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首页 > 产品中心 > 抗体系列 > 一抗

货号:GZ8043

Fibronectin (10W14) Rabbit Monoclonal Antibody

FN1;FN;Fibronectin;FN;Cold-insoluble globulin;CIG

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别名 FN1;FN;Fibronectin;FN;Cold-insoluble globulin;CIG
基因名称 FN1
蛋白名称 Fibronectin
推荐应用
反应物种 Human,Mouse,Rat
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2335
Human Swissprot No. P02751
Human Swissprot Link http://www.uniprot.org/uniprotkb/P02751/entry
Mouse Gene ID 14268
Mouse Gene Link http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=14268
Mouse Swissprot No. P11276
Mouse Swissprot Link http://www.uniprot.org/uniprot/P11276
Rat Swissprot No. P04937
Rat Swissprot Link http://www.uniprot.org/uniprot/P04937
稀释度 IHC-P 1:1000-1:5000, WB 1:2000-1:10000, IF-P/IF-F/IF-ICC 1:200-1:1000, ELISA 1:5000-1:20000
参考分子量 285kDa
预测分子量 263kDa
运输及保存条件 Biological ice bag transportation. Store at -20°C for at least 12 months(Do not lower than -25°C). Avoid freeze/thaw cycles
宿主 Rabbit
同种型 Monoclonal, rabbit, IgG, Kappa
背景介绍 This gene encodes fibronectin, a glycoprotein present in a soluble dimeric form in plasma, and in a dimeric or multimeric form at the cell surface and in extracellular matrix. The encoded preproprotein is proteolytically processed to generate the mature protein. Fibronectin is involved in cell adhesion and migration processes including embryogenesis, wound healing, blood coagulation, host defense, and metastasis. The gene has three regions subject to alternative splicing, with the potential to produce 20 different transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing. The full-length nature of some variants has not been determined. [provided by RefSeq, Jan 2016],
信号通路 Focal adhesion;ECM-receptor interaction;Regulates Actin and Cytoskeleton;Pathways in cancer;Small cell lung cancer;
功能 alternative products:Additional isoforms seem to exist,developmental stage:Ugl-Y1, Ugl-Y2 and Ugl-Y3 are present in the urine from 0 to 17 years of age.,disease:Defects in FN1 are the cause of glomerulopathy with fibronectin deposits type 2 (GFND2) [MIM:601894]; also known as familial glomerular nephritis with fibronectin deposits or fibronectin glomerulopathy. GFND is a genetically heterogeneous autosomal dominant disorder characterized clinically by proteinuria, microscopic hematuria, and hypertension that leads to end-stage renal failure in the second to fifth decade of life.,function:Fibronectins bind cell surfaces and various compounds including collagen, fibrin, heparin, DNA, and actin. Fibronectins are involved in cell adhesion, cell motility, opsonization, wound healing, and maintenance of cell shape. Interaction with TNR mediates inhibition of cell adhesion and neurite outgrowth.,online information:Fibronectin entry,PTM:Forms covalent cross-links mediated by a transglutaminase, such as F13A or TGM2, between a glutamine and the epsilon-amino group of a lysine residue, forming homopolymers and heteropolymers (e.g. fibrinogen-fibronectin, collagen-fibronectin heteropolymers).,PTM:It is not known whether both or only one of Thr-2064 and Thr-2065 are/is glycosylated.,PTM:Sulfated.,similarity:Contains 12 fibronectin type-I domains.,similarity:Contains 16 fibronectin type-III domains.,similarity:Contains 2 fibronectin type-II domains.,subunit:Mostly heterodimers or multimers of alternatively spliced variants, connected by 2 disulfide bonds near the carboxyl ends; to a lesser extent homodimers. Interacts with FBLN1, AMBP, TNR, LGALS3BP and COL13A1. Interacts with FBLN7.,tissue specificity:Plasma FN (soluble dimeric form) is secreted by hepatocytes. Cellular FN (dimeric or cross-linked multimeric forms), made by fibroblasts, epithelial and other cell types, is deposited as fibrils in the extracellular matrix. Ugl-Y1, Ugl-Y2 and Ugl-Y3 are found in urine.,
纯化 Protein A
Clonality Monoclonal

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