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COL8a2 encodes the alpha 2 chain of type VIII collagen. Zusätzlich bieten wir Ihnen COL8a2 Proteine (9) und COL8a2 Kits (2) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 48 products:
Human Polyclonal COL8a2 Primary Antibody für WB - ABIN611143
De Zeeuw, Hoogenraad, Goedknegt, Hertzberg, Neubauer, Grosveld, Galjart: CLIP-115, a novel brain-specific cytoplasmic linker protein, mediates the localization of dendritic lamellar bodies. in Neuron 1998
Show all 2 Pubmed References
Human Polyclonal COL8a2 Primary Antibody für IF, IHC (p) - ABIN655804
Okumura, Minamiyama, Ho, Kay, Kawasaki, Tourtas, Schlötzer-Schrehardt, Kruse, Young, Quantock, Kinoshita, Koizumi: Involvement of ZEB1 and Snail1 in excessive production of extracellular matrix in Fuchs endothelial corneal dystrophy. in Laboratory investigation; a journal of technical methods and pathology 2015
Analysis of SLC4A11 (zeige SLC4A11 Antikörper), ZEB1 (zeige ZEB1 Antikörper), LOXHD1, COL8A2 and TCF4 (zeige TCF4 Antikörper) gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy found no evidence for found polymorophisms causing the disease in this specific pedigree.
Peripheral, anterior microcystic corneal edema represents a characteristic aspect of the phenotype associated with the p.(Leu450Trp) substitution in COL8A2, in at least 2 of 3 known affected families worldwide.
No mutations were identified in COL8A2, in neither the late-onset cohort nor the early-onset family, suggesting genetic heterogeneity in this Late-onset Fuchs endothelial corneal dystrophy (FECD) family.
mutations in the COL8A2 gene do not contribute to all cases of early-onset early-onset Fuchs' endothelial corneal dystrophy .
Variation in the COL8A2, SLC4A11 (zeige SLC4A11 Antikörper), and ZEB1 (zeige ZEB1 Antikörper) genes is present in only a small fraction of African American cases and as such does not appear to significantly contribute to the genetic risk of Fuchs endothelial corneal dystrophy.
Esophageal transcript profiling identified a distinct subset of genes, including COL8A2, in patients with Eosionophilic esophagitis and inherited connective tissue disorders.
Association of central corneal thickness with TCF4 (zeige TCF4 Antikörper) was also significant (p = 6.1x10(-7)), but was abolished with adjustment for FECD grade (p = 0.92).
Single nucleotide polymorphisms in COL8A2 gene is not associated with central corneal thickness in glaucoma.
Report cellular model in which collagen VIII (zeige COX8A Antikörper) mutations, which clinically result in Fuchs' dystrophy, are associated with abnormal cellular accumulation of collagen VIII (zeige COX8A Antikörper).
The purpose of this study is to evaluate COL8A1 (zeige COL8A1 Antikörper) and COL8A2 as candidate genes for thin central corneal thickness in human primary open angle glaucoma patients.
Overexpression of the Col8a2 gene in mouse and human Fuchs endothelial corneal dystrophy endothelial cells suggested a role for altered autophagy in this disease.
in contrast to diabetic wild-type mice EMT (zeige ITK Antikörper)-like changes were attenuated in diabetic Col8alpha1/alpha2-KO mice, indicating that collagen VIII (zeige COX8A Antikörper) may be 1 of the major inducers of epithelial-to-mesenchymal transition-like changes in kidneys of diabetic wild-type mice
study confirms the Q455K substitution in the COL8A2 gene as being sufficient to cause FECD in the first mouse model of this disease and supports the role of the UPR and UPR-associated apoptosis in the pathogenesis of FECD caused by COL8A2 mutations
Type VIII (zeige COX8A Antikörper) collagen significantly modulates the effect of TGF-beta1 (zeige TGFB1 Antikörper) on mesangial cells and may therefore play a role in the pathogenesis of diabetic nephropathy.
Smooth muscle cells can modify the matrix microenvironment by producing type VIII (zeige COX8A Antikörper) collagen, using it to overlay type I collagen, and generating a substrate favorable for migration
Lack of type VIII (zeige COX8A Antikörper) collagen confers renoprotection in diabetic nephropathy in a knockout mouse model.
The mouse mutant Aca23 described here offers the first point mutation of the Col8a2 gene and suggests that a functional collagen VIII (zeige COX8A Antikörper) alpha2 gene is essential for the correct assembly of the Descemet's membrane and for corneal stability.
This gene encodes the alpha 2 chain of type VIII collagen. The protein is a major component of the basement membrane of the corneal endothelium and forms homo- or heterotrimers with alpha 1 (VIII) type collagens. Defects in this gene are associated with Fuchs endothelial corneal dystrophy and posterior polymorphous corneal dystrophy type 2.
collagen, type VIII, alpha 2
, collagen alpha-2(VIII) chain
, collagen VIII, alpha-2 polypeptide
, collagen type VIII alpha 2
, dJ665N4.1 (collagen type VIII alpha 2)
, endothelial collagen
, procollagen type VIII alpha 2
, procollagen, type VIII, alpha 2