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

潤(rùn)滑素抗體,Lubricin抗體

更新時(shí)間:2022-05-26點(diǎn)擊次數(shù):491

產(chǎn)品名稱(chēng):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(lái)源:Rabbit

克隆類(lèi)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(duì)應(yīng)的抗原

Lubricin抗原

Lubricin antigen

 



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