国内自拍视频在线,使劲好爽好舒服在线播放,国产精品日韩在线亚洲一区,福利利视频在线观看免费

免費(fèi)咨詢熱線

15121004110

技術(shù)文章

TECHNICAL ARTICLES

當(dāng)前位置:首頁技術(shù)文章潤滑素抗體,Lubricin抗體

潤滑素抗體,Lubricin抗體

更新時間:2022-05-26點(diǎn)擊次數(shù):492

產(chǎn)品名稱:Anti-Lubricin antibody

Rabbit Anti-Lubricin  

別名:Superficial zone proteoglycan; articular superficial zone protein; bG174L6.2; CACP; camptodactyly arthropathy coxa vara pericarditis syndrome gene; FLJ32635; HAPO; Jacobs camptodactyly-arthropathy-pericarditis syndrome gene; JCAP; megakaryocyte stimulating factor; MSF; PRG 4; PRG4; proteoglycan 4; Proteoglycan4; Superficial zone proteoglycan; SZP; PRG4_HUMAN.  

來源:Rabbit

克隆類型:polyclonal 

濃度:1mg/ml

亞型:IgG

應(yīng)用: WB=1:500-1000   ELISA=1:500-1000 

IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500

 反應(yīng): Human,Mouse Rat  

免疫原:KLH conjugated synthetic peptide derived from human Lubricin

Lubricin, also designated proteoglycan-4 or megakaryocyte stimulating factor, is important for boundary lubrication within articulating joints. It is a disulfide-linked homodimer (between Cysteine 1146 and Cysteine 1403) that is essential for protein cleavage. Lubricin inhibits synovial cell adhesion to the cartilage surface, but also prevents the deposition of proteins from synovial fluid onto cartilage. Lubricin is highly expressed in cartilage, liver and synovial tissue. Defects in the gene encoding for lubricin can cause Jakobs syndrome, also designated camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP). CACP is an autosomal recessive disorder characterized by joint failure associated with noninflammatory synoviocyte hyperplasia and subinitimal fibrosis of the synovial capsule. Lubricin undergoes different levels of glycosylation and may be detected at varying molecular weights. 

保存:-20
保質(zhì)期:1

 上海允麥,供應(yīng)Lubricin抗體對應(yīng)的抗原

Lubricin抗原

Lubricin antigen

 



掃碼加微信

服務(wù)熱線

021-34553900

上海市青浦區(qū)

562398366@qq.com

Copyright © 2025上海允麥生物科技有限公司 All Rights Reserved    備案號:滬ICP備20013035號-2

技術(shù)支持:化工儀器網(wǎng)    管理登錄    sitemap.xml

久久久久精品国产色哟哟| 精品久久久久久久久小说| 在线天堂中文最新版网| 中文字幕一区二区720p| 国产日韩欧美日日骚一区| 中文字幕亚洲无线码| 在线 中文字幕 第一页| 国产美女在线永久免费网站| 视频区图片区小说区在线| 黑人大吊孕妇性交操操操| 久久久久久久曰本免费看| 精品女同一区二区三区不卡| 亚洲av成人片无码| 露脸超嫩97后在线播放| 911天堂国产在线观看| 国产精品久久久久乳精品爆| 青青伊人网在线视频播放| 国产精品123| 三级黄在线播放| 亚洲欧洲精品成人久久曰影片| 日韩精品一区二区在线电影| 欧美日韩在线亚洲二区综二| 亚洲av日韩综合一区尤物| 日韩欧美国产综合在线播放 | 国产一级二级三级在线影院| 在线观着免费观看国产黄| 久久精品国产亚洲av日韩| 国产精品18久久久久久不| 国产国产人精品视频69| 国产成人影视久久久综合| 精品伦精品一区二区三区| 变态女人的骚逼亚洲视频| 凡人修仙传动漫在线观看| 十八禁在线永久免费观看| 日韩国产精品亚洲а∨天堂免 | 久久亚洲av不卡一区二区| 欧美成人三级伦在线观看| 97视频在线观看免费观看| 少妇无码AV无码转区线| 欧美一区二区三区色噜噜| 国产91av在线免费播放|