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SEMA5A belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Zusätzlich bieten wir Ihnen SEMA5A Kits (14) und SEMA5A Proteine (12) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 95 products:
Human Polyclonal SEMA5A Primary Antibody für WB - ABIN389165
Lu, Tsai, Lee, Hsu, Chen, Lin, Shih, Yang, Hsiao, Lai, Chuang: Identification of a novel biomarker, SEMA5A, for non-small cell lung carcinoma in nonsmoking women. in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010
Human Polyclonal SEMA5A Primary Antibody für IHC (p), IHC - ABIN251583
Maraganore, de Andrade, Lesnick, Strain, Farrer, Rocca, Pant, Frazer, Cox, Ballinger: High-resolution whole-genome association study of Parkinson disease. in American journal of human genetics 2005
Sema5A is a bifunctional axon guidance cue for vertebrate motor axons in vivo. The TSR (zeige CFL1 Antikörper) domain promotes growth of developing motor axons into the ventral myotome whereas the sema (zeige SEMA3B Antikörper) domain mediates repulsion
SEMA5A gene is associated with hippocampal volume, and their interaction is associated with reasoning ability.
De novo translocation t(5;22)(p15.3;q11.21) associated with a partial deletion of SEMA5A identified in a patient with ASD (zeige ARSD Antikörper).
data demonstrated that elevated serum Semaphorin5A in systemic lupus erythematosus patients correlated with disease activity and are involved in kidney and blood system damage; ADAM17 (zeige ADAM17 Antikörper) might be involved in the release of secreted Sema5A
Multigenerational autosomal dominant inheritance of 5p chromosomal deletions resulting in Cri-du-Chat Syndrome with SEMA5A, CTNND2, and ICE1 deficiencies has been described.
The Single-Nucleotide Polymorphism (SNP) of rs7702187 within the SEMA5A gene would be a high-penetrant risk factor for PD development.
Using human gastric cancer cell lines, found semaphorin 5A significantly promoted invasive & metastatic abilities of gastric cancer cell in vitro. Semaphorin 5A increased expression of MMP9 by activating phosphorylated ErK1/2 in gastric cancer cell.
Results suggest that a bioactive, secreted form of Sema5A-ECD (zeige SHFM1 Antikörper) has an intriguing and potentially important role in its ability to enhance pancreatic tumour invasiveness, angiogenesis and micrometastases.
Data show that Semaphorin 5A (Sema5A) and plexin-B3 (zeige PLXNB3 Antikörper) inhibit glioma cell invasion through Rac1 inactivation.
The downregulation of SEMA5A in tumor tissue, both at the transcriptional and translational levels, was associated with poor survival among nonsmoking women with NSCLC.
Data represent a novel signaling of semaphorin 5A and plexin B3 in the control of cell motility by indirect inactivation of Rac1 through RhoGDIalpha.
Mouse Sema5A negatively regulates synaptogenesis in early, developmentally born, hippocampal dentate granule cells.
The results of this study concluded that the Sema5a mice do not meet the behavioral criteria for a mouse model of autism.
Sema5A and Sema5B (zeige SEMA5B Antikörper) inhibit retinal neurite outgrowth through PlexinA1 (zeige PLXNA1 Antikörper) and PlexinA3 (zeige PLXNA3 Antikörper) receptors both in vitro and in vivo.
Data reveal that Sema5A is a novel proangiogenic molecule, inducing endothelial cell proliferation and migration and inhibiting apoptosis.
development of some CNS nerves requires inhibitory sheaths to maintain integrity, this is accomplished using molecules such as Sema5A that exhibit conserved inhibitory responses in the presence of impinging signals from multiple guidance molecules.
Plexin-B3 (zeige PLXNB3 Antikörper) is a functional receptor for semaphorin 5A
Semaphorin 5A (Sema5A) is a bifunctional guidance cue exerting both attractive and inhibitory effects on developing axons of the fasciculus retroflexus, a diencephalon fiber tract associated with limbic function.
A role of Sema5A in the remodeling of the cranial blood vessels was shown.
This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A
, semaphorin 5A
, sema F
, semaphorin F
, M-Sema D