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Human Monoclonal ITGA2 Primary Antibody for CyTOF, FACS - ABIN4900791
Kamata, Takada: Direct binding of collagen to the I domain of integrin alpha 2 beta 1 (VLA-2, CD49b/CD29) in a divalent cation-independent manner. in The Journal of biological chemistry 1994
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Mouse (Murine) Monoclonal ITGA2 Primary Antibody for BR, FACS - ABIN1176973
Arase, Saito, Phillips, Lanier: Cutting edge: the mouse NK cell-associated antigen recognized by DX5 monoclonal antibody is CD49b (alpha 2 integrin, very late antigen-2). in Journal of immunology (Baltimore, Md. : 1950) 2001
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Mouse (Murine) Monoclonal ITGA2 Primary Antibody for BR, FACS - ABIN2689302
Chen, Paul: A population of CD62Llow Nk1.1- CD4+ T cells that resembles NK1.1+ CD4+ T cells. in European journal of immunology 1998
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Mouse (Murine) Monoclonal ITGA2 Primary Antibody for CyTox, IHC (fro) - ABIN2689301
Moore, von Freeden-Jeffry, Murray, Zlotnik: Inhibition of gamma delta T cell development and early thymocyte maturation in IL-7 -/- mice. in Journal of immunology (Baltimore, Md. : 1950) 1996
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Mouse (Murine) Monoclonal ITGA2 Primary Antibody for IHC (fro), FACS - ABIN2689298
Ortaldo, Winkler-Pickett, Mason, Mason: The Ly-49 family: regulation of cytotoxicity and cytokine production in murine CD3+ cells. in Journal of immunology (Baltimore, Md. : 1950) 1998
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Mouse (Murine) Monoclonal ITGA2 Primary Antibody for BR, IHC (fro) - ABIN2689303
Hemler: VLA proteins in the integrin family: structures, functions, and their role on leukocytes. in Annual review of immunology 1990
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Human Monoclonal ITGA2 Primary Antibody for FACS, IP - ABIN2480690
Katayama: [Basic and experimental studies of the renin-angiotensin-aldosterone system in diabetes mellitus]. in Nihon Naibunpi Gakkai zasshi 1991
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Human Monoclonal ITGA2 Primary Antibody for ICC, IHC (fro) - ABIN3201578
Yun, Guan, Liu, Zhang, Wang, Qi, Cui, Liu, Zhang, Gao, Gao, Li, Gao, Wang: Integrin αvβ1 Modulation Affects Subtype B Avian Metapneumovirus Fusion Protein-mediated Cell-Cell Fusion and Virus Infection. in The Journal of biological chemistry 2016
Human Monoclonal ITGA2 Primary Antibody for IF, ELISA - ABIN561540
Haglund, Tillgren, Addis, Wenglén, Recklies, Heinegård: Identification and characterization of the integrin alpha2beta1 binding motif in chondroadherin mediating cell attachment. in The Journal of biological chemistry 2011
GPIa C807T polymorphism is associated with unexplained female infertility and IVF implantation failure
This study shows that BTK kinase takes an indispensable role in alpha2beta1 integrin signaling in platelets.
DAR1 p110 could strongly enhance the adhesion of HCC tumor cells to ECM, which was usually regarded as the initiation of tumor invasion. Such phenotype was caused due to up-regulation of ITGA2 both in mRNA and protein level.
Interleukin-4 induces a CD44high /CD49bhigh PC3 subpopulation with tumor-initiating characteristics
Carriage of a combination of mutant alleles in multiple genes including ITGB3+CYP2C19*2 or CYP2C19*2 + ITGA2 or CYP2C19*2 are possible predictors of CVE in patients after CABG
Studied the association between integrin subunit alpha 2 (GPIa) and prostaglandin-endoperoxide synthase 2 (COX-2) genetic polymorphisms in Chinese ishemic stroke patients with or without aspirin resistance.
GP Ia C807T polymorphism may contribute to ischemic stroke development in the Chinese population (meta-analysis).
The authors identified a cell surface marker, ITGA2, which marks a proliferative trophoblast progenitor compartment in the first trimester placenta that is regulated by NOTCH signalling and exhibits unique expression characteristics.
discovered that OLFM4, CD11b, and ITGA2 are proteins that are overexpressed in both primary colon tumors and liver metastasis. These are colon cancer biomarkers with autoantigenic properties.
This study demonstrated that the transactivation of FOXL2 driven by interactions between HMGA2 and pRb might exert critical effects on the metastases and EMT of chemoresistant gastric cancer. Blocking the HMGA2-FOXL2-ITGA2 pathway could serve as a new strategy for gastric cancer treatment.
The GpIa-C807T and GpIIIa-PlA1/PlA2 polymorphisms and more pronouncedly their combination are associated with increased risk of spontaneous abortions.
The allele combination of CGC from hOGG1, ITGA2 and XPD polymorphisms was significantly associated with increased odds of nasopharyngeal carcinoma.
blood platelets have a role in amyloid-beta aggregation in cerebral vessels through integrin alphaIIbbeta3-induced outside-in signaling and clusterin release
Exposure to magnesium ions facilitated hBMSC proliferation via integrin alpha2 and alpha3 expression and partly promoted differentiation into osteoblasts via the alteration of ALP expression and activity
The synonymous common variant, GPIA rs1126643, increases the long-term adverse events risk of CABG by augmenting GPIa protein expression and enhancing platelet aggregation function.
we found a significant cumulative contribution of the genetic heterogeneity of glycoproteins Ia and IIIa and platelet-endothelial cell adhesion molecule-1 and P-Selectin genes in the risk of recurrent IVF-ET failures. The coexistence of these SNPs was associated with increased IVF-ET failure risk and the more polymorphic alleles or genotypes were present the higher the risk of IVF-ET failure, especially for younger women
Meta-analysis found that glycoprotein Ia C807T T allele or the TT genotype, the Ser-allele of HPA-3 and B allele of glycoprotein Ibalpha variable number tandem repeat polymorphisms were associated with increased risk for ischemic stroke.
