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TNXB encodes a member of the tenascin family of extracellular matrix glycoproteins. Zusätzlich bieten wir Ihnen TNXB Kits (27) und TNXB Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
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Mouse (Murine) Monoclonal TNXB Primary Antibody für ICC, IHC (fro) - ABIN267551
Aufderheide, Ekblom: Tenascin during gut development: appearance in the mesenchyme, shift in molecular forms, and dependence on epithelial-mesenchymal interactions. in The Journal of cell biology 1989
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Human Polyclonal TNXB Primary Antibody für WB - ABIN521039
Hu, Zhang, Zhang, Li, Zhu, Shao, Zeng, Xu: Comparative serum proteome analysis of human lymph node negative/positive invasive ductal carcinoma of the breast and benign breast disease controls via label-free semiquantitative shotgun technology. in Omics : a journal of integrative biology 2009
Study describes a biallelic TNXB variants in patients with congenital adrenal hyperplasia due to CYP21A2 (zeige CYP21A2 Antikörper) deletions resulting in a classical Ehlers-Danlos syndrome phenotype with skin hyperextensibility, widened atrophic scars and joint hypermobility.
patients with the TNX-deficient type EDS typically have generalized joint hypermobility, skin hyperextensibility and easy bruising. In contrast to the classical type, the inheritance pattern is autosomal recessive and atrophic scarring is absent. Molecular analysis of TNXB in a diagnostic setting is challenging.
the identification of a rare missense variant in TNXB in combination with a positive family history of VUR and joint hypermobility may represent a non-invasive method to diagnose PVUR and warrants further evaluation in other cohorts
We then quantified the tenascin-X level in serum of patients and identified tenascin-X as potent marker for ovarian cancer, showing that secretomic analysis is suitable for the identification of protein biomarkers when combined with protein immunoassay.
these results suggest that mutations in TNXB can cause hereditary primary vesicoureteral reflux .
Noticeable decreased expression of tenascin-X in calcific aortic valves.
Tenascin-X haploinsufficiency was associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia
Genome-wide association study of age-related macular degeneration identifies TNXB, FKBPL (zeige FKBPL Antikörper) and NOTCH4 (zeige NOTCH4 Antikörper) as candidate susceptibility genes.
Combined analysis of tenascin-C (zeige TNC Antikörper) expression and the nodule size improved the prediction of malignancy in this patient cohort.
rs204887 itself or a nearby variant is unlikely to play a major role in the development of schizophrenia although a cumulative contribution of rare variants in the TNXB gene cannot be ruled out.
Tenascin-x is an initiator of myocardial fibrosis and ACM development via upregulation of TGFbeta (zeige TGFB1 Antikörper)(1) and downregulation of PPARgamma (zeige PPARG Antikörper).
Altered properties of the force transmission pathways of muscle due to TNX deficiency directly affect muscle function in TNX KO mice. Such effects are likely to contribute to muscle weakness experienced by patients with Ehlers-Danlos syndrome.
Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition
TNX has either a redundant or a very subtle function in the macromolecular organization in the peripheral nerve
Tnx plays a role in the regulation of cell-cell and cell-matrix interactions: Tnx-null fibroblasts exhibit weaker adhesive properties to fibronectin (zeige FN1 Antikörper) and B16 melanoma cells than do wild-type fibroblasts.
Induction of MMP-2 (zeige MMP2 Antikörper) by Tnx deficiency is mediated through the c-Jun N-terminal kinase and protein tyrosine kinase (zeige YES1 Antikörper) phosphorylation pathway.
TNX is unlikely to be involved in matrix deposition in the early phase of wound healing, but it is required in the later phase when remodeling and maturation of the matrix establishes and improves its biomechanical properties.
TNX knockout mice have mild pregnancy-related abnormalities.
localizations of Tn-X in the leptomeningeal trabecula (TB) of adult mice and in the connective tissue of the choroid plexus (CP) in the brains of mice
Tenascin-X promotes activation of latent TGF-beta1 (zeige TGFB1 Antikörper) and subsequent epithelial to mesenchymal transition in mammary epithelial cells.
mechanical analysis of collagen gels showed an increased compressive resistance of the gels containing tenascin-X, indicating that this protein might be directly involved in determining the mechanical properties of collagen-rich tissues in vivo.
tenascin-X, via trimerization and multiple interactions with components of collagenous fibrils, plays a crucial role in the organisation of extracellular matrices.
Tenascin-X is an elastic protein and the fibronectin (zeige FN1 Antikörper) type III (FnIII) domains can unfold under a stretching force and refold to regain their mechanical stability upon the removal of the stretching force.
This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene.
tenascin X pseudogene
, tenascin XB
, tenascin Y
, tenascin X B
, growth-inhibiting protein 45
, hexabrachion-like protein
, tenascin XB1
, tenascin XB2
, tenascin X