Caveolin 3 antibody [N1N2], N-term
GTX109650
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetCAV3
Overview
- SupplierGeneTex
- Product NameCaveolin 3 antibody [N1N2], N-term
- Delivery Days Customer9
- Application Supplier NoteWB: 1:1000-1:20000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID859
- Target nameCAV3
- Target descriptioncaveolin 3
- Target synonymsLGMD1C, LQT9, MPDT, RMD2, VIP-21, VIP21, caveolin-3, M-caveolin, cavolin 3
- HostRabbit
- IsotypeIgG
- Protein IDP56539
- Protein NameCaveolin-3
- Scientific DescriptionThis gene encodes a caveolin family member, which functions as a component of the caveolae plasma membranes found in most cell types. Caveolin proteins are proposed to be scaffolding proteins for organizing and concentrating certain caveolin-interacting molecules. Mutations identified in this gene lead to interference with protein oligomerization or intra-cellular routing, disrupting caveolae formation and resulting in Limb-Girdle muscular dystrophy type-1C (LGMD-1C), hyperCKemia or rippling muscle disease (RMD). Alternative splicing has been identified for this locus, with inclusion or exclusion of a differentially spliced intron. In addition, transcripts utilize multiple polyA sites and contain two potential translation initiation sites. [provided by RefSeq]
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203
References
- Böhm J, Biancalana V, Malfatti E, et al. Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations. Brain. 2014,137(Pt 12):3160-70. doi: 10.1093/brain/awu272Read this paper
- Ullrich ND, Fischer D, Kornblum C, et al. Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle. Hum Mutat. 2011,32(3):309-17. doi: 10.1002/humu.21431Read this paper





