强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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  關(guān)于我們  聯(lián)系我們
91精品人妻一区二区三区果冻,国产一级一级毛片,亚洲一区二区三区在线
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Lubricin/PE Conjugated antibody (bs-11175R-PE)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-11175R-PE
英文名稱 Rabbit Anti-Lubricin/PE Conjugated antibody
中文名稱 PE標記的巨核細胞刺激因子/蛋白多糖4/淺表層粘膜蛋白多糖抗體
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.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 信號轉(zhuǎn)導  細胞骨架  細胞外基質(zhì)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Dog, Cow, Rabbit, )
產(chǎn)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 152kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Lubricin/SZP
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:
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.

Function:
Plays a role in boundary lubrication within articulating joints. Prevents protein deposition onto cartilage from synovial fluid by controlling adhesion-dependent synovial growth and inhibiting the adhesion of synovial cells to the cartilage surface.
Isoform F plays a role as a growth factor acting on the primitive cells of both hematopoietic and endothelial cell lineages. soluble molecule that acts as a carrier for insoluble surface-active phospholipid (SAPL). Depletion of lubricin function has been associated with camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP), an arthritic-like autosomal recessive disorder.

Subunit:
Homodimer; disulfide-linked.

Subcellular Location:
Secreted.

Tissue Specificity:
Highly expressed in synovial tissue, cartilage and liver and weakly in heart and lung. Isoform B is expressed in kidney, lung, liver, heart and brain. Isoform C and isoform D are widely expressed.

Post-translational modifications:
N-glycosylated.
O-glycosylated; contains glycosaminoglycan chondroitin sulfate and keratan sulfate.
The disulfide bond between Cys-1146 and Cys-1403 is essential for protein cleavage.

DISEASE:
Defects in PRG4 are the cause of camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) [MIM:208250]; also known as Jacobs syndrome. CACP is an autosomal recessive disorder. Individuals with CACP have normal appearing joints at birth but with advancing age develop joint failure associated with noninflammatory synoviocyte hyperplasia and subintimal fibrosis of the synovial capsule.

Similarity:
Contains 2 hemopexin-like domains.
Contains 2 SMB (somatomedin-B) domains.

Database links:

Entrez Gene: 10216 Human

Entrez Gene: 280867 Cow

Entrez Gene: 96875 Mouse

Omim: 604283 Human

SwissProt: Q92954 Human

SwissProt: Q9JM99 Mouse

Unigene: 647723 Human

Unigene: 329131 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

取消WB;姬,
版權(quán)所有 2004-2026 nmgps.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
成人做爰xXX视频看片 | 亚洲精品一区杨思敏 | 可以免费看黄色视频网站 | 少妇高潮灌满白浆毛片免费看 | 国产人妻无码毛片久久黄 | 姝姝窝人体www聚色窝 | AAA级无码肉欲免费看 | 欧美黑人性爱视频网站 | 成人小视频在线观看 | 91色视频免费观看 | 美女裸体免费视频久久久 | 久久精品亚洲精品国产欧美 | 欧美一区二区三区精品 | 嫩草鲁丝久久精品熟女 | 99久久无码一区人妻A片贼王 | 国产婬妇 視频网站1 | 又黄又粗又硬又长又大 | 成人精品一区二区三区中文字幕 | 四虎最新成人永久网站 | 麻豆乱婬一区二区三区乱码软件 | 国产成人无码久久久久毛片朴信惠 | 免费无码又爽又高潮视频蜜柚视频 | 污污污视频在线观看网站在线观看网站 | 白丝jk糖心视频在线 | 日韩人妻无码一区二区 | 欧一美一交一交一乱一区二区三区 | 強行糟蹋人妻HD中文 | 成人A片产无码免费视频奶头红杏 | 91精品国产乱码污污污 | 国产又粗又猛又爽又黄 | 国产精品高潮呻吟无码 | 国产无码电影在线观看 | 91精品久久久久 | 呦小BBw搡BBBB一线天 | 精品人妻无码区二区三区 | 亚洲精品免费在线 | 成年免费视频黄网站在线观看 | 亚洲+小说+欧美+激情+另类 | 特黄无码人妻丰满少妇啪啪 | 四虎最新成人网站免费 | 国产色情性黄 免费观看 |