Rabbit Polyclonal Integrin alpha 3 antibody. Suitable for WB and reacts with Human, Mouse samples. Cited in 7 publications. Immunogen corresponding to Synthetic Peptide within Human ITGA3 aa 500-550.
pH: 7.2
Preservative: 0.05% Sodium azide
Constituents: 99% PBS
WB | |
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Human | Tested |
Mouse | Expected |
Cow | Predicted |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/500 - 1/1000 | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info 1/500 - 1/1000 | Notes - |
Species | Dilution info | Notes |
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Species Cow | Dilution info - | Notes - |
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Integrin alpha-3/beta-1 is a receptor for fibronectin, laminin, collagen, epiligrin, thrombospondin and CSPG4. Integrin alpha-3/beta-1 provides a docking site for FAP (seprase) at invadopodia plasma membranes in a collagen-dependent manner and hence may participate in the adhesion, formation of invadopodia and matrix degradation processes, promoting cell invasion. Alpha-3/beta-1 may mediate with LGALS3 the stimulation by CSPG4 of endothelial cells migration. (Microbial infection) Integrin ITGA3:ITGB1 may act as a receptor for R.delemar CotH7 in alveolar epithelial cells, which may be an early step in pulmonary mucormycosis disease progression.
CD49c, MSK18, ITGA3, Integrin alpha-3, CD49 antigen-like family member C, FRP-2, Galactoprotein B3, VLA-3 subunit alpha, GAPB3
Rabbit Polyclonal Integrin alpha 3 antibody. Suitable for WB and reacts with Human, Mouse samples. Cited in 7 publications. Immunogen corresponding to Synthetic Peptide within Human ITGA3 aa 500-550.
pH: 7.2
Preservative: 0.05% Sodium azide
Constituents: 99% PBS
ab190731 purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. Purity >95% by SDS-PAGE.
Integrin alpha 3 also known as ITGA3 or alpha 3 is a protein that plays an important role in cell adhesion and signaling. It forms complexes with other integrins to mediate interactions between cells and the extracellular matrix. Integrin alpha 3 is a type I transmembrane protein with a molecular weight of approximately 120 kDa. This protein is primarily expressed in epithelial tissues including the skin kidneys and respiratory tract.
Integrin alpha 3 functions as a cell surface receptor that helps regulate cell migration proliferation and differentiation. It is a part of the alpha-3-beta-1 integrin complex which interacts with extracellular proteins like laminin-5 and collagen. This interaction facilitates the transmission of signals from the outside to the inside of the cell affecting various cellular responses and activities.
Integrin alpha 3 plays a significant role in the cell signaling and communication pathways. It is involved in the pathways like focal adhesion and MAPK signaling. In these pathways integrin alpha 3 interacts with other proteins such as paxillin and FAK (focal adhesion kinase) which are critical for the downstream signaling that regulates cell shape and movement.
Integrin alpha 3 is linked to conditions like skin blistering diseases and cancers particularly those affecting the epithelial tissues. Alterations in integrin alpha 3 expression or function can disturb cell adhesion leading to diseases like epidermolysis bullosa. Additionally in cancer integrin alpha 3 often collaborates with proteins like MMP-9 to promote tumor invasion and metastasis.
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All lanes: Western blot - Anti-Integrin alpha 3 antibody (ab190731)
All lanes: HepG2 cell extract
Predicted band size: 119 kDa
Image collected and cropped by CiteAb under a CC-BY license from the publication
Integrin alpha 3 western blot using anti-Integrin alpha 3 antibody ab190731. Publication image and figure legend from Temoche-Diaz, M. M., Shurtleff, M. J., et al., 2019, Elife, PubMed 31436530.
ab190731 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab190731 please see the product overview.
Two biochemically distinct sEV sub-populations are released by MDA-MB-231 cells.(a) Schematic showing the two-step purification methodology. Differential ultracentrifugation was followed by buoyant density flotation in a linear iodixanol gradient (Figure 1—figure supplement 1). (b) Immunoblot across the iodixanol gradient for classical sEV markers as well as other non-vesicular RNP components. The two discrete sub-populations are indicated. CD63, a glycosylated protein, migrates heterogeneously. (c) Quantification of individual proteins as in 1b. The black line delineates the maximum signal across the gradient showing three distinctive areas. The first, second and third peak represent the vLD, vHD and non-vesicular RNP fractions. (d) Nanoparticle tracking analysis showing the size distribution of the vHD and vLD sub-populations. The high-speed pellet is also shown. (d) Quantification of the particle number per sEV sub-population using Nanoparticle tracking analysis. Data plotted are from two independent experiments; error bars represent standard deviation from independent samples. (e) Bioanalyzer analysis of the vHD and vLD RNA. The high-speed pellet RNA is also shown.Linearity of iodixanol density gradient.Calculated iodixanol fraction densities collected from the top to bottom of the gradient (fractions 1 to 25) as measured by refractometry (Figure 1—figure supplement 1—source data 1). Fractions were collected post 160,000 g ultracentrifugation (Figure 1a). In red, fractions corresponding to the vLD sub-population. In blue, fractions corresponding to the vHD sub-population.10.7554/eLife.47544.004Figure 1—figure supplement 1—source data 1.Refraction index and calculated densities of the fractions across the gradient (31 fractions in total).Refraction index and calculated densities of the fractions across the gradient (31 fractions in total).
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