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TPM3 encodes a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. 再加上，我们可以发TPM3 蛋白 (16) 和 TPM3 试剂盒 (8)和数多这个蛋白质的别的产品。
Showing 10 out of 35 products:
Human Polyclonal TPM3 Primary Antibody for IHC, IHC (p) - ABIN4362650
Singleton, Rouhi, Zois, Haider, Li, Kessler, Cao, Harris: Hypoxic regulation of RIOK3 is a major mechanism for cancer cell invasion and metastasis. in Oncogene 2014
Human Monoclonal TPM3 Primary Antibody for IHC (p), ELISA - ABIN521063
Doukhanine, Gavino, Haines, Almazan, Richard: The QKI-6 RNA binding protein regulates actin-interacting protein-1 mRNA stability during oligodendrocyte differentiation. in Molecular biology of the cell 2010
Cow (Bovine) Polyclonal TPM3 Primary Antibody for WB - ABIN2776646
Ramsey, Clarke, Roberts, Sullivan, Johnson, Liu: An economic evaluation of atorvastatin for primary prevention of cardiovascular events in type 2 diabetes. in PharmacoEconomics 2008
Show all 2 Pubmed References
This work uncovers a Quaking/Tpm3 pathway controlling de novo myofibril assembly.
Analysis of the residual, resected tumor identified a chromoplectic TPM3-ALK rearrangement that involved many other known oncogenes and was confirmed by rtPCR.
expression levels of tropomyosin 3 (TPM3) were higher in stage III ESCC tissue compared with stage I (P<0.05). The findings of the present study identified twelve proteins, which are closely associated with ESCC invasion and metastasis, apoptosis and cell signal transduction.
Dominant mutations in TPM3, encoding alpha-tropomyosinslow, cause a congenital myopathy characterized by generalized muscle weakness. Here, we used a multidisciplinary approach to investigate the mechanism of muscle dysfunction in 12 TPM3-myopathy patients.
This work expands the phenotypic spectrum of TPM3-related disease and provides insights into the pathophysiological mechanisms of the actin-tropomyosin (显示 TPM2 抗体) complex
Western blot showed phosphorylation of ALK, ERK1/2, and STAT3 (显示 STAT3 抗体) in cells transfected with TPM3-ALK. Coiled-coil structure of TPM3 contributes to the transforming ability of the TPM3-ALK fusion protein, and longer TPM3 region leads to higher dimer formation.
Patients with TPM2 (显示 TPM2 抗体) mutations tended to present with milder symptoms than those with TPM3 mutations, DA being present only in the TPM2 (显示 TPM2 抗体) group.
in a cohort of 94 patients with congenital myopathy, 2 related female patients and 2 sporadic male patients were found to carry mutations in TPM2 (显示 TPM2 抗体) and TPM3 genes respectively; clinical presentation and muscle morphological findings differed in the patients
DATA show that tropomyosin 3 protein (TPM3) plays a critical role in the progression of gliomas.
study reports on a three-generation family with cap myopathy caused by a novel heterozygous mutation in TPM3
In addition to CLIC1 (显示 CLIC1 抗体) and TPM1 (显示 TPM1 抗体), which were the proteins initially discovered in a xenograft mouse model, CLIC4 (显示 CLIC4 抗体), TPM2 (显示 TPM2 抗体), TPM3, and TPM4 (显示 TPM4 抗体) were present in ovarian cancer patient sera at significantly elevated levels compared with controls.
Tpm3 plays crucial roles in maintaining cortical actin integrity and asymmetric cell division during oocyte maturation, and that dynamic regulation of cortical actin by Tpm3 is critical to ensure proper polar body protrusion.
TMBr-3 and TM5NM1 modestly affected actin assembly kinetics, in an opposite manner.
Tropomyosin (显示 TPM2 抗体) regulates cell migration during skin wound healing.
Data conclude that exon 9d-containing isoforms are not essential for survival of neuronal cells and that isoform choice from the gamma-Tm gene is flexible in the brain
Reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm of mice with diaphragmatic defects.
Tropomyosin 3 expression leads to hypercontractility and attenuates myofilament length-dependent Ca(2 (显示 CA2 抗体)+) activation.
tropomyosin (显示 TPM2 抗体) isoforms regulate neuronal size and shape
results indicate that a Tm5NM1-defined actin cytoskeleton is required for the normal excitation-contraction coupling in skeletal muscle
This gene encodes a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosins are dimers of coiled-coil proteins that polymerize end-to-end along the major groove in most actin filaments. They provide stability to the filaments and regulate access of other actin-binding proteins. In muscle cells, they regulate muscle contraction by controlling the binding of myosin heads to the actin filament. Mutations in this gene result in autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this locus are associated with cancer. Multiple transcript variants encoding different isoforms have been found for this gene.
alpha-tropomyosin, slow skeletal
, cytoskeletal tropomyosin TM30
, heat-stable cytoskeletal protein 30 kDa
, tropomyosin alpha-3 chain
, tropomyosin gamma
, tropomyosin 3
, tropomyosin 5
, nonmuscle tropomyosin 5
, tropomyosin 3, gamma
, tropomyosin non-muscle
, tropomyosin 3 L homeolog
, tropomyosin 3 S homeolog
, min alpha-trop