Data indicate no association of maternal or fetal ITGA2 C807T SNP, ITGB3 T1565C SNP, PECAM1 CTG - GTG and SELP A/C polymorphisms with fetal growth restriction (FGR).
The most common HPA genotypes among Saudis were HPA-1 a + b- (75%), HPA-2 a + b- (62%), HPA-3 a + b- (51.5%), HPA-4 a + b- (99%), HPA-5 a + b- (76.5%), HPA-6 a + b- (100%) and HPA-15 a + b + (50%). The prevalent allele among the HPA systems was (a), except in the HPA-15 system where the (b) allele was found in 52% of the subjects.
A sulfonamide-type small-molecule inhibitor of alpha2beta1 integrin decreased average platelet adhesion in individuals with the C/T807T genotype but not in those harboring C807C.
Study in a mouse model of collagen-induced arthritis identified the integrin alpha2 gene (Itga2) as an additional and novel biomarker for rheumatoid arthritis.
P15 does not directly activate integrins by binding, but does upregulate integrin signaling to enhance differentiation of both osteoblasts and chondrocytes to increase both intramembranous and endochondral bone formation.
low expression of alpha2beta1 integrin increased protein kinase B (AKT) activation and alpha-smooth muscle actin (alpha-SMA) expression. This occurred due to the instability of phosphatase and tensin homolog (PTEN) in myofibroblasts on fibrillar collagen.
Ceacam1 is essential for normal integrin aIIbb3-mediated platelet function; the disruption of mouse Ceacam1 induced moderate integrin aIIbb3-mediated functional defects.
HRG binds to alpha2 integrin through low-affinity interactions in a heparin sulfate-independent manner, thereby blocking endothelial cells adhesion to collagen I.
LG3, through interactions with alpha2beta1 integrins on recipient-derived cells leading to activation of ERK1/2 and increased migration, favors myointimal thickening
IFN-gamma induces aberrant CD49b+ NK cell recruitment and pregnancy failure through regulating CX3CL1.
alphaIIbbeta3 regulates Syk through an ITAM-independent pathway in mice and provide novel insight into the course of events underlying Syk activation and hemITAM phosphorylation by CLEC-2
the collagen receptors DDR1 and integrin a2b1 contribute to regulate GBM-maturation and to control matrix accumulation.
Synthesis and modeling of linear and cyclic KTS-containing peptides is described that leads to their use as inhibitors of integrin alpha1beta1/alpha2beta1-mediated adhesion and other antiangiogenetic activity in human serum.
alpha2beta1 integrin contributes to the pathogenesis of retinopathy. We describe a newly identified role for alpha2beta1 integrin in mediating hypoxia-induced Muller cell VEGF-A production.
Integrin alpha2 in induced pluripotent stem cells mediates their differentiation into odontoblast-like cells.
required for the migration of memory CD4 T-cell precursors into their survival niches of the bone marrow
alpha2beta1 integrin is expressed on synovial Th17 cells from CIA mice. Its neutralization reduced inflammation, cartilage degradation, bone erosion, RANKL & IL-17 levels, & the numbers of osteoclasts and TH17 cells.
the absence of integrin alpha2beta1 alleviates the effects of age related bone degradation through over-expression of collagen type I.
TNF-alpha stimulated cerebral pericyte remodeling in an alpha2 integrin-dependent manner.
observed a significant reduction in mean platelet volume, which is consistent with the reported role of alpha2beta1 in MK maturation and proplatelet formation in vivo
Blocking integrin alpha2beta1 and ERK 1/2 pathways alleviated the effects of AMBN on osteoclast differentiation.
Expression of integrin alpha2 receptor in human cord blood CD34+CD38-CD90+ stem cells determines its long-term engrafting in NOD/SCID-IL2Rgamma(c) null mice.
Flow induced alpha2beta1 activation in cells on collagen, but not on fibronectin or fibrinogen. Conversely, alpha5beta1 and alphavbeta3 are activated on fibronectin and fibrinogen, but not collagen.
both the gpIb-VWF interaction and the integrin alpha(2)beta(1)-collagen interaction contribute to platelet adhesion under high shear stress; integrin alpha(II)beta(1) makes a greater contribution to adhesion to type I collagen because less VWF is bound
This gene encodes the alpha subunit of a transmembrane receptor for collagens and related proteins. The encoded protein forms a heterodimer with a beta subunit and mediates the adhesion of platelets and other cell types to the extracellular matrix. Loss of the encoded protein is associated with bleeding disorder platelet-type 9. Antibodies against this protein are found in several immune disorders, including neonatal alloimmune thrombocytopenia. This gene is located adjacent to a related alpha subunit gene. Alternative splicing results in multiple transcript variants.
CD49 antigen-like family member B
, VLA2 receptor, alpha-2 subunit
, collagen receptor
, human platelet alloantigen system 5
, integrin alpha-2
, platelet antigen Br
, platelet glycoprotein GPIa
, platelet membrane glycoprotein Ia
, very late activation protein 2 receptor, alpha-2 subunit
, VLA-2 receptor, alpha 2 subunit
, VLA-2 subunit alpha
, VLA-2 alpha chain
, LOW QUALITY PROTEIN: integrin alpha-2
, integrin alpha 2 subunit
, integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)