ICC/IF analysis of HeLa cells using TBLR1 antibody at a dilution of 1:150.
ICC/IF analysis of HeLa cells using TBLR1 antibody at a dilution of 1:150.
TBLR1 antibody [4F3-A8-D9]
GTX49189
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetTBL1XR1
Overview
- SupplierGeneTex
- Product NameTBLR1 antibody [4F3-A8-D9]
- Delivery Days Customer9
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID4F3-A8-D9
- ConjugateUnconjugated
- FormulationLiquid
- Gene ID79718
- Target nameTBL1XR1
- Target descriptionTBL1X receptor 1
- Target synonymsC21; DC42; F-box-like/WD repeat-containing protein TBL1XR1; IRA1; MRD41; nuclear receptor co-repressor/HDAC3 complex subunit; nuclear receptor corepressor/HDAC3 complex subunit TBLR1; TBL1-related protein 1; TBLR1; transducin beta like 1 X-linked receptor 1
- HostMouse
- IsotypeIgG1
- Protein IDQ9BZK7
- Protein NameF-box-like/WD repeat-containing protein TBL1XR1
- Scientific DescriptionThis gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016]
- ReactivityHuman, Mouse
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203