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TNNI1 encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. Zusätzlich bieten wir Ihnen TNNI1 Kits (44) und TNNI1 Proteine (13) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 49 products:
Human Polyclonal TNNI1 Primary Antibody für WB - ABIN521026
Li, Takai, Yuge, Furukawa, Tsuno, Tsukamoto, Kong, Moriyama, Narahara: Novel target genes responsive to the anti-growth activity of triptolide in endometrial and ovarian cancer cells. in Cancer letters 2010
investigated the effects of one of these mutations, K247R of TnT, on the picosecond dynamics of the Tn core domain (Tn-CD), consisting of TnC (zeige TNC Antikörper), TnI (zeige TNNI2 Antikörper) and TnT2 (183-288 residues of TnT), by carrying out the quasielastic neutron scattering measurements on the reconstituted Tn-CD containing either the wild-type TnT2 (wtTn-CD) or the mutant TnT2 (K247R-Tn-CD) in the absence and presence of Ca(2 (zeige CA2 Antikörper)+)
Data suggest that mutations in troponin C (TnC, A8V) and troponin T (TnT, delta14-TnT) found in patients with hypertrophic cardiomyopathy together fully stabilize the active M state of regulated actin (the actin-tropomyosin-troponin complex).
pathogenesis of TNNT1 myopathies
Copeptin (zeige AVP Antikörper) and troponin T measurement could potentially improve the prehospital diagnostic and prognostic classification of patients with a suspected AMI (zeige CFD Antikörper).
TNNT1 genetic and epigenetic variations are associated with HDL (zeige HSD11B1 Antikörper)-C levels and coronary artery disease.
Three homologous genes have evolved in vertebrates to encode three muscle type-specific TnT isoforms: TNNT1 for slow skeletal muscle TnT, TNNT2 for cardiac muscle TnT, and TNNT3 for fast skeletal muscle TnT.
Nemaline body myopathy Palestinian patients were found to have a novel mutation in troponin T1.
troponin T and creatinine kinase isoenzyme (CK-MB) have roles in combined renal and myocardial injuries in asphyxiated infants
Biopsy-proven acute and viral myocarditis is associated with elevated concentrations of hs-TnT.
Troponin T1 blood levels had a positive association with increased risk for hypertrophic cardiomyopathy.
Complete loss of troponin T3a, T3b and T2c activities leads to loss of sarcomere structure.
Tnnt1, Tnnt2 (zeige TNNT2 Antikörper), and Tnnt3b were conserved in the central tropomyosin (zeige TPM2 Antikörper)- and C-terminal troponin I-binding domains but the N-terminal hypervariable regions were highly extended and rich in glutamic acid in polypeptides of Tnnt1 and Tnnt2 (zeige TNNT2 Antikörper), but not Tnnt3b.
Mouse tumor endothelial cells express troponin T.
demonstrated that ssTnT deficiency resulted in significantly decreased levels of other slow fibre-specific myofilament proteins whereas fast fibre-specific myofilament proteins were increased correspondingly
the induction of Tnnt1 gene expression in adult mouse brains by ketamine may illustrate the genes involved in the metabolic syndromes observed in neuropsychiatric disorders
Data show that cardiac expression of slow skeletal (zeige MYL3 Antikörper) troponin T (Tnnt1) strictly depends on the physical interaction between GATA4 (zeige GATA4 Antikörper)-FOG2 (zeige ZFPM2 Antikörper) in the myocardium of both atria and ventricles.
This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.
nemaline myopathy type 5
, slow skeletal muscle troponin T
, troponin T, slow skeletal muscle
, troponin-T1, skeletal, slow
, troponin I, skeletal, slow
, troponin I type 1 (skeletal, slow)
, troponin I, skeletal, slow 1
, troponin T1, skeletal, slow
, troponin T slow type isoform sTnT1
, skeletal muscle slow-twitch TnT