参阅全部 Fibronectin 一抗
描述小鼠单克隆抗体[IST-9] to Fibronectin
特异性This antibody reacts with an epitope (PEDGIHELFP) located in the ED-A sequence of cellular fibronectin (it therefore only detects the cFN and not extracellular FN (plasma FN)). (Liao et al.) The ED-A segment can be included or omitted from the molecule depending on the pattern of splicing of the mRNA precursors. In transformed or tumour derived cells the ED-A segment is about 10-times higher than in FN from normal fibroblasts, and it may therefore be a significant marker for malignancy (Borsi et al., and others).
经测试应用适用于: WB, RIA, ELISA, IHC-Fr, ICC/IF, Other, Blocking, IHC-Pmore details
种属反应性与反应: Rat, Chicken, Cow, Dog, Human, Pig, Monkey
预测可用于: Mouse, Rabbit
表位Liao et al: Clone IST-9, binds to the Ile43 and His44 residues within ED-A in a conformationally dependent fashion, implicating the loop region encompassing both residues as critical for mediating ED-A function. The conformational domain C-C'-E of rat EIIIA encompassing the His44 residue is crucial for constituting the IST-9 epitope.
- Positive controls listed in abreviews: WB: Human dermal fibroblast whole cell lysate, treated with TGF beta 1. Human platelets ( treated with ADP for 30 minutes). IHC-P: Canine myocardial infarct. tissue. Rat kidney tissue. Human small intestine tissue. ICC/IF: Human esophageal epithelial cells.
存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Concentration information loading...
纯度Immunogen affinity purified
Our Abpromise guarantee covers the use of ab6328 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||Use a concentration of 1 - 5 µg/ml.|
|RIA||Use at an assay dependent concentration.|
|AP||Use at an assay dependent concentration.|
|IHC-Fr||Use at an assay dependent concentration.
Concentration of IST-9 in IHC-fr - depending on the system - is 0.1 to 2 micrograms per ml.
IST-9 works very well using all iHC-fr procedures.
|Other||Use at an assay dependent concentration.|
|Blocking||Use at an assay dependent concentration. PubMed: 20643910|
|IHC-P||1/100 - 1/200. Perform enzymatic antigen retrieval before commencing with IHC staining protocol.
Concentration of IST-9 in IHC-P is - depending on the system - 2-10 micrograms per ml.
功能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. Involved in osteoblast compaction through the fibronectin fibrillogenesis cell-mediated matrix assembly process, essential for osteoblast mineralization. Participates in the regulation of type I collagen deposition by osteoblasts.
Anastellin binds fibronectin and induces fibril formation. This fibronectin polymer, named superfibronectin, exhibits enhanced adhesive properties. Both anastellin and superfibronectin inhibit tumor growth, angiogenesis and metastasis. Anastellin activates p38 MAPK and inhibits lysophospholipid signaling.
组织特异性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.
疾病相关Glomerulopathy with fibronectin deposits 2
序列相似性Contains 12 fibronectin type-I domains.
Contains 2 fibronectin type-II domains.
Contains 16 fibronectin type-III domains.
发展阶段Ugl-Y1, Ugl-Y2 and Ugl-Y3 are present in the urine from 0 to 17 years of age.
It is not known whether both or only one of Thr-2064 and Thr-2065 are/is glycosylated.
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).
Phosphorylated by FAM20C in the extracellular medium.
Proteolytic processing produces the C-terminal NC1 peptide, anastellin.
细胞定位Secreted, extracellular space, extracellular matrix.
- Information by UniProt
- CIG antibody
- Cold insoluble globulin antibody
- Cold-insoluble globulin antibody
All lanes : Anti-Fibronectin antibody [IST-9] (ab6328) at 1/2000 dilution
Lane 1 : Human dermal fibroblast whole cell lysate, untreated
Lane 2 : Human dermal fibroblast whole cell lysate, treated with TGF beta 1
Lysates/proteins at 10 µg per lane.
All lanes : HRP-conjugated Goat anti-mouse monoclonal at 1/3000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Exposure time: 15 seconds
Blocked with 5% milk for 1 hour at 20°C.
Extracellular matrix expression pattern.
Fibronectin was displayed in microtissues after ten days. (Bar in A549/SV80 monocultures: 50 μm, bar in all other microtissues: 100 μm); Secretion of fibronectin could be observed in microtissues containing fibroblasts, whereas in all tumour cell monocultures no fibronectin secretion could be detected.
Correlation of blood vessel diameter and blood vessel coverage with ECM components.
(PANEL C shown)
(A–D) Blood vessels were visualized by endomucin (green) and coverage of the blood vessel was measured using laminin (red) (A), collagen I (B), fibronectin (C), and collagen I (D). Scale bar: 50 µm.
Anti-Fibronectin antibody [IST-9] (ab6328) at 1/1000 dilution + whole cell lysate prepared from human platelets ( treated with ADP for 30 minutes) at 20 µg
HRP conjugated donkey anti-mouse polyclonal at 1/10000 dilution
Developed using the ECL technique.
Exposure time: 2 minutes
Blocked with 5% milk for 1 hour at 22°C.
ab6328 positively staining paraffin fixed canine myocardial infarct. tissue (1/200). The images demonstrate the time course of fibronectin deposition in reperfused canine myocaridal infarcts.
a: 24 hrs
b: 7 days
c: 28 days of reperfusion.
Secondary: Biotin conjugated goat anti mouse. Detection was achieved using DAB.
This image is an edited version of an image submitted courtesy of an Abreview by Marcin Dobaczewski. We do not have any further information relating to this image.
Formalin fixed paraffin embedded rat kidney stained with ab6328 at a dilution of 1:100 after proteinase K digestion.
The image was kindly supplied as part of the review submitted by Elizabeth Chlipala.
ab6328 staining Fibronectin in human small intestine tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections).
Tissue was fixed with paraformaldehyde and antigen retrieval was by heat mediation in a Tris-EDTA buffer pH 9.0. Samples were incubated with primary antibody (1/50 in blocking buffer) for 30 minutes at 20°C. An undiluted HRP-conjugated Goat anti-mouse polyclonal was used as the secondary antibody.
ab6328 staining fibronectin in human esophageal epithelial cells by ICC/IF (Immunocytochemistry/immunofluorescence).
Cells were fixed with PFA, permeabilized with 1% Triton X-100 in PBS and blocked with 0.25% serum free protein blocker for 20 minutes at 28°C. Samples were incubated with primary antibody (1/100) for 2 hours at 28°C. ab6785 (1/800) was used as the secondary antibody.
This photo shows Fibronectin localization in the extracellular matrix of monolayer culture of human esophageal epithelial cells (Het-1A). Nuclei were counterstained with propidium iodide.
This product has been referenced in:
- Molina-Molina M et al. Anti-fibrotic effects of pirfenidone and rapamycin in primary IPF fibroblasts and human alveolar epithelial cells. BMC Pulm Med 18:63 (2018). Read more (PubMed: 29703175) »
- Lin T et al. Hydrogel derived from porcine decellularized nerve tissue as a promising biomaterial for repairing peripheral nerve defects. Acta Biomater 73:326-338 (2018). WB . Read more (PubMed: 29649641) »