

產(chǎn)品編號(hào) bs-12351R
英文名稱 STRA6 Rabbit pAb
中文名稱 維甲酸誘導(dǎo)蛋白6抗體
別    名 Stimulated by retinoic acid gene 6 protein homolog; STRA6_HUMAN.  
Specific References  (3)     |     bs-12351R has been referenced in 3 publications.
[IF=6.448] Nishimoto K et al. Dynamics of vitamin A uptake, storage, and utilization in vocal fold mucosa. Mol Metab .2020 Oct;40:101025.  IHC ;  Human/Rat.  
[IF=6.126] Da?a Zupan?i? et al. Vitamin A Rich Diet Diminishes Early Urothelial Carcinogenesis by Altering Retinoic Acid Signaling. Cancers (Basel). 2020 Jun 28;12(7):1712.  IHC-P&IHF-P ;  Mouse.  
[IF=6.126] Da?a Zupan?i?et al. Vitamin A Rich Diet Diminishes Early Urothelial Carcinogenesis by Altering Retinoic Acid Signaling. Cancers (Basel) . 2020 Jun 28;12(7):1712.  IF ;  mouse.  
研究領(lǐng)域 腫瘤  細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  新陳代謝  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human (predicted: Mouse,Rat,Rabbit,Dog,Horse)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 74 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from Human STRA6: 151-250/667 <Extracellular>
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(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 STRA6 is a 667 amino acid, multi-pass cell membrane protein. Stra6 functions as a cell-surface receptor for the complex retinol-retinol binding protein (RBP/RBP4). Ultimately increasing cellular retinol uptake from the retinol-RBP complex, Stra6 removes retinol from RBP/RPB4 and transports it across the plasma membrane, where it is metabolized. Stra6 is broadly expressed, with 4 named isoforms that exist as a result of alternative splicing events. Mutations in the gene encoding Stra6 cause Matthew-Wood Syndrome, also known as Spear Syndrome. This syndrome is characterized by anophtalmia, mild facial dysmorphism and malformations of the heart, lung and diaphragm. The Stra6 gene maps to chromosome 15q24.1.

Function:
Stra6 functions as a high-affinity cell-surface receptor for the complex retinol-retinol binding protein (RBP/RBP4). Stra6 is expressed in the extraembryonic endoderm and expression is also known to be induced by Wnt1. Defects in STRA6 are known to cause of syndromic microphthalmia type 9 (MCOPS9) also known as clinical anophthalmia with mild facial dysmorphism and variable malformations of the lung, heart, and diaphragm or anophthalmia/microphthalmia and pulmonary hypoplasia or Spear syndrome or Matthew-Wood syndrome or pulmonary agenesis, microphthalmia, and diaphragmatic defect.

Subcellular Location:
Cell membrane; multi-pass membrane protein.

Tissue Specificity:
Broad expression. In adult eye expressed in sclera, retina, retinal pigment epithelium, and trabecular meshwork but not in choroid and iris.

DISEASE:
Defects in STRA6 are the cause of microphthalmia syndromic type 9 (MCOPS9) [MIM:601186]; also called Matthew-Wood syndrome or Spear syndrome. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS9 is a rare clinical entity including as main characteristics anophthalmia or severe microphthalmia, and pulmonary hypoplasia or aplasia.
Note=Mutations in STRA6 may be a cause of isolated colobomatous microphthalmia, a disorder of the eye characterized by an abnormally small ocular globe.

SWISS:
Q9BX79

Gene ID:
64220

Database links:

Entrez Gene: 64220 Human

Omim: 610745 Human

SwissProt: Q9BX79 Human

Unigene: 24553 Human



產(chǎn)品圖片
Paraformaldehyde-fixed, paraffin embedded (human placenta); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min;
版權(quán)所有 2004-2026 www.www.p2b3.cn 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
老头鸡巴操老太骚逼| 啊啊啊好疼视频进来| 欧美国产人妖另类色视频| 久久久久久久 亚洲精品| 老头鸡巴操老太骚逼| 99热这里只有精品亚洲| 青娱乐欧美性爱视频| 亚洲国产综合精品 在线 一区| 亚洲一级片在线播放| 久久国产精品二卡| 国产精品自在拍首页| 在线精品亚洲观看不卡欧| 欧美精品一区二区三区四区五区| 欧美高清一二三区| 国产精品白浆一区二区三区| 国产剧情使劲操我逼| 韩国女主播一区二区视频| A级毛片毛片免费观看久| 国产美女裸体视频全免费| 中文字幕一区二区日韩精品蜜臂| 免费国产香蕉视频在线观看| 国产免费无码一区二区视频无码| 美国女人抠插bbb| 无码中文字幕免费一区二区三区| 大鸡巴抽插小穴色虐视频| 91久久高清国语自产拍| 久久久久有精品国产麻豆| 亚洲大尺度无码无码专线一区| 久久久18禁一区二区网| 亚洲一区二区三成人精品| 联系附近成熟妇女| 日韩人妻无码中字一区二区| 欧美精品视频在线| 精品人妻一区二区三区日产乱码| 色逼色逼色逼色逼色逼色| 一区二中文字幕在线看国产一区| 大鸡巴日小美女明星的BB| 亚洲AV无码一区二区三区系列| 精品一区二区av天堂色偷偷| 中文字幕乱码一区二区三区麻豆| 男女真人牲交高潮全过程|